a aes
Sonoid %
, MERITORIOUS House of Education.
Main Campus:
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1X Chemistry
Chapter #3 INTRODUCTION TO CHEMISTRY
ON ie
? (CHEMISTRY: re
(Detinition i
“The branch of science that deals with the
properties of matter is known as Chemistry.)
psy oreo foe
( BRANCH!
or.cHemistry: (Any 5) Ny
Chemistry is digiced into ¥pllowing nine
branches:-
) Physical Chemistry, , i) Organic Chemistr
i) Phys if, i) Organic Chemistry
iv) Nugiosr Chernistrye by errata cert,
\, vii) Analytical Chemistry viii) Bio Ghemistry
iii) Inorganic Chemistry
vi) Industrial Chemistry 5
/
<) Polymeric Chemistry ¥
\ “The branch of Chemistry thatdeals jth the study of principle)that
‘governing}the combination of atoms ogmolegulesg{s known as Physical Chernistry.")
Organic Chemistry:-
“The branch of cher - tht es with the study of hydrocarbons and
3. Inorganic Chel piety
niptiy that deals with the study of all the elements:
igration and their derivatives is known a5
anid compounds excep fo
| Inorganic Chemistry”.
| 4. Nuctear eons Ne x
( f chemistry that deals with the study of nuclei, their
j he bran
{ “chanues, wegnes jpanied in those changes.is known as Nuclear Chemistry"
| cf
jal Chemistry:-
a eet of nein a stew 8 ty of changed
place Ihiko erronmenhand their offect on cis chemical conditions ofthe
nvironmipt is known ae Environmental Chemistry
WM
| 5. Epvirorl
6. indifStrial Chemistry:-
NSF The branch of chemistry that deals with the study of industrial
processes and their conditions such as synthesis of rubber, paints, fertilizers, oll et¢
14 Shis{is known as Industrial Chemistry”,
‘
I: Anelytical Chemistry: = ie
“The branch of chemistry that deals with the study of kinds of
components and determination of their values present in.a particular substances
known as Anaiytical Chemistry"BR MERITORIOUS House of Education
Park Opp: Faraan Masjid, Karachi
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1X Chem
Main Campus:
try:=
} hs manch of chemistry that deals with the study of animal ang,
fants
is known as Bio Chemistry”.
study SigigiAners is
OF CHEMISTRY:
passage of time) To study the history of ghemistny WaQave divided it into following
9. Polymeric Chemistry:~
“The branch of chemistry that deals with t
known as Polymeric chemistry”.
three periods:
i) Greek Period
GREEK PERIOD:
Che Greeks were the first one,yo stafed the work in the field of
che! Grock period along with his
chemistry, Aristotle, one of the greatg
Contemporaries explained that ever/eupstance 's made up of four basic
constituents:
S pair ~
ii) Fire
ii Eaith *
iv) Water
try,
ERIOD: - (600AD -'1600AD)
fowing are:the scientists who workedjin the field of chemistry
f Utes teh
Ef te etdof a
— Z muslis
=
Ap HAYYAN (721A. — 803A.D)
istry.
prepared compounds such as hydrochloric acid, nitric acid etcywhich '< .
fave great importance in the jabs as-well-as i the industry.
© He extracted metals from their ores which was a great achievement at thet
period of tie.
+ He gave anew era to the discoveries of chemistry and specified a direction
to the field of chemistry.
2 H.com
x
pn
Gulshan.
a ana
stueying ¢
but in doir
|HydrochtoIn
gy
foi,
he
Gulshan Campus: A-1 Bock13-c Guishane-a
Gs MERITORIOUS House of Education
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Ph: 02124940123,
1X Chernistry
AL-RAZI (862A.D — 930.0)
He has worked in the fields of chemistry, Biology and in philosophy
certain extent.
He was the fir
He used opium as an anesthesia for the very firs
He prepared ethyl alcohol by the proces:
He gave the classification of living and non-
AL:BERUNI (973A.D — 1048A.D)
tone who classified elements int
ots got non cto a
Eee
Chemistry.
Jditferent medicines.
ncentrated on the baser metals and
The Muslim Scientists were
|stuaying their properties.) Aithough they Were enable to achieve thei 1stimate goal
ii
id'ete, which have great importance in fabor:
JXLWBK : (1728A.D ~ 1799.4.D)
repared the carbondioxide gas (CO;) and studied its propertie.
iii) J. RRESELY: (1733A.D ~ 1804A.D)
iv)
v
He discovered the sulphurdioxide (SO.), oxygen (O.) anc hydrochloric
(HCl) gases.
SHELEY: (1742A.D — 1786A.D)
He prepared chlorine gas.
CAVENDISH: (17314.D — 1810A.D)
He discovered and prepared hydrogen (H:) 925.Ww <= MERITORIOUS House of Education, yy
—
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rious.com.pk
0) ht mated an este of, Webswwew.n jl
vi) LAVOISER: (1734A,D ~ 1794A.D) (-« a Naelings plenty
«He determined the percentage of oxygen gas in air. He gave a very ELEME
important law known as LAW OF CONSERVATION OF MASS re
simpler.
vii) D= JOHN DALTON: (1766A. 1844A.D) EI
* He gave all the famous theory known as “Dalton’s Atomic,Theory”, element
+ Even having some drawbacks; this theory gave @ new direction to
Reeeren erie. CU
GENERAL DESCRIPTION: they fon
In this period several achievements have been observed through mM
different scientists. Rutherford and Neil Bohr giving their atomic models. identity.
Radioactivity is the another phenomenon of high appreciation which was being they give
discovered. aa
CONCEPT RELATED TO EXPERIMENTS: “V
Sat: then the
OBSERVATION: i) Inc
‘A group of data collected after performing several experiments is know, '!) Ele!
as Observation. Observation is a very rough calculation to a certain approach, iii) Spe
ace
HYPOTHESIS: iv) Cor
Hypothesis is an idea which the scientists derive from their
observations. It is very much imaginary and it could be amended anytime. MIXTUF
Hypothesis is next step to observation. y
they forr
THEORY: . ) Ina
Theory is a statement which is also a result of observations taken from il) Ele
the experiments. Theory is less flexible as compared to Hypothesis. Itis basically iii) Sim
next step to Hypothesis. my
LA iv) Mix
a i v) Mix
The next step to theory is known as Law. It has got maximum evidence 1.
as compare to theory, hypothesis and observation. It has derived from a number of
practical experiments. HOMO
“t
+ Hor
Chapter # 2 CHEMICAL COMBINATIONS thei
BASIC CONCEPTS OF CHEMISTRY: ° Exe
ATOM:
“The smallest particles of an element is known as atom”
. ___ Atom is the fundamental particle which is the basic concept of chemistry.
itis a hypothesis that atom constitutes all the substances which are known as matter, eler70N4) MERITORIOUS House of Education
otmaiie, Main Campus: 17, PIs Colony, Near K.M.C Park Opp: Faraan Masiid, Karachi Z
chi “Ph: 021-34940423, 0300/0921 -6232196, e-mail: meritorious.
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mistry Web:waw.meritorious.com.pk
1X Chemistry
ELEMENT:
lement is the smallest substance which cannot be broken down into
simpler substances.”
Element consists of a large number of atoms. Ina little amount of an
element there could be thousands of atoms.
MOLECULE:
When two or more than two atoms chemically combine together then
they form a molecule.”
Molecules are composed of several atoms. These atoms lose their
identity when they form a molecule. When several molecules combine together then
a they give rise to a compound.
COMPOUND
“When two or more than two elements chemically combine together
then they form a compound.”
i) In Compound elements lose their individual properties
known |) Elements could not easily be separate from compounds
i it) Special chemical processes are required to separate constituent elements from
a compound.
iv) Compounds can be represented by a chemical formula
MIXTURE:
“When two or more than two elements physically combine together then
they form a mixture”.
i) Ina mixture elements retain their individual properties.
n from i) Elements could easily be separated from mixture.
“ally ili) Simple physical properties are required to separate constituent elements from a
mixture.
iv) Mixture can not be represented by a chemical formula.
v) Mixtures divided into following two types.
dence 1. Homogenous Mixture 2. Heterogenous Mixture
ber of
HOMOGENOUS MIXTURE:
“A mixture having uniform composition is known as Homogenous Mixture.”
. Homogenous mixture does not have visible boundaries of separation between
their elements.
+ Examples of Homogenous Mixture are sugar solution, salt solution, air ete.
HETEROGENOUS MIXTURE:
“A mixture of non uniform composition is known as Heterogeneous Mixture”.
ry: + Heterogeneous mixture has visible boundaries of separation between their
5 matter, elements.
+ Examples of Heterogeneous Mixture are mixture of iron and sand, mixture of
sand and salt.~—* MERITORIOUS House of so
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‘hem,
‘sty
ATOMIC NUMBER: i:
"The no. of protons present in the nucleus of an atom is KNOWN as Atomic
Number.” .
itis represented by Z dicate
For example: Atomic Number of Carbon is 6 which shown it has 6 protons ,,
its nucleus eval
i
VALENCY: 5 ”
"The combining power of an element is known as its valency”. :
SYMBOLS OF ELEMENTS: iv)
S.No| Common Names Latin Names Symbols
01 | Hydrogen -] H
02 | Helium =f - te maleut
03 | Lithium = = Li be
04 | Beryllium E ‘i Be
05 | Boron Ss 3 i
06 Carbon a
07 | Nitrogen i-
08 | Oxygen 5
09 | Flourine molecule
10 | Neon i
11_| Sodium fe iy
12 | Magnesium fe a
13_| Aluminium (ee Z MOLE:
14_| Silicon el
15 | Phosphorus _ aa i
16_| Sulphur Pi : e ii
17_| Chlorine i iy
18
_19 | Rota FORMU
20
21
ee The Uni
AVAG:
Atomic No. | Name of Elements | EV
1 Hydrogen H iF
2 Helium [a teHe.
3 Lithium [ian ORM
4 | Beryllium Be g
5 Boron
6. | Carbon
Ei Nitrogen BALAI
é ()
9O;
*) MERITORIOUS House of Education
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om Ph: 021-34540123, 0300/0321 -8232196, e-mail:
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1X Chemistry
3 ATOMIC MASS:
“The mass of an atom measured in comparison with the mass of
standard C" (Carbon 12) is known as Atomic Mass” — OR af
ONS in
“Th sum of number of protons and neutrons present in the nugloygof
an atom is known as Atomic Mass” g
Ww
i) Atomic Mass is also known as “Mass Number” | “| a
ii) Itis'measured in atomic mass unit (a.m.u) -
iii) The atomic mass of oxygen is 16 a.m.u
iv) The atomic mass of hydrogen is 1 a.m.u
MOLECULAR OR ACTUAL. FORMULA!
“The formula that represents actual ratio among the atoms ina
molecule is known as Molecular Formula”.
i) The Molecular Formula of Glucose is Cs H;2. Ov.
ii) The Molecular Formula of ethane is C3 He.
EMPERICAL FORMULA:
“The formula that represents simplest ratio amoung the atoms ina
molecule is kiewn as Emperical Forma”
i) The Emperical formula of glucose is CHz0.
ji) The Emperical formula of ethane is CH3.
= MOLE:
“Gram atomic or. gram molecular mass of a substance is known as Mole”.
i) 1 mote of NaCI contains 58.59.
ji) 1 mole of H20 contains 189.
2 iii) 1 mole of H2SQ« contains 98g.
FORMULA:
Mole = Mass in gram
Atomic / Molecular Mass
The Unit of mole is mol.
AVAGADRO'S NUMBER:
1 mole cf any substance contains 6.02 x 10” particles. This is known
as Avogadro's number.
“It is represented by Na
FORMULA: .
- No. of particles = No. of moles x Na. OR
No. of particles = No. of moles x 6.02 x 10”
— BALANCING OF CHEMICAL REACTION.
a (a) NajSO,+H20~___* NaOH + H2SO4
The following data can be used from this equation.
9
we ieee” © meriroriovus House of Educatiox) yy
2
Main Campus: 17, Pip colony, Near KM P napa kt ese
po. 7¢ Rim Coteny, Nene regaat #232108, eal: mertorious_pb@hoind Main Cs
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ulahane aeszige, email: meritorious. guishen@hom Gulshan
rk Opp: Fara
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ag IX Chemis,
REACTANTS I PRODUCTS
Na: 2 Nad
i S:1 i Sit ’
0:5 joree i= ia
He I eee standard
Inthe above chemical reaction Sodium and hydfagen are ynbal .
ic jium in tHe produ Spare
We use a coefficient 2 before NaOH to balance Sod} @ product ;
Walco) io 2 NP AN i
“REACTANTS PRODUCTS _ iii
j Na: 2 = = Ky
— i aban _
= ze ate ——
ie Fagmanrea nee
Now for balancing hydrogen we use 2 before H,0 In the reactant size, motacule
NazSO, + 2H20 = 2 NaOH H2SO« i
— i)
__REACTANTS
- :
[ % molecule
is completely balanced. i
Hence the above chemical Equation
CHEMICAL REACTION: ‘*
shemical chang,
“When one or twéithan one substances undergoes 2 C!
‘ha process is known as )
and produce one or more than’one substances then suc!
$4 i)
Chemical Reaction”.
iii)
s 4
CHEMICAL EQUATION:
help of chemica; FORMU,
3
~ = oo
Fngrepresentation of chemical reactions with the
rom thBreactants and products is known as Chemical Equation”.
», ¥
The Unit
\IYPES OF CHEMICAL REACTIONS:
“There are seven types of Chemical Reactions which can be reduced avaGa
five types,
in@fPadition or Synthesis
ii) Simple Decomposition
iii) Simple Displacement
Double Displacement. (Neutralization, Hydrolysis) FORMU:
as Av
%
iv)
v) Combustion
1. Addition or Synthesis:
BALAN
“When two or more than two substance combine together and form;
single product then the reaction is known as the Addition or Synthesis Reaction. (2)
10itioZ)
—
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IX Chemistry
g ATOMIC MASS:
“The mass of an atom measured in comparison with the mass of
lé standard C"? (Carbon - 12) is known as Atomic Mass" OR af
“The sum of number of protons and neutrons Present in the nucleus of
: an atom is known as Atomic Mass” 7 \s
1) Atomic Mass is also known as “Mass Number” Pa
ii) Itis measured in atomic mass unit (a.m.u) ; ¥
iil) The atomic mass of oxygen is 16.mu Ns
v) The atomic mass of hydrogen is 1 a.m.u
duct sig
MOLECULAR OR ACTUAL FORMULA!
“The formula that represents actual ratio among the atoms in a
fant size, molecule is known as Molecular Formula”. ‘
i) The Molecular Formula of Glucose is CsH:2.0s- )
ii) The Molecular Formula of ethane is Ci Heo.“
EMPERICAL FORMUL.
“The formula that represents simplest ratio amoung the stoms ina
olecule is kriown as Emperical Formula”.
i) The Emperical formula of glucose is CH20.
ii) The Emperical formuta of ethane is CH.
MOLE:
-al chang, “Gram atomic or.gram molecular mass of a substance is known as Mole”.
1OWN as i) 1 mole of NaCI contains 58.5g.
ii) 1 mole of h,0 contains 18g.
iii) 1 mole of H,SQ, contains 98g.
hemicay FORMULA: 5. “i
} Mole’ Mass in gram
“seal Atomic /Molecular Mass
The Unit of mole is mol.
NUMBER:
gf mole of any substance contains 6.02 x 10” particles. This is known
as Avogadro's number.
“itis represented by Na
reduced VAGADRO'
FORMULA: ,
No. of particles = No. of moles x Na. OR
No. of particles = No. of moles x 6.02 x 10”
ind formyBALANCING OF CHEMICAL REACTION
Reaction” (a) Naz2SO4+ H20 NaOH + H2SO4
The following data can be used from this equation.
9<% MERITORIOUS House of Ecucatio,»
~~ M
1 K.M.c Park Opp: Faraan Masjid, Karachi
MPa Fe e-mail: MerOriOUs PIDDrotmyy x4.
SD tai
atop, Federal Urdu University, Karagy) | Matis C3
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1X Chemig,
REACTANTS | __ PRODUCTS
feet t - Examples
| Sif S1 5 ampl
O:5 t 0:5
Hz I 4:3 as |
Inthe above chemical reaction Sodium and hydfogen a7 ynbal
at
We use a coefficient 2 before NaOH to balance Sodjtim in th product sig2, Simpl
Roo 2ngon gis. ft ee
oe pexcTANTS | PRODUDTSS YW we,
__Na:2 i ss
[eS af Examples
L 9:5 =
mez! = a
how for balancing hydrogen we fise 2 before Fiz0 in the reactant sizq
Na;SO. + 2H,0 —___—»_ |? NaoH+ H2SO4
. 3. Simple
recause o
Reaction”
Examples
CHEMICAL REACTION:
“When one or tw6 thar
or more than/one substances then such a process is known ag
none substances undergoes a chemical chang)’-2Oubl
and produce one
Chemical Reaction”. 18 ach other
3 displacem
CHEMICAL EQUATION:
xamples
3
Figseherrensaton of chemical reactions with the help of chemica,
formulalof there: ene and products is known as Chemical Equation”.
\TYPES OF CHEMICAL REACTIONS:
“There are seven types of Chemical Reactions which can be reduceg,
five types, leutraliz
i@fAddition or Synthesis é
ji) Simple Decomposition uch area
iii) Simple Displacement xamples
iv) Double Displacement. (Neutralization, Hydrolysis)
v) Combustion
1. Addition or Synthesi
“When two or more than two substance combine together and formdydrolys
single product then the reaction is known as the Addition or Synthesis Reaction"17, PIB Colony, Noar K.M.C Park Opp: Faraan Masjid, K
chi
021-34940123, 0300/0321 -8232196,
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IX Chemistry
Examples
sD SHeeke * 2NHs
ii) C+ 2H, * CH.
iii) Ca0 + CO, *caco;
adiuct sig2. Simple Decomposition \e
“When a single reactant is broken down into tw
9 or more.products by
eating it or using some other methods is known as SimplalDecomp: pion Reaction
a qv
Examples 7 ‘
i) Caco, —* CaO coz f }
ii) 2KClo, * 2KOf +30;
tant size iii) Ca (OH)2 — —» CaO0+H,0 ‘
\
3, Simple Displacement:
“When an atom or a group of atom replaces’ another atom or group of atom
ecause of electro negativity or electro positivity is known as Simple Displacement
Reaction”, hue)
Examples: } ss
i) 2HBr + CL; ———> ‘2HCh+Br,
ii) ZnChz+ 2Na_ —> “wgnack + zn
iii) Ca (OH)2* 2K —* — 2KOH+Ca
_ 1. Double Displacement:
sal chang, C¥“e Sisplacement
10wn ag “The reaction in which two different atoms or group of atoms replace
ach other or interchange each other then such a reaction is known as Double
displacement Reaction”
amples:
‘hemical i), CaC6s+NazSO, —— Na,CO; + CaSO,
ii) MgCiz + 2Na NO; + Mg(NOs)2 + 2NaCL
ili) 2KBr + Zn(HCO:). ———* 2KHCO; + ZnBr2
Double Displacement Reactions can be classified into:
leutralization
e reduced
gi “When an acid reacts with a base then it produces salt and water and
uch a.reaction is known as Neutralization Reaction”.
xamples: :
NaOH +HCl_ —————* Nac +H,0
ii) Ca@GH)2 + H2SO, —____, CaSO, +2H20
iil) KOH + HNO; ——___+ KNO,+H,0
and forma ydrolysis:
Reaction", “When a salt reacts with water and produces acid and base then it is
known as Hydrolysis”.
it
mr a errr creerW & meritorious Hous
e of Educatig,
woieinn K
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Main Campus: _ 17, PIs Colony, Near KW. c Park Opp: rarean Mees nt I
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TX Chemiy
Examples:
i) ZnChz + 24,0 ————* Zn(OH)2* Bul °
noe ee Esse Pj explana
NON OD eC a aa sot HCO A,
y - \ called a"
5_COMBUSTION: 4 with HCl
cWhen a substance react with oxyge” atgomospish temdePeture te noted do
produce oxides Is known as Combustion Reaction” \e ne
Py
Examples: f I
Examples! 14,420, ———>_CO:* 210 Nae ' Equstio
)CRCH =. emaenies
iii) 2CcHe + 502 ——> 4CO; +/6H20
fy 4Nat Or ——» 2N220 WO Ny Conelu:
eo, * =
LAW OF CONSERVATION OF MASS: aan
DIAGR:
STATEMENT: at
“matter can neither be created\nor be destroyed”
WOR ©
she total masg,of reactanis 1s always equal to the mass of products
2
EXPLANATION:
i) Burning of Carbon: ><
“When carb6h stich as coal is combusted then only ash is left behing
use the remaining coa,
The mass of ash is less than the mass of coal. This is becat
has been conyert@¢h tojarbondioxide (COz), hence the mass of ash and the mag
of carbon oiveote total mass of coal.
a
c#o, — co:
i >
ii) Rusting of Iron: STATE
£ piece of iron when gets rusted becomes heavier than the original «)
piece. Thigis because of addition of mass of oxygen to that piece of iron. ersniss
2Fe +0, > 2FeO EXAMI
: aes
LANDOLT EXPERIMENT: (VERIFICA TION) Mater
Introduction: in labo
js Fe
E This law was the presented by German Chemist H. Landolt for a
verification of faw of conservation of mass. ;
: . M
12tig.
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1X Chemistry
’
| Explanation:
In this experiment an H. Shaped tube is used one arm of this tube wi
\ called ‘A’ and other arm was called ‘B’ ~ ‘A’ was filled with AgNO; and ‘8 was fiffed
“] with HCI. The'whole apparatus is shown above. Now, its masgwas measu' nda
tureto. noted down, Now, the tube was shaked and its mass was m sivas ging The mass
before and after the process was equal. ~
; Mad Ne
Equation: 3
Equation: ‘
The white precipitates of AgCl reflected the chemical reaction as:
AgNO; + HL ——». AgCI+ HNO3 i
White ppt
Conclusio:
Thus, total mass of the substance before.reaction is equal to the total
mass of the substance after reaction. oe
DIAGRAMATIC REPRESENTION: 4 ~~...
‘products
left behing
sina |
nd the mas “\e \
LAW OF CONSTANT COMPOSITION:
STATEMEN:
“Different samples of same compound always contain ‘he same
he original eiements combine together in the same proportion by mass”
on.
EXAMPLES
Water:
Water is obtained from sea, river, ponds, lake rain and can be prepared
in laboratory and its ratio can be conserved which may be shown as:
Formula H20
Mt for Elements +0
Atomic Ratio a3
Mass Ratio 2gm : 16gm OR 1gm: 8gm
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Chem
2, Formatic
1rago} 2
Cal nat
Bomate: niche usually found astimestone, marble calcite, 8 sgonig
obtained through different sources and its ratio can Be conserved which cary \comPound
shown as: Water (HC
Formula CaCO; , \tydrogen
Elements Calcium + Carbon + Oxygen Chg MH)
Atomic Ratio 14:3 oe zo ere Wee
Mass Ratio 4ogm : 12gm: 48gm ¢ Ne
z ?
ILLUSTRATION OF THE LA Gl
This Law was first justrated by Swedis#Chemist J.J Berzelius CONCLL
Berzelius illustrated the law by heating Jead (Pb) and sulphur (S) in aes
different composition. f ) ionitenen
pbs gn oe
11.56 :
11.56 + 8g of Pb remained tipused. STATEN
11.56 + 1g of Siremained unused. ae
LAW OF MULTIPLE PROPORTION: he ee
Ea a ee er
STATEMENT: e y EXAMPL
varewo elements EBmpbine to from more than are compounds, the iy c
masses of one element that combine with a fixed mass of other element are in th, P
Je ratio” | :
ratio of small whole numbers.or simple multip|
3% q
ts
EXAMPLES:
1. Formatiot por CO and CO;
[ Broun [mass of Carbon (C) | Mass of Oxygen (0) “Ratio of Oxygen
|_Carbon Monoxide (CO) 12 16 1
| Carbon dioxide (CO2) 12 32 2
Here we can see that the mass of Oxygen varies. |
ie 16:32
1:2
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IX Chemistry
tion of HO and H;03:
ragonit, :
carts {Compound | Mass of Hydrogen (H) | Mass of Oxygen (0) |
Water (H20) | 2 16
\Hydrogen Peroxide A |
a (H20) /
Here we can see that the mass of Oxygen varies
ie. 16: 32
1:2
jus CONCLUSION:
r (S) in Thus, in all the compounds if mass of ofieatom is fixed and the other
atom show a simple whole number ration. } A
LAW OF RECIPROCAL PROPORTION:
a he ee
STATEMENT:
“When two different elements\separately combine with the fixed mass of
the element, the proportions in which they combine with ‘one another shall be either
in same ratio or some simple multiple of it”.
EXAMPLES.
s, the i) Carbon and Oxygen separately combine with Hydrogen to form CH, and HzO
are in the respectively. The reciprocal ration of the above two elements is also
presented between Carbon and Oxygen in form of CO2.
ii) Carbon and Sulphur separately combine with oxygen to form COz and SO2
respectively in a simple ratio. The reciprocal ratio of the above two elements
is also presented between Carbon and Sulphur to form CS2.
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IX Chem,
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Chapter # 03 :
2
Arrcor
OLD DEFINITION: cif
“All mater consists of very small indivisible partic! les aise toms:
Z i Definitios
MODERN DEFINITION: ¥. ‘ oy 2 1
“Atom consists of other sub-atomic particlesealle tron, Proton a
and Neutron” |
: DALTON ATOMIC aa
| INTRODUCTION: Pe a, apes
Hl “This theory was presented by an£nglish ScHoo! teacher john Dat
! 1808". om ‘Charact
pe
SIGNIFICANCE: aa
| “This theory explain the chemical rd of matter and existance of _ iii)
atom”. e{s iv)
7 > : v)
MAIN POSTULATE: nf
“This theory wal based on the following points. PROTO!
i) - Matter is composed of tiny indivisible particles called atoms. feats
ii) Atoms can neither béigreated nor destroyed in chemical reaction, _ petinitic
iii) Atoms of a given elements are identical in size, shape, Mass and all othe
iscove
properties.
iv) Atoms of morgithafione element combine in a simple whole number rati
MODERN ATONNc THEORY:
7) } Atom i8a,cdmplex organization consisting of sub-atomic particles calfeg,,
Protons and Neutrons... Zharact
i
be created destroyed or charged.
oms'6f same elements are identical in size, shape and chemical ii)
préperties but they may differ in their atomic masses. Such atoms of an
iment_are known as Isotopes.
iv)xg@lAtoms of one element can be changed it
process of radioactivity.
¥) Atom (matter) can be converted in to Energy
E=me*
vi) The fate between atoms of different elements in organic compound is ppotints
simple.
into atoms of other element by the
by Einstein’s equation,
discov
16Atig~ 4
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1X Chemistry
4 FUNDAMENTAL PARTICLES OF ATOM:
\ELECTRON:
toms"
° Definition: , ¢|
, It is negatively charged particles moving
DIAGRAM REPRESENTATION: as sub at
STRUC'
cathode |
DIAGR/
~
WORKIN
WORK
i) The circuit is completed and potential difference is created. At this mom jy
___ nothing seems to be happened in discharge tube.
ii) The pressure inside the tube is reduced constantly. 0
iii) At very low pressure cathod rays can be observed moving from cathode
to anode.
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1X Chemistry
PROPERTIES OF CATHODE RAYS:
)) These particles are negatively charged,
A ii) These rays are parallel to each other.
iil) They rays can produces shadow of non-transparentt™
e iv) They have mass equal to mass of electron (1/1837 of lighter,than hydrogen
atom) } B
3CTRg ov) ‘The charge to mass ratio (e/m) is equal to e/m of electron (¢ 76 x 10°
pag ate sta PES
; y )
of elecyCONCLUSIO! ? ?
The existence of cathode particles is independent to the/nature of gas
present inside tube.
The properties of cathode particles are also independent to the nature
pe. of metal of electrode.
“Electrons are the sub atomic particles of all atom”
») and b
ANODE RAYS EXPERIMENT
ecrease
SIGNIFICANCE:
This experiment provides a confident evidence of existence of protons
as sub atomic particles.
STRUCTURE OF DISCHARGE JUBE:
Point 1 to § same as cathode rays experiment. The electrode serving as
cathode is perforated (having pares) in structure.
DIAGRAM REPRESENTATION:
WORKING:
tthismom j) Circuit is completed and pressure inside the tube is reduced. At this stage
cathode rays appear between electrodes.
ii) The gaseous atoms present between electrodes are ionized due to cathode
particles. These image particles flow toward perforated cathode and pass
through the canals of cathode.
m cathodeVv
eda e.
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ix Chey
PROPERTIES OF ANODE RAY:
i) These particles are positively charged. DARN
i) These rays are parallel to each other: ’ eee
iii) These rays can also produce shadow of non transparent object. U
iv) They have mass equal to mass of nuclei of different 8
Wy) The charge of anode particles is equal fo mute chargé of proton
CONELUSION: Ng yo \
These anode rays consist of particles identiedl © proton of atom,
“protons are the sub atomic particles of cell atoms: ‘gpd wpresent }ejatomic ny
(z) of an element
DISCOVERY OF NEUTRON OR/CHADWICK EXPERIM)
OBSER\
INTRODUCTION: . aS :
The total mass of the proton and electron i” each atom is not sure
to account for the atomic masses of different elements. This shows that there y i
rh : ii
iil)
be another heavy particles in the atoms!
BY
DISCOVERY: ?
. In 1932, James Chadwick discover neutral particles called neutron as PERU
result of artificial radioactivity. )
«He bombard Alpha péfticlas on the beryllium atom fo produce neutron, ii)
‘Alpha ~ particleS'Beryllium atom + Carbon * Neutron WD
2 + sBe® p eC"? + on" s ey
CHARACTERISTICS?
7) This patticle haSheutral nature. PRAWE
(0% kg) |
Its mass, equal to the mass of proton (1.67 x 1
7)
RUTHER FORD ATOMIC MODEL
aa
SIGNIFICANCE:
§Rutherford represents an atomic model i.e. mutual position of sub.
atomic pafticles
EXPERIMENT:
Arrangement:
Rutherford arrangement following apparatus in a sequence.
An alpha gun for firing of alpha particles.
Slit to check the path of alpha rays. IMPOR
)
Gold foil —~» acting as barrier.
Fluorescent screen ——> made of zinc sulphide to check destination
ii)
@particles. (Diagram)
20Ca
vi
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1X Chemistry
DIAGRAM RERESENTATION:
2 {
ct u
f pOton,
*
e
f atom,
tomic ny
-RIME, “
not sup 2ESERVATIONS: ‘ 3
3) Most of the alpha particles pass through gold foil without any deviation.
ii) Few alpha particles were deviated slightly from this original path.
iii) Very few alpha particles were completely deviated.
at there m
tron ag PESWLT:
utron
*8¢ i) The major portion of an atomis empty.
ii) The total mass of at n nucleus.
oneume y) ss of atom is present in nucleus.
ii) The size of the nucleus is very small as compared with the size of atom.
iv) The positive charge is concentrated in the nucleus.
v) The electron anode around the nucleus.
DRAWBACKS (DEFECTS)
According to classical Electromagnetic theory,
i) _ “Electron'will'lose energy continuously during its revolution and
| ultimately it will fall on the nucleus which will result in destruction of an
© atom."
ii) \[f electrons are losing energy continuously then continuous spectrum
on of sub. should obtain but the spectrum produced is the line spectrum.
+ Neutron
BOHR’S ATOMIC MODEL
SIGNIFICANCE: :
This atomic model provides solution for the defects present in
oe Rutherford's atomic model.
IMPORTANT POSTUCATES:
Electrons revolve around the nucleus in specific pathways called orbits or
destination energy level.
ii) During revolution around the nucleus electron does not emit energy and its
energy remain found.
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1X Chem,
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con itjumps to a higher and stdcle,
ectri
‘ack to its original orbit.
iii) When energy is provided to an ©
(iskes the axiraervouncorensiay "607
iv) Each line in spectrum represents 07 orbit which is produced due to, OBSEF
downward jumping of electron. The a7rou"™ of energy radiated is ebjuay '* 25 ©
difference of energies between orbits: z J = Som
Ieneray of lower orbit is Ey, and higher orbit is E; thoneie | + Som
Echv s + Som
v) The angular momentum of an electron revolving around ieucletis is eqy
integral multiple of reduced Planck's constant. CONC:
mVr=oh F) > The
22 f call
where, + The
m=mass of electron call
V= Velocity of electron + The
r= Radius of orbit 5 nat
n= number (1, 2, 3,4)
h=Planck’s constant ag 3
h Al
RADIOACTIVITY:
~ 2
nF Alpha
DEFINITION. ;
"The elements ha¥ing atomic number greater than 82 spontaneously ey like he
radioactive rays. These eleme! 8, are)known as "RADIOACTIVE ELEMENTS" ang they h
phenomenon is called RADIQACTIVITY.” ee
EXPERIMENT:- --
The h
Apparatus:. »
y, sed in which vacuum was present. Alead| charg
In this expérimeht.a’chamber was u
cavity was drilled. In this cavity a radioactive element was
was us
placed &nd ap eléétric field was applied across it. A photographic plate was
placed infront ofi
Their
is mi
2em
22atic.
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IX Chemistry
sudde,
it
e OBSERVATION:-
s ogy it was observed that:-
+ Some rays deflected towards the negative side of electric field.
NE] + Some rays deftected towards the positive side of electri¢ field ‘
m = Some rays continued on their path without any deflection.
is 8
g’Seq4 CONCLUSION:- % ff
+ The rays which were deflected towards the negative)side of tha field were
called as alpha rays and they had positive charge on them.
+ The rays which were deflected towards the positive side of the field were
called as beta (/3) rays and they had negative charge on them.
+ The rays which remained undeflected were called a3\gamma () rays they were
natural. 4
PROPERTIES OF ALPHA BETA‘AND GAMMA RAYS.
ALPHA RAYS | BETA RAYS” | GAMMA RAYS _ |
: () NATURE 2 a
T T
Alpha particles are just Beta’particlé is just like | | Gamma rays are
eously ey like helium nucleus i.e. We electron. | electromagnetic waves.
es they have two protons |
and) and two neutron. | |
The have positive | They have negative | __They are neutral waves.
nt. Aleaq| charge. charge. \
ent was, a Les = 4
wes 8 E ie
tT (3) SPEED \
ae =r —o— 4
Their speed is 1/100 Their speed is 1/10 \ Their speed is equal to |
time's the speed of | time's the speed of | speed of light.
light. \ ight. : |
PENETRATING POWER
Their penetrating power| Their penetrating power\ Their penetrating power|
is minimum which 1 to is greater than alpha | is maximum.
2 cms inair. | rays but less than \
| gamma rays whichis 3. |
to 4 min air. \ \
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1X Chem
- () IONIZATION POWER =
e Their ionizatio, sea
Alpha rays have the Their ionization power ic me
oa Kk n is greater than gamma is minimum.
rays. 2 . {
ae = CA © h285, 236
a ee ne (
pena = O} GHARACTERISTIC EQUATION Bs.
2.
ty}
number but different may
DEFINITION:- ; i
The atoms of same elements having similar atomic nur
number are called ISOTOPES.” ey ae |
ISOTOPES OF HYDROGEN:-
There are three isotopes of hydrogen” e
1, Protium. 8 ¥)
2. Deutrium im - vi)
3. Tritium - ;
Protium: e, > Cees
® “The isotope of hydragen which contains one proton and one electron THE F
no neutron is called PROTON.”
« _ Protium has nogtomic number of one and mass no of one aswell, DEFINI
+ Z=1and ee a
groups
,
Deutrium:- %
of The, SBtope of hydrogen whic!
| one.néiifron called DEUTRIUM.”
+ \\the atomic number of deutrium is one and its mass number is two.
Z
3 1 andA=2
fh contains one proton and one electron ;
AL-RA
DOBE!
"The isotope of hydrogen which contains one proton and one electron,
two neutrons is called TRITIUM."
+ The atomic number of tritium is one and
Z=4andA=3
Introdu
its mass number is three.
masses
Stater
ISOTOPES OF OXYGEN:
. There are three isotopes of oxygen.
20% 407 407 equal t
: al
Oxygen atom has also three isotopes having mass number 16, 17, 18. 4
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Chemj
IX Chemistry
There are three common isotopes of Uranium with numbérs 234,
235, 236 respectively.
sy nl U5 5
; = s
3 4 ELECTRONIC CONFIGURATION:
‘ ‘
— DEFINITION: .
i) “The arrangement of electrons around the nucleus of an atofn in different
characteristies shells is called electronic Configuration”.
ji) The circular orbit are designated asd K, L, M, N»O, P orbit and represented
>rent mag 3
by1, 2, 3, 4, 5, 6 starting from 1 nearest to the nucleus.
iii) The maximum number of electrons in the given shell is governed by the
formula: 2n? ‘ a
Where, n is the number of orbit (shell or energy level)
iv) The first orbit can have maximum of 2electrons (n = 1)
v) The second orbit can have maximum of & electron (n= 2)
vi) The third orbit can have maximum of 18 electrons (n = 3)
Chapter #4 PERIODICTY OF ELEMENT
electron; THE PERIODIC TABLE
well. DEFINITION:
Itis a table in, which elements are arranged into different periods and
groups according to théir atomic numbers.
» efecto PERIODIC CLASSIFICATION:
: AL-RAZI CLASSIFICATION:
istic | “According to Al-Razi,
“There are two classes of elements, metals and non-metals.”
DOBEREINER'S TRIAD:
e electro
"introduction:
A scientist, Dobereiner, classified elements accor:
ing to their ato
three. asses and presented a group of three elements known as triad.
Statement:
He stated that:
“In a group of three elements the atomic mass of middle element is
equal to the average of atomic masses of extreme elements”.
16, 17, 18.
Example:
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x Chem
4% Triad: 7
Elements AtMass ~ asd
Lithium 7” + Men
Sodium 23 7239"23 eg.
thi
Potassium 39 + Men
2! Triad . cy vale
Chlorine 35. * . The
Bromine 79.9 a5.cmegee= Ne Hi
Iodine 126.9 < d oe iE + Ele
This law is not applicable to all the ‘elements me” itis discarded. ps apy,
NEWLAND'S OCTAVES i 4
els ) Me
Introduction: ii) Ifel
ere = Ne onaerérincFbasing atomic masses,
Newland arranged elements in
6 3
Statement: /
eat periodically once after each eig
He stated that:
“The properties of elemelits Pp
element according to increasing atomic masses”. ie
s Au
iv) Lai
Example:
First three octavesare given below:
ai dise. \Seaggrks p10!
(Naw MoiwAlegasioe > ©
cro K Ca & Sti mn Fe
T does not reseffible\C and Si
Mn does not resentple N and P
Fe does not resemble S and O
, i foto all the elements the
ow o" is not applicabl
, “ 4 MENDELEEV’S CLASSIFICATION
MENDEL nereasi
,
INTRODUCTION: a
in order of increasing atomic mass!
‘Mendeleev classified elements i
and pregented “Periodic Law”.
STATEMENT:
He stated that:
“The properties of elements are perio
refore it is discar
mene
sumber
dic function of its atomic mas
SROUI
ments which were not i)
ADVANTAGES:
; Mendeleev left vacant spaces for the ele!
discovered at that time.
ii)
© On the discovery of noble gases it is found that they posses same prope
; iii)
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1X Chemistry
as described by Mendeleev.
+ Mendeleev corrected the atomic masses of different elements.
e.g. He corrected the atomic mass of Berrylium and placed it between
lithium and Boron.
+ Mendeleev described the group number of each element as the maxirhugy
(a valency of an element, *
a + The properties of elements of group I, II, Ill ete are simijar to Keletberie of
elements of group I, II, IV etc respectively. i
+ Elements exhibit periodic properties according to inereasin: ic masses,
‘ded. DISADVANTAGES: }
Mendeleev's periodic table has following defects.
i) Mendeleev's periodic table gives no idea about position of isotope:
ii) Ifelements are arranged according to increasing atofpic mass then.
masses, Potassivim (K™) should place bef Be sonar")
Nickel (Ni**) should place before col alt(co™)
But, Se
Argon (Av “) is present before Potassium.
reach cjg) Cobolt (Co™) is present before Nickel.
iii) Mendeleev arranged alkali metals (hijNa, k) ete with coinage metals (Cu, Ag,
Au) etc but there is a large differance ‘between their properties.
iv) Lanthanides and Actiqides have been arranged in periodic table which is
against periodic Law. +
v) The difference of atomigi plaerer between two successive elements is not
constant therefore it is difficult fo determine missing elements.
vi) This table gives no,jdea about structure of atom.
MODERN. PERIODIC TABLE OR MODERN PERIODIC LAW:
Ya,
is disca TRODUGI TION:
\Theimodern periodic law was proposed by Moseley according to
ncreasing atomic numbers.
7 3TATEMENT:
ddan je stated that:
SIXTH P
Rubidium Rb f i
Cesium @ cs o)
Francium rr } HD
v) They all are metals, (except hydrogen) p
vi) They are highly reactive and usually form jonic bonds. iv)
GROUP ILA: = y Q
i) This group is hen ‘as “Alkaline Earth metal”. BEVENT
ji), Thélr valency 1s “+2” 7
iti) * ThBy,flave two electrons in their outer most orbit. i)
iv) | The.eléments of this group are: Ca +2 Mg") a }
\
t “e
i PERIODS; :
‘There are seven periods in the modern periodic table. The salient My)
features,6f periods are as under.
FIRST PERIOD;
DEFINI
i) It certain two
ii) _ Itis the shortest period in the pe!
iii) This.period correspond to the k-shel
‘elements Hydrogen (H) and Helium (He)
riodic table. i
11 or first orbit. p called
tomic r
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IX Chemistry
Chem
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SECOND AND THIRD PERIOD;
i) * Second and third period are called short periods.
ii) Each periods carries eight elements
iii) Second period starts from Lithium and end at Neon, Elements of seco,
period have two total no. of orbit.
a iv) Third Period starts from sodium and end at Argon
. have three total no. of orbit.
°° ®t OURTH AND FIFTH PERIOD;
i) Fourth and fifth period are called Long Period.
i) Each period carries eighteen elements.
dashes) ili) Fourth period starts from “K" and end at =
have four no. of orbit
iv) Fifth period starts from “Rb” and eqd at “
five total no of orbit.
lements'6f third period
s
‘lements of fourth period
v) _ Ineach period, eight elements are norntal while ten elements are transition
elements.
\
SIXTH PERIOD; ¢
) Sixth period is referred to.a3 longestperiod.
ii) This period consist of 32 ele nth
iii) Sixth period starts from ‘Cs' and end at ‘Ro’. Element of sixth period have
six no of orbit.” © Bs
iv) _ In this period, eight glemegtsjare normal, 10 outer transition element and
14 inner transition element known as Lanthanides or race earth metal.
SEVENTH PERIOD; a
i) Seventh period referred to as in.complete period.
ii) This period starts from ‘Fs’. Elements of seven period have seven total no
) of orbit on
7) i Uptill now cight normal elements, 10 outer transition elements and 14 inner
transition elements known as Actinides.
iv) “Tae element with atomic numbers 109 and 110 has also been discovered.
he salient
ATOMIC RADIUS;
DEFINITION; 5
The distance between the nucleus and the extent of electrons in orbit
3 called atomic radius. OR
Half of the distance between the nuclei of two similar atoms is called
tomic radius of both the atoms.@ A
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It ts measured In Angstrom unle(1A’ = go TREND |
FACTORS ON WHICH ATOMIC RADIUS. DEPENDS: ss increase i
S ratomferachaa depence uponevo ¢ ri a
)) Number of shells ~— f
ii) Nuclear charge 2 yo
Y TREND |
TREND IN PERIOD; ih fd
\s decreases b
From left to right in a period the atomienad Cause Jocroase
1g in same orbit.
number of electrons are increasin:
[ Eleven [ Na | Mg
torical a =e i
ears tal Sto ea
TREND IN GROUP; ¢ Se
From top to bottom in graup, thewitomic radium increases becauseEFINIT
number of electrons are increasing with increase a neal of orbit. Pe
rer ectrons
Jotential
INIT;
sere
a é =x!
© pL ECTRONEGATIVITY: 2XPLAI
DEFINITION:
i Thélfndéncy of an atom in a molecule to attract shared pair of
ey }
electro totseregs called electronegativity:
FACTORS. ONWHICH ELECTRONEGA TIVITY DEPENDS;
“lectronegativity depends upon the following factors. i
) mic size
ii) Atomic number i
jij) ~ Electron Affinity i ‘
iv) Jonization potential energy
*ERIO.
CHARACTERISTICS; ‘BRIO.
negativity than any other group in periodic croasc
Jue i.e. 4 which is stander
iROUI
* Group VII-A are more electro!
+ Fluorine posses the highest electron
¢ Elements with high LE and large E.A
jegative val
have high E.N value
Icrease
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IX Chemistry
TREND IN PERIOD;
From left to right in a period, electronegativity increases because of
increase in force of attraction of nucleus.
Oxygen = 3.5 ;
a Nitrogen = 3.0 y
Carbon = 2.5
TREND IN GROUP;
From Top to bottom in a group, “ye +4 0 ae of
b
'eCAUse Jecrease in force of attraction of nucleus.
ELEMENT
Fx
ch
Br
i
IONIZATIONPO? ENTIAL;
s becauseJEFINITION: is
“The amount of energycequiret z release the most loosely bonded
Hectrons from the outer most orbit c ag. atom (in gaseous state) is called ionization
rotential (Ionization energy)it
®, \
5 Ais
leis measured in kiJo Joule/mole or electron volt (e¥) per atom.
JNIT;
LLLiitt
EXPLANATION; 3
1312 kJ/mole,énergy is required to remove an electron from an atom.
[pair of go WM+e H = 1312 kJ/mole
‘ % Similadly lonization energy of sodium is
{ Nat. Nate H = 495 kJ/mole
\_ The Teaction is endothermic in nature due to absorption of energy
JACTORS ON WHICH I.P DEPENDS;
{The ionization energy depends upon two factors.
) 6 {Nuclear Charge
ii) ~ Atomic Size
2ERIOD TREND;
Ionization energy increases from left to right in a period because
in periodic tycrease the nuclear charge and decrease in atomic size.
h is standan,
ROUP TREN. .
Ionization energy decrease from top to bottom in a group because
jcrease in atomic size.
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1X Che,
ELECTRON AFFINITY;
’
DEFINITION: Re
The amount of energy releases during addition ef an electron f
Affinity”
outermost orbit of an atom is called Electron
RB EFINITIC
UINT;
Itis measured in KJ/Mol or e.v per ator”
: toms toge
CHARACTERISTICS: fe ie a
7) Electron affini’y for the addition of first clectronjsinegative i.e.lenergy j,
released. N |
sriem ool TATEM
i) Butfor further addition of electron it is positive pecdyse energy has to _—_,
‘between negative ion and electron.
1 their ou
added to overvome repulsion
Ore —* 0
O-+e—* oO”
VITYSDEPENDS:
FACTORS ON WHICH ELECTRON ARFINITYDEP. —
Electron Affinity dependsupon
:
EA =-1242 Ks/mol (EX. o,stiermie)
EA = +7810 KuJ/mol (Endo thermic)
two factors.
)) Atomic size ster mos
ii) Nuclear Charge
s
& *
veriodié table, E.A decreases because the addition
GROUP TREND;
Down a group in
new shell decreases its forcé
attraction.
EA in KJ/mol
ae EFINIT.
ES
324
z wan 295 je to tra
avi _ Mg"? + 07 f AELTING
figh
SOLUBII
Summary of Reaction: } FOL UB IL
Mgit# 07 22s pte
COVALENT B ood eon
DEFINITION: e ; --
1. The force of attraction between two.OrT re atoms which is produg,
due to'sharing of electrons is called oa gen I ohne
EXPLANATION: is Single
aa ef Double
4. Formation of Hydrogeh Molecule: ; Tripple
a The electronic confugration, of hydrogen atom IS given below: °
H: (At. No. 1): K fis i
ii) Two hydrogen atomsycome closer to each other and share their electra,
Hence a covalent bobd is produced between hydrogen atoms,
Hex HorHe
2efinitic
Hit x H
2. steeiiced ecw,
* Thaformation of covalent bond between one carbon and four hydregey) sharin
atomto produée methane may be given-as:
‘xampl
\ av)
> Hx xHorCHs
definiti
> sharir
xamp
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1X Chemistry
DIFFERENCE BETWEEN IONIC BOND AND COVALENT
BOND
en A IONIC COMPOUND | COVALENT COMPOUND i
(B srate:
They are hard crystalline solids | They are found in the for
‘2 | (amorphous) liquid or gas)
AELTING AND BOILING PoInT: _|
figh Low (i.e. why calfed volatl
SOLUBILITY: \ |
soluble in water | nsotube iv \
2ONDUCTION POWER: (pou \
500d conductor of heat and electricity \ Bad Lane off.eat and electricity
‘.
@ ee etal Saw
is Produc, TYPES OF COVALANT BOND:
According to No. of bonds.
Single covalent bond
Double covalent bond
Tripple covalent bond te F
* According to polarization
+ Non-polar covalent bond
cir lect, + Polar covalent bond
:.
SINGLE COVALENT BOND:
2 lao oe
Itis a'type of covalent bond which is produced between two atoms due
r hydrogen? sharing of single pair of electron.
efinition:
‘xample: «a
AL CL Clor Ch,
H- Cl or HCl
H-N-HorNH3
|
oo :
DOUBLE COVALENT BOND:
Yefinitio
It is a type of covalent bond which is produced between two atoms due
> sharing of two pairs of electrons.
ixample:
O=O0o0rQ,
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TRIPLE COVALENT BOND: PEFINITI
Definition: “ teh
It is a type of covalent bond which is eravend bi woolen Baiccie te
to sharing of three pairs of electrons.
? } DEFINITI
Example:
~d
or Nz
= H C2H2 (Ethane)
H-c
ls
COVALENT BOND:
cs
NON-POLAR C'
ts
DEFINITION: ‘ ,
It is a type of covalent bond which iepPoauel d between two simy il) 4
‘atoms having no difference between their lectronegativities. wm
y
EXAMPLE: a) wie’)
Hz, Cl, O2, N2 ete. \ as
LENT BOND: pone
POLAR COVA!
DEFINITION: ®.,
Itis a type of covalent bond which is produced between two dissin
atoms having a small difference of electronegativities between them (differeng,
be less than 2)
HGla, NH;,*Water (H20), HF f y
; \®*
wa DIPOL
oeenlcit» an
% fecule having partially positive and negative charge atoms :
dipole. ; 5
Pe miticr: ,
Chlorine js more electronegative than hydrogen therefore jt 7
itself. HAPE
partially attracts shared pair of electrons towards
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IX Chemistry
DIPOLE - DIPOLE INTERACTION:
EFINITION:
The fore af atracton beeen 9 apes nolcule having pg se
Ind -ve charges) produced due to their partial +ve and -ve nature is called dip.
>
i. CO-ORDINATE COVALENT BON Ae
ys 2EFINITION: ~ f Ny
} The force of attraction between two or more atoms whigh,is produced
Jue to sharing of electrons but electrons for sharing are provided By 9 simple atom.
:XPLANATION: he
two sim, i) Atom which accepts electrons is called acceptor,
iii) Co-ordinate covalent bond is representedjby and arrow whose head
represent the direction of donation of electron
iv) Both the ordinary and co-ordinate covalent bond containing compounds
eh
have similar properties. {
s ve
‘XAMPLE: hg
i) Atom which provides both electrons for sharing x Donor.
1) mI 4
1 £0 dissin
| (differency
HAPE OF METHANI
je atoms is) © hemical formula: CHs
+. Structural formula: H~C-H
. Dot and cross model: Hx.C.XH
+ Lewis model: H- C-H
therefore it” Plape
HAPE OF AMMONIA:
* Chemical formula: NH3
. Structural formula: H—N—H
. Dot and cross model: H x .Nx.H »
+ Lewis model: H~N-H
+ Shape.
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SHAPE OF WATER:
. Chemical formula: H20 *
. Structural formula: o-H .
thapter
Dot and cross model: :0 x H
Lewis model: :O-H
. ‘Shape
bs
HYDROGEN
*
DEFINITION: “od }
“The force of attraction which is present tween electropositive
hydrogen atom and neighbouring electro negative atom fegcienconeica atom,
neighbouring molecule) is known as “HYDROGEN BOND” » Solid”
ap
EXPLANATION: ‘ JQUID:
Consider a molecule of HF. In, HP hydrogen has a partial positive ¢
Vine. Fluorine has a partial regaled liq
due to less electro negativity as compare te fuer
charge. s ¢ e ‘, SAS:
The partial positive hydrogen atom starts attraction the neighborin
luorine atom. This force of attraction between two molecules 4.1.4
s
partial negative fi
partial is known as “HYDROGEN BOND”
EFFECTS OF HYDROGEN.BOND:
ting and boiling point.
i) Hydrogen bond incr yses the mel
ji) _ Due to presencesof hydrogen bonding some covalent compounds hagarticle
and volatile Jiquid state. bey pos
liquid state inStead/of gaseous
2OMMC
a ' ranger
» \o@ METALLIC BOND: ee
OLID
ich is developed between the atoms or}
ud is known as “METALLIC BOND”, »,
nother
psition
perinir 10)
e\force of attraction wh!
to presence of electronic clo!
a metal
1QUIL
heir p
ave ar
yan in
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IX Chemistry
.
hapter # 06 STATES OR MATTER:
AATTER.
penk
Ss
“Matter is any thing that ‘yas mass & occupied space”
“ 7
MMON STATES OF MATTER: N
There are three common states of matter i.e me Liguid, aid Gas.
positive SOLID: d ?
tive atom, “The type of matter that has definite shape, & definite volume is call
Solid” e
IQuiD: ‘epee
positive g “The type of matter that has definite yalumedbut no definite shape is
rartia| negel!@4 tui \
anton tA! _
n ie
a borin, “The type of matter that has neither definite shape no definite volume is
cules dajjed as gas” \»
KINETIC MOLECULAR THEORY:
IMON FEATURES OF SOLID, LIQUID, GAS:
According to kinetic molecular theory matter is composed of very tiny
pounds hayarticles, which are called as molecules. These molecules are always in motion and
rey possess kinetic energy. The three states of matter depend upon the
rrangements, motions and force of attraction between these particles. The
ifference between solid, liquid & gas is explained as follows.
OLID STATE:
je atome ory In solid state the molecules or particles are tightly packed with one
5 BOND” ther and tliey have only back & forth motion (Vibrational notion) about their fixed
ositions. %
IQUID STATE:
In liquid state the molecules are not tightly packed with one another.
heir position are not fixed & they can move in all directions. Hence Liquid does not
ave any definite shape. But in liquid state, the kinetic energy of molecules is less
jan in the gaseous state.
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GASEOUS STATE:
ee rc aseod away from one another an,
In gaseous state
move in all directions easily. The cones!
are free to move about in all directions.
FuSIO! Cie
: if particles in
When a solid is heated, the Kinetic enera) o setbnslt
cas i Saprssed SG al
sntinued upto ce! H
forces holding particles of solig jp /-FUSIC
e Fi ae
Sy FFUSI
molecules are lying
in gas are negligible ana jg MEF
ive forces i
becomes hot. If heating is co
becomes enough to overcome the attractiv
fixed position & it starts melting.
MELTING OINT:
f
fusion of
molar m
‘is called melting pg,ample, H
Definition:
“The temperature at which solid Yortsyenel ti
nditions.
Explanation:
their fixed positions as well as their arrangemy- USC
ia, At mieltinig point the temperature Of Solid & jj
Inrough heat. It means in this condition ye Ole
Siquid m
drtate from solid to liquid & this change,
Imi of w.
At this point solid particles lose
thus solid is converted into liqui
remains same until all solid is melte
rise in temperature is used in chang
called fusion. Ss. 5
% )} whole v
EVAPORATION: a!
the Kinetic energy of liquid molecules increay
When liquid is heated,
Due to the increase of kinetic nergy certain molecules start escaping from the [RODU
les is called Evaporation”
surface of liquid and thisescape of molecu!
y 7, durit
es Ya, BOILING POINT: ENT
h vapour pressure of @ liquid becomes
‘4618 the temperature at whic!
equal to) eee applied on liquid. bunt
is
Boiling: >LaNy
is the process in which the Iiquid changes to gas at its boiling poi,
VAPOURIZATION: sy
At boiling point the temperature of the liquid remains same until ag
AMPLI
the liquid is evaporated or vaporized through heat.
‘The rise in temperature is used the change of state from liquid to ga
vendec
this change is known as vaporization’
ugh pa
powe:
fom zig
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1X Chemistry
er an 2
and ght/EFUSION: ,
The spreading of a substance through a medium like air or liquids
Wied diffusion.
i The rate of diffusion of a substance depends upafits molag maegler\y
Ses gpnsity. } e
é nei
7) : wad
fsolg wHEEUSION OF GASES, ~d AS
A Scottish chemist, Thomas Graham in 1846 studied the Fate of
fusion of different gases & formulated Graham's law. This law states that,
‘The rate of diffusion of gas is inversely'proportional to square root of
molar mass or density. *
In other words,
ighter gas diffuses much faster than heavier one. For
elting pjzmele, Hydrogen gas diffuses four timcs faster than oxygen gas at similar
inditions
rrangeme£EUSION OF LIQUIDS: i
sora i Liquid is intermediate between gaseous & solid states. Like gases,
dition thlid Molecules are able to move and.thus flow and diffuse. The rate of movement
is change {1/4 molecules is smaller than gases. For Example; 2 or 3 drops of blue ink in
im! of water in beaker. It is seen that blué colour of ink spreads slowly in water &
whole water becomes bluish after some time.
| BROWNIAN MOVEMENT:
| from the RODUCTION: {
This property first of all observed by British Botanist, Robert Brown in
7, during the movement of pollen grains in water by microscope.
FINITIONS “ele
‘
“A Continuous, rapid, zig-zag motion of suspended particle through the
tium is called Brownian motion’
1 becomes,
boiling poin Ifa drop of liquid with particles suspended in it, is observed under a
roscope, it is seen that particles are not at rest but they are moving in all
A s - ee ps
me ctigns in zig-zag motion. This motion is called as Brownian movement.
me until alle
AMPL.
| liquid to ga Mix some powdered sulphur in water and stir it, after stirring filter the
2ended sulphur some of the sulphur particles are very small & they can pass
ugh pares of filter it. Now put a drop of this filtrate on slide and examine it under
powered’microscope. It is observed that sulphur particles perform rapid
Jom zig-zag motion through the medium & this motion is called Brownian motion.
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IX Che,
, Chapt
GRAHAM'S LAW OF DIFFUSION: ae
GRAHAM’ 3
STATEMENT: In 1
Tie rate of aifrusion of a gas fs Inversely proporignal £0 the fee hydro
ofits molar mass or density. iy
By ow
MATHEMATICAL REPRESENTATION: a
Rate of diffusion « _1_——— s HW
Moh Mass or Density aa
In other words, lighter gas can diffuse fastegznan hea ercases ae
jumber is
Exampl
vedio than dkygen 92s at simigCCURE
Hydrogen gas diffuses four times
Itis
conditions.
composes
Abc
et wi puna
s 1.11% hy
ompoun
a a DUST.
See “oke St
Su Mie Wh
ie afte Syster
jquatio
X 20 C
; ‘ydroce
fi aah Genleved A- 1Gr ad’
,
quatior
4. By Electrolysis of Watefey * |
When electricity is passed through water containing few drops of acido, —2N.
J
Hz and O2are liberate.
Equation: if ca
2H:0 Electribity 2H: + O2
Reid jBase : With |
Po! a
PHYSICAL P. OPERTIES OF HYDROGEN: rmed. {
‘All those properties of a substance that can be identify by over five sen
skampl
called physical properties. : Chem Webware meritorious.com pk
IX Chemistry
1d reacysHAMICAL PROPERTIES OF HYDROGEN:
Following are some important chemical properties of hydrogen.
Detomposition of Hydrogen Molecule:
b When 104 Kcal are supplied to a molecule of hydrogen 1000 k, decompos:
to atomic hydrogen.
H; 100k _, H+H AH = 194 Keal/mol
reir oxygen. “
in y Ne
#500'c ,. Reducing Agent: a
}40d ea, When hydrogen reacts with metallic oxide it reduced the oxides by removing
e ely:
rs
‘quation:
Cuo +H Cu +H,0
Hydrogenation:
The addition of H2 to other compounds Is called hydrogenation.
lack ang quation:
CO+2H: 2moz CH; ~ OH ‘ ‘
ns yi
409°C (Methyl Alcohcl)
te FP
When hydrogen reacts with metal metallic oxide hydrides are formed.
quation: wy
sofacidg, | 2Na+H;———-—*2NaH!* ;
(Sodium hydride)
Cat+tH: ———* Caley
(Calcium hydrides)
With Non* Metals:
When hydrogen reacts with non ~ metals, non metallic oxide,hydrides a8
rmed.
+ five senseample?
2H2+Q2 —Igniton 2H,0
2N+ 3H, Fe,0) | 2NHs
500°C
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1 Chem,
USES OF HYDROGEN:
rant uses of hydrogen
Jeutitiun
Following are some impo!
wa
ii ttis used to purity metals.
jy) Itis used in making hydrogen fore “ i. itha
; ‘eh Bill) Itis
iv) It's s
v) Itis used in weather Balloons.
NASCENT HY!
‘during chemical reaction
DROGEN: we
ig in atomié form is ¢,
al
The hydrogen produced
Nascent hydrogen. me a i
Example: 5 ‘
Zn + 2HC] ——> ZnClz + 2H]
(Nascent hydrogen).
REACTIVITY OF NASCENT HYDROGEN: }
‘As the atomic (Nascent) hydrogen is highly. séacted so it immediately fo RITIUM
‘ded it is produce during the m — Itis
i) It's
hydrogen molecules therefore whenever itis nee
ii) Ith
reaction. ‘
Example: a iii) Itis
FeCl; + [H] zicl FeCl + HC! iv) It’s
(Nascent Hydroge?) (Ferrous Chloride)
Y ISOTOPES:
having same charge number but
‘of hydrogen are example of it.
All the elements: pifersn’ mass nina
called Isotopes. Isotopes j
ISOTOPES‘OE HYDROGE!
Itis ofdit hydrogen and have following features.
i) Its at jumber is 1 and mass number is also 7
ji) Ithas 1 proton in the nucleus and 1 electron in the orbit.
iii) It is Stable hydrogen.
. lissolve
iv) It's structure is as follows. .
otain fr
rough
ti
n Boi
Ww
spands
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IX Chemistry
Deutitium:
It is a heavy hydrogen and have following features.
i) It's mass number is 1 and charge number is 2.
; i) Ithas 1 proton and I neutron in the nucleus and 4 electron in the orbit
LB ii) Itis also a stable hydrogen , y
iy) It's structure can be shown as follows. 5
. 5
rm is cam s
li
*
9
‘ately fog FM P
ml yg It is radio active hydrogen and has fol!owing features.
ing the It’s charge number is 1 and mass number is 3
ii) It has 1 proton and 2 neutrons in the nucleus and 1 electron in the orbit.
iii) Itis unstable hydrogen. ;
iv) It's structure can be shown as follows.
's number a i (
; WATER:
JTRODUCTION:
eet i
Water igmost abundant compound in nature and is a universal solvent as well
jissolves almost every substance) therefore, it do not exist impure form. The water
stain from natural sources is called natural sources water and the water obtained
rough'some treatnicnt is called “treated water”. Distilled water is purest water.
n Boiling: ntoot
When water is boiled from O%- 4°C it contacts and from 4°C - 100°C it
spands.
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ulshan C
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se mareasmereessoweeorn en
On Freezing:
tract and fro “ith
When water is freezed from 100°C — #¢ itcont m.4°C~ oF we carb
expands. 7
Conclusion: fquation:
‘Aa the behaviour of water on boiling ‘and freezing is ape therefore c+H
vith Silic
conclude that water has anofhalous behaviour ?
Whei
2
PHYSICAL PERTIES OF WATER: a
SOF WA cal properties fate ® sie
Following are some i
i) The density of ws or at °C is one gm/ent } Vith Quic
ii) It’s freezing point is oC. Whe
Jil) It’s boiling point is 100°C ; ‘\
iv) It is universal solvent. i } quation
\ a0
CHEMICAL PROPERTIES OF WATER: i
Following are some important chemical pike ties of water. Jtrous C
With Metals. A ~~ Whe
Water reacts with metals in following to WAYS: N20
With More Electropositive Metals: ? (ATER |
up 1A and I! A it will from the yay Due
) ied
When water reacts with element of gro!
of these metals. e
) ii) Itis
a ry fii) Mar
‘2Na + 2H;O ————f 2NaOH +H:
Ca+2H,0 ——yrCa (OH)2+ He
e Int
sbstanc
With Less Electropositive Elements:
en, ‘réact with group Ill A elements. ystalliz
xampl
MgO + Hs D
Dest
cakes it
jetal: 4
has three different reaction with non - metal.
With Chlorine:
When water reacts with chlorine it forms HCI.
Example: es
Ch+Hz0 —————+_ HCI + HClO a
GIO HCI + [0]
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IX Chemistry
vith Carbon,
Ch When carbon .eacts with water it form water gas
’
quation:
{ C= HO
efore .
With Silicon
fs: ae
co+Ms
When water reacts with silicon it form it oxide,
Si*H:0 + SIO+H,
ee
) 4 \
Yith Quick Lime:
When quick lime reacts with water forms shacked |j
quation:
CaO +H; —+ ca(oH: 2
itrous Oxide. Ks
When nitrous oxide reacts with water it dissol¥gs it ‘0 from neutral solution:
N,O + H,0 * Neutral He (
/ATER AS A UNIVERSAL SOLVENT: oa
mm the iy Due to following features is Known agyuniversal solvent.
e
Yi i) it dissolves majority of ionic compound and the covalent compound.
ii) Itis electric in natureland a polar.
iii) Many of the gases like Ammonia, Carbondiovide etc are soluble in water.
ry
WATER OF CRYSTALLIZATION:
In molecules of water trapped in between the crystals of the crystalline
sbstances during the evaporation o/ the saturated solution is called the water of
ystallization.
xample:
During the evaporation of separated solution of copper sulphate five
olecules of Water are trapped between the crystals of copper sulphate which
fakes it colour blue.
juation:
CUSO,+5H,0 —~—~—~—«CuSo4 5H20
(Blue Colour)
On further heating we will get anhydrous white colour copper sulphate.
CuSO, . 5H20 CuSO, + 5H20
* (white Colour)
to Mat
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soFT WATER:
wore dissolves carbonate, b
Se nionee hoon ood Ea
ater is the universal solvent tr
As wi
chloride, sulphate of calcium and magnesiv®
Definition: >
whieh produces more lather soap S05! called soft water, gi lon Exc
» This
HARD WATER: f scence of
ation:
is called hard water.
CAUSES OF HARDNESS.
MgCl
“As water dissolves many substances Ih? carbbndioxide and atmospyy
calcium, magnesium on following through their beds and'produces carbonay) By Usi
ates of calcium and magnesium Whig” produces Hardness in water. or
yich is in
bicarb
TYPES OF HARDNESS:
There are two types of hardness . qation
)) Temporary Hardness ii) pérmarient#Hardness Mg
i), Temporary Hardness By Usit
The hardness in water due to Bres db of bicarbonate of Ca.and Mgigg in th
Temporary hardness e ches all
uation
ii) Permanent Hardness: * ),
The hardness in water dllle to presence of chloride and sulphabof calcjy 9S
Ca.
Magnesium is'permanent hardfess.
OPER
2
METHOD'S OF REMOVING HARDNESS:
gihardness which areas follows; j) It’
is of removin:
These are two
; Ore or By rps
i. By Heating: 7 p i
Témpo. rdness can be removed by boiling water as it contains, ss
Bicarbohate 8fCaand Mg which changes into carbonate of Ca and Mg are ing) a
vi) It J
vil) Wei
(CO). ———*_ Cay + CO2* H20 DROS
(Insoluble) | af
ii) Clark's Method: damn
ition Ic
Temporary hardness can be removed by clark’s method in which shacke,,
(Ca (OH)2) is dissolved in water which converts bicarbonates Ca and Mg intod
respective carbonates.
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IX Chemistry
te, by
eal Ca (HCO); * Ca(OH); + 20aC0, + 24,0
Mg (HCO); + Ca (OH): + MyCO; + Caco, + H,0
> m t
#) lon Exchange Method:
ator
This method is used to remove permanent hardness which is due to tt
esence of chloride and sulphate of Ca and Mg. In this method laws of Ca ahd,
le removed By using washing soda Zeolite and sodium whi ude
ation: 8
aS. + Nay * Caco, +
CaSO. + Naco CaCO; + Na:SO. i
(Insoluble)
MgCAs + Na +
a co. MgC; + 2NaCl }
carbonay) By Using Caustic Soda
in water, In this method caustic soda is added 4 Sc a hydroxide of Mig
sich is in soluble in water.
quation: » ~d
MgSO, + 2NaOH * Mg (OH)+ Na;30.
JA (wealuple)
By Using Zeolite: ¢
Ind Mg igg In this methed water is passed throUgh'fevsin of sodium Zeolite which
ches all Ca and Mg and.makes witagsotp
uation:
ahof calc, C#SO. + Sod. Zeolite WN \, Carzeolite + Na:SO.
Ca. Zeolite + NaCI Li -' Sod. Zeolite-+ CaCl;
OPERTIES OF HEAVY WATE!
ollows: {) It’s density is 1.19nven’.
ji) It’s malting point is 3.8/C
fil) It’s boiling pointis 101.4°C
v) It's Vapour presence is less than ordinary water.
{Mg areinsy) t's refrattive index is less than ordinary water.
Vi) Itis used as a tracer in biological method.
fii) Iti:used as Moderator in Nuclear friction reaction.
DROSCOPIC SUBSTANCE:
All substance that has tendency to absorb mixture when exposed to
Sees sPrere. These substance some times from their solution and some tirnes the
jtion loses it's concentration. All the substance are called hydroscopic
vhich shackstance,
ind Mg into tt
‘ontains
Mc
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i: meritorious. gursy
SS a 3 Near KMC PS
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wtjain Can
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INTRODUCTION: st _
Sir ic thie i tial compound forte every living thing neeg hapter |
Dee ee bce ,d of water. Water available is used in ver) ved
1% body is composed © : ; it v
an
purpost
of vital significanc'
water is con:
impurities like sewage wate
polluted.
ixture wi
ormatio
The
jal m
domestic, ag
es { oq WrBoDu
POLLUTED WATER! ES fle, can
itis contaminated b of per
dered to be poluted when I contaminated by Sever,
i! 1, industrial water agriculture pesticides Pei curren
J py mancourren
ea f4 Cart
: ER POLLUTA: amond,
CLASSIFICATION OF WAT ; TANTS:
i) Oxygen = Demandin: Waste: }
ic sewage, indus’ triakwaste; slaughter houses ang
ieauses danger for human
2 ‘tateri
‘At includes domesti
¢ substances contamina!
al calle¢
pulp all thes‘
athracite
aquatic animals. y
ii) Synthetic Organic Gompound:,§ & a B ‘
These includes all man made chemical like pesticides, insecticides, 14 Cart
detergents, paints, fibers, plastic etc ‘makejwater polluted and harmful for ee
well.
ing Waste.
iii) Diseasing Causi > \
When micro-organisms through ‘sewage and industrial waste dissolve,
usffor life and cause diseases: j
water become very dangero!
iv) Agriculture Water flution:
‘As to enhance ena yields farmer are using fertilizers, pesticides gfferen
Spmakes polluted and dangerous for life. or
organicywaste whic!
wy
Cryste
QUALITY. OP DRINKING WATER:
funicipalwater is used for ‘domestic and drinking purpose. This was, af
ss ! 4
led protable water.
Amor
Portablets Properties: a)
7e important characteristic for protable water as follows. , °)
i) It should be colourless, odorless and tasteless. ° Ca
it should be free from all kinds of pollutants. tel
iii) It's PH ranges from 7 to 8.5. fice
at
iv) It's hardness should not be above than 150.
v) It should not stain clothes.
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IX Chemistry
M4 CARBON:
a Carbon is the 16 abundant element in the earth’s crust and belongs Up
yf A ot periodic table and has 4 electrons in its outermost sil. \%
ral
= tem courrence: j s
Fie Carbon exists in free and combined state in natilresdA pure Tron Itioccurs as
Tg, Zo Grephite and Buckrnster.n combined state, ifexet oe and its
= ES: ixture with hydrogen, oxygen, nitrogen, sulphur etc. J
Ney
>rmation of Coal: <
: ‘
The first stage in the formation of coal is peat. It is soft, brown, spongy
or hi . 7
“man waterial made by partial decomposition of plants. Peat thafh converts into brown
al called lignite, than a soft coal called Bitumenjand finally into hard coal called
athracite.
uses ang,
‘
a 1e Carbon Contents and Energy Values
mful for hy = os i 2
. FUEL CARBON CONTENT | ENERGY VALUES |
wa [5% rw 19800 KJ/Kq
= See DL 18700 KJ/Kg _ \
te dissolve, ‘Lignite | % 61, |__ 20900 - 25700 KJ/Kg
|__ Bitumen | | 32100 KJ/Kg \
_ Anthracte er ea Tse 32600 KJ/Kg |
pesticides afferent Form of Carbon?
In Free State, carbon occurs as following forms;
Crystalline Form:
e. This way 2) Diamond, b)Graphite c) Bucky Ball
Amorphous Form:
‘ a) Lamp Black b) Wood Charcoal c)Coal d) Animal Charcoal
e) Gas Carbon
* Carbon exist as carbon Black, it is produced when metiane is heated at high
temperature. -
* Coke is a pure form of carbon obtained when coal is heated strongly in
absence of air.
+ In combined form, it exists as natural gas and petroleum.
+ Carbon also exists in the form of CO and CO; in the atmosphere.
+ Carbon also exists in the form of CaCO; which occurs as marble.
VS.
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IX Cha,
esi Pine
Main Campus:
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Allotropy:
rms of the same element in
the, J
“the existence of two or more different fo
Thes
state is called allotropy.
h are as follows;
Allotropic Forms of Carbon: :
forms of carbon whic
There are three allotropic
i) Diamond: 2 i
itis the crystalline form of carbon and is found in South Afric }
: i
o6
Brazil and India.
Properties:
7) Itis the hardest natural substance.
gm/em’.
ii) Its density is 3.51
jij) Itis a bad conductor of electricity. C
iv) Its melting point is 3500°C. _
v) Its refractive index is 2.54
ii) Graphite: g % Final
Jt occurs as plumb ago solid and found mS iberia, Canada and Srilanka, rystal late
Properties: os! Bale)
j) Itis a dark grey crystalline solid. itera
i) It is a soft and greasy — [a
iii) its density is 2.2 gms/Gm’. Le iia g
iv) Its melting point is 300°C. _ oo.
v) It is a good conductor felectricity.
In 1985, a angfleghery made by two English scientists who vapour,
graphite and got game Ergnts of Cw and found thet lt fs.2 different form of Gay
which seems,exactly likéia ball therefore they named it bucky ball. This is the fg,
Carbon soluble iorganic compounds.
Structure df,Diamond:
Theicrystal of diamond is octahedral in shape but the basic crystal is
tetrahedral ih shape in which C-atoms are co-valently bonded as shown below, a
tale
las wi
a distar
ucture
vee of t
nducto
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IX Chemistry
tin the, J
These basic tetrahedral units together will form an indefinite giant as shown
pelowe)
Finally this brings strength and uniformly bonded atoms to form a hardest
Srilanka, rystal later. The bond length between two C-atoms ig 1-54 A° and bond energy is
47 KJ/mol. \
tructure of Graphite:
In graphite the C-atoms from aflat basi ic hexagonal ring. It can be viewed as a
.._ 40 dimensional layer lattice as shown below;
© vapour }
ym of Car, P
is is the fq
stal is
wn below.
Inigraphite the C-C bond length is 1.42A°. They have strong covalent bonds as
sil as which are responsible for high melting point. The two successive layers are
a distance of 3.35A°. The inter layer bonding is very low therefore it is soft. The
ucture of graphite is more open therefore it is less denser. Unlike diamond only
‘ee of the valence electrons out of four are in bonding therefore it is a good
nductor of electricity.
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sotropes of Carbon. By X-ray oreta
‘except coal which occurs
rs. 7j) Combin
red as follows; “Athi
Amorphous Forms of Carbon:
its al
The amorphous forms are not
like graphite
Observed that they all have structure
naturatly In urines. The other amorphous form C2” be prepa’
Ce al
i). Coa
Coal is originated by decomposition of plants and cers under sro 3 eam le:
they decompose in absence of air under pressure and CO2, Witer andp c+ ae cz
liberated laving behind material called Coal. ome
ii) Coke:
Coke can be obtained by destructive distillation ae In a we va ii) Reduc:
upto 1300°C in absence of air so that all the volatileimpubities are nhoved, Carb
In these volatile impurities coal tar and coke arevabtained in which coke, & Whe
used as a fuel. 2 os ee
iii) Charcoal: N. {i xample:
it can be obtained by heating wood, nut shells, Bones, sugar etc in very), Be
supply of air. ae
ae bt 2Pbi
Properties of Carbon: 2Cu
Physical Properties: ‘Ne, 1) React
i). Except diamond, all allotropes Srearbon are in Black or grayish colour, ee
ii) Carbon is odorless afd t tasteless. pip nurS
iii) Its melting point is very ‘high ie. 3000°C. Cr.
jv) Itis insoluble in commdnsolvent (water, acid, alcohol) cw
Chemical Properties: 4 ; | Cateni
Following are sofe important chemical properties of carbon. The
)p combustion polices
There are'two ‘Gombustion reactions of carbon; Laster
~ Bes of
dn Exedes of Al Fol
Wileg catéén is burned in excess supply of air COz and heat energy are 1h
produced. 4 i) 3
c+0 Excess co, + sHasesKiimol 4) &
aie iv) G
— vy) G
In Limited Supply of Air: vival
When carbon is burned in limited supply of air incomplete combustion ta Vi) Mt
and produced carbon monoxide (CO) vili) It
20 + Oz limited 2co bd 7G
Air : x) iG
xi) C
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aya IX Chemistry
curs) Combination Reaction:
ws}
Athigh temperature carbon combines with elements like hydrogen, sulphur,
Zalciim, aluminum forms their compounds.
rth Whexample:
c fC +22 High tomp CH. (methane) E
a +28 High temp CS2 (Carbon disulphide) a bd
\ Cis
Peay il Reducing Agent: 4
ve heat 4 “ 3
wved, | Carbon has great ability to react with 02, therefor® ¢arbon aets) 1STeducing
oh coke ent: When Carbon reacts with metallic oxides, 3
a
a ee a
§ mperature and convert them into free metals.
xample.
Fe;03 3-30 Sa
2zn0+¢ == —————>
LAIR I) Saez
LEO.
2Fe +3CO
2Zn + COz
2Pb + CO,”
2Cu + CO;
7) Reaction with Oxidizing Agents }
colotn When carbon reacts with strong oxidizing agent such as nitric acid and
ulphuric acid and gets oxidized to liberate CO.
C+ 4HNOs Hot. CO; + 4NO; + 2Hz0
(
C+2H2SO, ___Hot 5 CO2+ 280, + 2H,0
| Catenation: \_' aye j
The property of carbon/in which it has tendency of forming long chain and
ag-like structures, therefore it is known as catenation. _
ses of Carbon»,
Following are Some important uses of carbon;
i) Diamonds fare used as gems and precious stones.
nergy are ji) 'Black diamonds are used in drilling.
iii) Tiny particles of black diamonds are used for polishing tools.
iv) Graphite is used as lubricant.
v) Graphite is also used in making high-grade steel.
Visit is also used for making electrodes.
rbustion tal Vil). It is used in lead pencils.
vill) It is also used as neutron moderator.
ix) Coal and coke are used as a fuel.
x) Coke is also used in extraction of metals.
xi) Charcoal is used as domestic fuel.
/mol
to Matrio
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ae sip area
i atrone a
2
ey Uk Une a
Seis rtoroue ouch
com.pk
TX Chen,
decolorizing Sugar
xii) Animal charcoal is used for i
xiii) Carbon Black is used in mar
xiv) Itis also used Is making shoe PO
xv) Carbon fiber is used in making plas!
SILICON:
tic bags:
Introduction.
‘on lies between metals and Nomis,
metalloids. It belongs to Group IVA of the period
fica (SiO2)
carbon. In ancient time, it is known 2s sil
ic
Example
‘Sand. In 1823, Berzelius named it as amorph
Occurrence:
Taaeveeans thas sand,
cur in the form of silica SU@
Silicon acct
jartz and flint an‘
etc. Pure crystalline form is qu:
metals therefore, itis kndbedosy
ous solid “Silicon”
°
g rubber tyres
iter ink.
table and comes a
)
5
i
quartz, flint, kieselguhr, ,
ga palforms are kieselguh,
and agate. In combined from it occurs ‘as complex sil
_ > a
————— —__ fai
['S.vo| Name of Silicates | __ ~ Formula ih ne Uses |
1 Feldspar __| Kz0 ALsO3 6sio: j Ceramics, glass, pottery, abrag,
2. | Kaolin (China clay) | Alz0s Bio, 2Hio | _ eeicrosker
le Electrical insulator resistance,
3 Mica high temperature
(4 | Tale (Soapstone) 310 4Si02 HzO Ceramics)
Cal Asbestos Cad 3iigo 48/02 Heat insulation, fire proofing
Properties of Silicon:,
Physical Properties:
i) Itis brown Colour powder.
ii) Its specitf@gravity is 2.35.
‘stallinesSilicon is grey in
iv) Ithas Dea pion melting point i.e. 1410°C
v) Its Boint of boiling is 2600°C.
soluble in water.
ad conductor of electricity.
Chemi€al Properties:
Following are important chemics
i) Reaction with Alkali:
When Silicon is dissolved in hot Na
Hydrogen.
al properties
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olour having specific gravity 2.49.
of silicon;
OH it forms its silicates and liberate
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Rey 1X Chemistry
Equatio!
Na:CO; + SiO; H Naz SiO; +CO, +
(Sodium Silicate)
Now the Na,Si is dissolved in boiling water under high pressure to form a
viscous liquid water glass and it looks like ordinary glass.
Uses of NazSiO, (Water Glass): ‘Ne
i) Itis used for sizing of paper. s
ii) Itis used for fire proofing. .
ing chemical gi
iii) Itis used for making glue. Ne
iv) Its also used for preserving eggs.
V) The dilute solution of NaSiO3is used for maki
Chemical Garden: } he
selguhr, Make a dilute solution of water glass.(NazSiO.) in @ ass trough. Add ras
sala "8 crystals of coloured salts. Such as cobalt chloride, nickel stiiphate, copper sulphate,
‘guhr ferric chloride etc. Leave them for few days withoubtouUéhing the tough. You will find
your chemical garden grow with colourful plants of chemical. This is because of the
formation of insoluble metal silicates. ee
Cu* SO* sia) + Naz*’ Si? Oajaq) | CUSIO3 (5) + Naz Sa (acy
“(Blue ppt)
aa | © Silica Jel:
a When an acid is added in’ solution of water glass. It turns into a jelly like
© Proofing substance known as jel. Thejformula for this jel is SiOz nH20. On complete
dehydration of this get by heating, a had porous material is obtained known as Silica
Jel. gf i ;
Due to its large Tie area, silica jel is used as good absorbent. Itis oe to
absorb gases and'vapour Small bags of silica jel are kept in medicine packing
preventithe medicines. being spoiled by water vapours in the atmosphere. 2
i Is from industrial effluents and in the
Itlis alsO\used to recover valuable vapours from
reefing of petroleum.
‘,
\d liberate
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IX Chemistry
Equation: A
103 + He
m4 +2NaOH _ Hot »Naz SiO: Lanter
Combustion in Air: er >
When silicon is strongly heated in air silica |S produced.
Si+ Oz + SiO; silica Introducti
Preparation of Silica: y Nitro
po a8 manned it
Method 1. , family havi
When pure dry sand and Mg are heated in absence. or sitigo ie gormed. ee
S102 + Me heat _, Si+ 2MgO 3 2CCURR
nas ‘HCI so, that the unreacted Mg and Mgo Rave
Now the mixture is dissolved in dilute
ad settle down inthe container and remaining mass. In c
convert into MgCl which is insoluble
. .q S/O; the content is dissolveq
amorphous silicon is separated. To remove unreacte
in hydrogen fluoride as shown below;
—> Sif + 2H:0
Dalcium ar
natter suc
SiO; + 4HF — ,
‘ (silicon tetra fluoride) Preparatt
Method n \ From A
When the vapours of silicon chlor are passed over heated sodium or The
potassium, silicon is produced. , fF liquid ai
SiCi,+ 4Na Heat ‘Si + 4NaCl ‘ractioné
SiCh+4K _ Heat sit 4KCI Clee
Method 3: * } irther co
When the Silica (Si0,) i$ heated with coke in an electric furnace, crystals of pd then a
silicon are produced. : ver. Argc
ith boilin
SiO; + 2C. Heat Si+2CO
Electricfurnace crystals JAGRA\
Following are some important uses of Silicon; ;
i) Itis used in alloys of bronze and steel to increase their strength. 5
ii) Itis.used in making semi-conductors.
iii) Itis used as a lubricant. "
iv) Itis Used as a water repellent.
V) Itig\tsed in paints, varnish and polishes.
Sodium ate or Water Glass:
Water glass is prepared on strong heating of two parts of silica with one part
of sodium carbonate. It is obtained as a colourless glass with melting point 1090°C.
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On ~
a
IX Chemistry
Chapter #13 “NITROGEN AND OXYGEN”
P “= ROGEN'AND OXYGEN”
NITROGEN:
Introduction:
Nitrogen was discovered by Scottish Protanist, Daniel,
manned it Nitrogen. It belongs to group VA of the periodic t
‘amily having five electrons in valence shell.
DCCURRENCE:
Mgo Nitrogen occur in free state as Nz gas in air upto 78% by volumma and 75% by
aining ass. In combined state nitrogen occur in the earth crust as nitrates f sodium,
oIved 1
Zalcium and potassium as well as ammonium, salt. Nitrogen is also found in organic
patter such as Protein, Urea and Vitamin 8 Compound.
?reparation:
) From Ai :
The commercial method of producing nitrogen gas is the fractional distillation
f liquid air. In this process air liquefied and then fractionally distilled.
‘ractional Distillation of Liquid Air: 7
Clean air is compressed and then cooled by refrigeration of expansion it is
irther cools and liquefies. The liquid air is filtered to remove carbon dioxide solid
sof id then distilled. Nitrogen is the most\volatile with boiling point-496°C, distilled
ver. Argon which boils at4857°C and liquid oxygen, the least volatile component
ith boiling point-183°C collected at the bottom.
IAGRAMATIC REPRESENTATION:
11
e part
090°C,
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TX Chemigy
Ammonium Nitrate. Ammoniysnon-metals
‘ae with Sodium nitrate.
ji) Laboratory Preparation. 5
ined by heatin
In laboratory nitrogen is obtal
Nitrate is fucec ti onium Chloris <3
rate is produced by reacting Amm ac
Equation: i
NH,CI + NaNOz ——————* NH.HO2 + NaCl volume of a
NANO? __ heat___, Na+ 2H20 ? \ Liquetac
ary fe) Airis
Physical Properties: of 200atm a
i) Nitrogen is colourless, ordourless and tasteles7 92°) labial
ii) Pure nitrogen is slightly soluble in water. since
Fractio
iii) Itis slightly lighter than air. :
iv) Its boiling point is 196°C 2
v) Its melting point is 210°C
\ iqui
202. One d
£185 7°C
Chemical Properties: if x
Nitrogen directly combine with hydrogeM oxy: ahd magnesium to form indor a pre
their compounds. i
aborato:
i) With Hydrogen: he ci Oxy:
When nitrogen reacts with hydrogen, Ammonia is formed. srr
2kC
Equation:
N2+3H2 450°C 2NH3 ‘hysical
200-250 ator, i) Oxy
ii) With Oxygen: J Ones
‘Nitrogen combine with oxygen ‘at 2000°C to form nitric oxide. a i is
fas
Equation: $ v) It lic
3g + No—ced hot WgsN2- © nariiee
OXYGEN: With M
Introduction: intr! , Whi
Oxygen was discovered by Scheel in 1772 and Priestley in 1774 and Lavoisig,
named it oxygen. It is the most essential for all living thing. It belongs to VIA group quatior
of periodic table and first member of family having 6 electrons in valence shell. an
° i
Occufrence: id
arth, it occurs both in free and \ wie :
‘Oxygen is the most abundant element on e
Pombinedatate In jree state [tis presentas diatomic gas /n atmosphere alr Upto
21% by volume and 33% by mass. In combined form oxygen accounts 50% by massyuatio)
of earth crust. It constitutes about 88.8% by mass ofwater.Inmostabundant || s4
compound it is presentas silica, silicates, carbonates and oxides of both matals aac
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IX Chemistry
NOniyanon-metals to make up clays, rocks and sand.
{solation or Preparation of oxygen:
‘he oxygen is isolated by fractional distillation of air,
lume of air. The process includes the following two steps.
Liquefaction of Ai
Air is passed through caustic soda to remove CO: present in it. At a pI
of 200atm air id compressed, then cooled and allowed to expand rapid
jozz/e in a region at low pressure to cool further. The procegs is rep
igain due to which temperature reaches to 200°C and air.Jiquefie:
1s oxygen form 21% by
é
Eons
‘again and
tt
Ne
i) Fractional Distillation of Liquid Air:
Liquid air is led into fractionating tower through alfilter to weds traces of
302. One distillation Nitrogen is called at 196°C then in't
t 185 7°C and at last liquid oxygen is dried, compres:
middle Argon is collected
sed aid stored in steel cylinder
> form \nder a pressure about 100 atmosphere. }
aboratory Preparation: ‘eo
‘Oxygen can be prepared in laboratory by, ther
hlorate with little MnO; as catalyst. fal
2KCIO; ——+ 2KCI+302 w'
decomposition of potassium
‘hysical Properties: te, >
i) Oxygen is colourless, ordourless and tasteless gas.
ii) Itis neutral to moist litrius papers
iii) Itis slightly soluble in water
iv) Gaseous oxygen is about 1.1 times denser than air.
v) It liquefies at 183°C. |
hemical Properties:
With Metals: “~~
When oxygen reacts with metals, metallic oxides are formed.
oy | :
d Lavoisig, uation: 3
VIA groupl“ 2ca02 2¢a0
shell.
Lit 200;
With\Non-Metals:
ee and \ "When oxygen reacts with non-metals, their oxides are formed.
air upto
1% by massquatio: F
dant $+0, ——— So: 7
h metals am C+ 0; ———» CO
Matric)
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Wob.werw.meritor DE Chemig
i) With Other Compounds: compounds, forms meir respective Oxides Properties
hen oxygen reacts with other Se
Equation Equation
CH, + 202 CO; + 2H:0
2H.S + 302 © SOx+ 2H:0
4FeS +702 > Fe:0; +4502 2 2
eA
, Oxides: j an
ES merits excepéro:
Oxygen is very reactive and ‘combined with all 4 ee. c Pg joble gase, ‘4
‘and halogens and formed their binary compounds calle’ } ¥ yi
sao f 2 S
Classification of Oxides: we Peaster example:
‘On the basis of valency or oxidation state of OXY xides are classifiey, 4A! *
follows. 2Zn-
{ 5 > :
i) Normal Oxide: . Ne y a 2ropertie:
‘All the oxides in which valency Or oxidation)sta' slumber is-2 are normal vor
i
oxides. Normal oxides are classified as follows. ) Witte A
Whe
_/ Basic Oxide: baton
The oxides of metals are know#ilas basiioxides. iquation:
4 ALO
Example:: 2nQ
‘4Na +0; ———>_ 2Naz0
2Ca + 0, "20. ) Witte E
Whe
Properties of Basic Oxide: i ;
i) They are soluble in water and produce their hydroxides. quation
Equation: g Alz0
Naz0 + H20. -2NaOH cae
Ca + HO, Ca (OH)2 2 eutral C
ii) They aso reacts with acids to produced their salts aa
ion: 4
Equation: ». prvs i
MgO + 2He| —— MgClz + H20
CaO +2HNO3 ——+Ca (NOs)? + H20 xample
: Ww
a 2 ic Oxide: eroxide
The oxides of non-metals are called acidic oxides. All
yrmal ox
Example: é
S+0, cample
C+O,. Ns
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PP: Faraan Masjid, Karachi
1X Chemistry
properties of Acidic Oxides:
xides, They react with water to produce acids.
Equation: SO:+H,0—+ 4,50,
% €02+H,0-—+ H,c0,
They react with alkali to form salt and water.
ation: ~CO2*2Na0H __, Na,C0, +H,0
$03 + 2KOH_.,50,+H,0
Amphoteric Oxide:
The oxides of .\I2 Zn etc are called amphoteric oxi
sified a 4Al+302——* 2A1,0; ‘
2Zn + 02 ———» 2Zno “a
2roperties of Ampiroteric Cxide: i
i
Dr 5 i
mal witte Acid:
an, “a
When they react with acid salt and water is formed.
iquation: “_
Alz03 + 6HC| ————+ 2AIC1J# 3H20
2n 0 +H:SO, ——*_ZnS04+ H20)
OT
Witte Base: z
When they react with base|and water is formed.
Alz03 + 2NaOH ae 2NaAlOz+ HzO
Zn O + 2NaOH we Naz ZnO2+ H20
eutral Oxide:
All the oxides Which are neither acidic nor basic and are neutral to moist
mus paper are neutral oxide. ?
xample:
i) Water (H20) _ ii) Nitric oxide (NO)
iii) Carbon monoxide (CO)
2roxide:
All the oxides that contains higher proportion of oxygen as compared to
rmal oxides are called peroxide.
8804+ M202
Ises:
Industrial Preparation:
On large scale hydrogen peroxide is prepared PY oxidation of isopropyl} As Ant
alcohol. Bi
‘eaning v
Equation:
CH; CH 21H; + 02 Hz02 + CH - © - CHa As Ble
oH ° Hy
ol, feat
Physical Prope! aterials.
i) Itisjpale blue syrupy liquid.
ii) ‘eis soluble in water. Rest
iii) Its boiling point is 150°C fi ua
iv) Its freezing point is 0.9°C yntings
v) It decomposes our boiling
LAs Fe
Liq
ace roc
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Chemical Properties. 1X Chemistry
i) Degomposition:
When hydrogen peroxide is exposed to air it decomposes into water and
loxygen
#
Equation:
2H;02 — ” 2H:0 + 0; +Heat \
ji) As Oxidizing Agent: { e
Hydrogen percxide is a sirong oxidizing agent asi
accept electron aclily ¥ oxygen or
Equation: |
%
W202 ~» H20 + O (donation of oxygen)
ie wa, #O8*2H + 20° —__.2H.0 (acceptor of electron
ii) As Reducing Agent: . ‘
: en
or Hydrogen per oxide behave as reducing agention reaction with more powerful
ample: A
oF ois
id on 1202 reduces acid KMnO, solution by.decolonizing the colour of KMnO«
iquation: ;
2KMNOs + 3H,S0, + 5202
K2SO, + 2MnSO, + 8H,0 + 502
Ises: f fe
‘opyl _As Antiseptic: 3
Hydrogen peroxide is\used as a wild antiseptic in mouth wash as well as for
eaning wounds. J
_As Bleaching agent:
7 TaN : A ps 4
Hydrogen peroxide is used as bleaching agent in bleaching materials like silk,
dol, feathers and human hairs. It removes colour from fabrics, hair or other
aterials.
) Restoring Paintings: :
Liquid hydrogen per oxide is used for Restoring painting. Lead carbonate of
intings Blacken when expose to atmosphere.
| As Fuel Component:
Liquid hydrogen per oxide is used for providing oxygen for burning fuel in
ace rockets, It is also used for burning Diesel in engine.
Matric)
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web wre meri 1X Chemis
¥) Other Uses: FO
Itis used in preparation of soaiurn Pr arenie mais used (cuca _—
fed
polymerization reaction.
jing but Comple1
Oxidation and Reduction:
Oxidation and Reduction:
7 ti involve two oppos!
Oxidation and reduetion react ere ‘singly, that is Bry oxidation’
processes. There processes can Ne ee ead i
accompanied by its opposing process reduction and the rence ‘gghrow|id Reduc
Redox Reaction. ~wG Y Xe i oe
Oxidation: } > example:
ne F) ar
i) Oxidation as addition of oxygen: OE ios ‘ 2H
i) dition of oxyden: ‘elements is called oxid:
‘A reaction in which oxygen combine with other wa lation
and it produces oxides. »
\ Asu
Example: on, educed is
S_4Fe + 302 —+ 2Fe203 i Asu
2Mg + Q2 —» 2MgO ‘reas xidize is
. i Ast
ii) Oxidation as removal of Hydrogen: Mes Ast
The removal of hydrogen is also known ‘as oxidation.
:xample
Example: ANE
HSH Cl ea Int
MnO, + 4HC] pg yinGl: # Cle + 2120 av
‘ : si
iii) Oxidation as removal or loss. of electrons: ; ot
‘A reaction whichgecurs by the loss or removal of electrons is called
oxidation. ; oe
Example: fa
eh Sn? + 2e Jecurre
Suter) 28) | of
Al "Al? + 3
% alieved'
Reduction: paver
A'feaction just opposite to oxidation is called Reduction. re in op
repara
i) Reduction as removal of oxyge!
Oz
cygen.
Reduction means the removal of oxygen.
Example: quati
CuO + He ——+ Cu+H,0 a
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IX Chemistry
ji) Reduction as Addition of Hy
eduction also means addition of hydrogen.
xample:
emer HS +Ch —_, $+ 2HCI j
n a g
known) Reduction as gain of electrons: y
A reaction in which substance gains elactron is called reductiOR| yy
Ar?+3% ——> ay
CHE ne ee }
cat “so
Oxidizing and Reducing Agent:
A substance which is oxidizing because it causes Fosse tobe
educed is called as reducing agent. Nacsa
A substance which it self is reduced and éases the other substance to
xidize is called as oxidizing agent. “oR
A substance which gains electronsare called oxidizing agent.
A substance which losses electrons are called reducing agent.
ots
ample: eX
4NH; + 6NO ————» 5N2+6H,0/ t
In this reaction NH, oXidizes-to-Nz-Se-NH, is reducing agent.
In this reactiagNO reduces tolN2,
So NO is oxidizing.agent i
eg et Ozone:
In 1839 Schonbein discovered ozone and in 1886 J. Soret demonstrated that
zone as an allotrope of oxygen.
lecurrence:.
‘Ozone.exists in a layer at a height of about 20 Km above the earth where it is
lieved to protect the earth’s surface from too much ultra violet radiatious of the
un. Very Small amount of ozone produced around electrical machineries when they
-e in operations.
Ozone can be prepared from oxygen by passing electric discharge through
2NH4
‘Ozone dissociates readily forming reaction oxygen t > }
‘
Equation:
O> Pe. aH= agrkstmo!
f
fi) With PbS: a
When ozone reacts with PbS, lead sulphates ntroduct
. Int9
Equation: \X vpand Het
PbS +40; ____, PbSO«+402 equired ir
iii) With HeS: 1. >rocess:
When ozone reacts with HSsulpgurig acid is formed. Fr
7 olume is
Equation: . To
HS + 20) ——————r. ,HzSQ4 4 2 ressure ¢
With SO.: 2quired.
With SO;:
When ozone reacts{witht SO2 sulphur tri oxide fs formed.
Equation:
S02 +O; = $0; + Or
With KI:
When ozone reacts with KI in presence of H2SOx K,SO2and Iz are formed,
Equation:
2K £0; +H2S0, ————> KzSO4tl2* O2+H20
Uses. Jb
i) Itis used in treatment of domestic water.
ij) Itis used as bleaching agent.
It is used in preparation of synthetic fiber.
iv) it is used in pharmaventuals.
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IX Chemistry
Ammonia:
Ammonia is a very important chemical in industry. In nature ammonia is
produced during decay of nitrogenous matter in the absence of air.
pe {Preparation:
| In laboratory ammonia is prepared by heating ammonium chloride wit
Sprected ine
Equation: a: B 4
2NHACI-+ Ca(OH), 2NHs + Cal ep 20
INDUSTRIAL INDUSTRIAL PREPARATION: F i
Bock soscn cn: BOSCH-PROCESS:
introduction: }
In1908, Firtz Haber worked out the reaction.gonditions for the combination of
4zand H: {o make ammonia. Carl Bosh did the necessary engineering work
equired in the process.
2rocess.
In this process a mixture of pure nitrggen and hydrogen in the ration 1:3 by
olume is allowed to react.
To get maximum yield of ammonia the optimum condition of temperature and
ressure are 400 ~ 450°C and 200 — 250 atm. Fe20;, Al203, CaO and K;0 are also
2quired. Ammonia thus obtaliied i is liquefied by cooling.
uation hee
N2* 3H2 400 = 450?C/ 200 - 250atm 2NH3 AH =- 92KJ/mol
pepe nae
formed,
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Physical Properties: ’ vi) With Cz
i) Ammonia is a colourless 9° with pungent smell: pom
ii) Itis a poisonous gas ral uation:
iii) Itis highly soluble in water- a a gure
iv) It is liquefied at room temperature. ‘12 Ises:
; )) Itisu
v) thas density about 0. 8ogmicm. ji) itis u
' , iil) Itis u
Chemical Properties: parse
i) With Air (oxygen) Yai
Ammonia does not burn in air but
Equation: Yee, te oduct
‘4NH; + 302 > 2N2 + 6H20 ~~ troducts
: é In 16
ii) With Water: A —_ hemical.
‘Ammonia is soluble in water to fofmammonia hydroxide.
i aborator
Equation: Ps 5 Nitri
NH; +Hz0 ————» NH.OHS © id.
iii) With Acid: a ‘quation
When ammonia reacts with acid to form salt. KNO
Equation: idustria
‘2NH, +H2S0. “ae (NHs)2 SOs
; * »stwald’
iv) With Chlorine: ~@ Ino
When dtifionthreacts with chlorine, itfirst reduces chlorine and produces
hydrogen chloride, then hydrogen chloride react with excess of ammonia to prod ten td:
ammonium chloride. inge
atinum ¢
Equation: \
‘2NHge 3Cl2 Na+ GHCL quatior
6NH; + 6HC| ————* 6NH, Cl Bil
v) As reducing agent: fen
| “Ammonte reduces heated! copper oxide to free copper metal. Inc
Equation: quatios
3Cu0 + 2NH3 Heat 3Cu + Nz + 3H20 2N
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IX Chemistry
vi) With Carbondioxide:
finmonia reacts with CO, at high temperature to produce Urea.
e ation: i
[fore 1a . (NHa)2 CO + H:0
4
© \se:
i) Itis used in softening temporary hard water, i
ii) Itis used for removing grease and oil.
iii) Itis used as a cooling agent.
iv) It is used in preparing Nitric acid.
v) It is used in manufacture of fertilizers.
Nitric Acid:
atroduction:
ay sally
In 1685 Glauber prepared nitric acid an importantiaboratory and industry
hemical. y
aboratory Preparation: A
Nitric acid is prepared by heating solid potassium nitrate with ionic Sulphuric
sid. , }
‘quation: ‘
KNO3 + H:S0, ———S>—*) KHSO, + HNO3
idustrial Preparation: /°*
istwald’s Method:
In Ostwald process nitric acid is prepared by catalytic oxidation of ammonia.
sroduces § : ,
a to progyfeP td: ‘
In\catalytic chamber firs ammonia react with excess of air in the presence of
atinum catalyst at 600°C and producer NO.
quation:,
4NHy$ 502 Pt 4NO+6H:0 —-95.5KJ/mol
§ 6o"e
tep #2:
In oxidation chamber nitric oxide is mixed with excess air to produce NO2.
quation:
2NO +02
*2NO2
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Step # 3: wrectly dissolved in water to
1 nitrogen per oxide 1s a Equation:
In absorption tower nitrogen P ne
produce nitric acid.
i) With Alh
Equation: ae
‘3NO; + H,0 2HNOs + NO
eat concentratee whictwctn b
ic acid obtain % concentrat
this process is 65:
ii ed in
concentrated further by passing over cone H: Ny
ji) With Mi
Figure: } —
iquation:
} PbO}
v) With M
Wher
Equation:
Cac
“LAs Oxi
Nitric
xidizing p
>mperatur
J2, HNO; b
i) With A
Hot
iquation
c+.
si+
S#
se
Pe
h+
Physical Properties:
i) Nitric'acid isa colourless fuming liquid.
ii) Itha®sourtaste and chocking smell.
iii) (The'boiling point of nitric acid is 83°C
iv) Its freezing point is 41.6°C
v) Its Specific gravity is 1.41
vi) Its Boiling point when 65% pure is 121°C
vii) [8 Gensity is 1.52gm/cm’. Lala
vii) Ris eas in ee wih
Cor
Chemical Properties: BS ne
1) As an Acid: With C
Nitric acid ionizes completely in water. Cu
3ct
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1X Chemistry
Equation:
NOs + H:0 + 1,0" + NO;
Alkali.
When it reacts with alkali form salt and water
\:quation:
HNO, + NaOH
i) With,
*NaOH, +H:0
\
ji) With Metal Oxictes:
When réact with metal oxides forms salt and wave?
equation:
PbO + 2HNO; —__. Pb (NOY), + 1.0
v) With Metal Carbonate:
When react with metal carbonates to form salt’
=quation mt
CaCO, + 2HNO;
* Ca(NOy);+CO;+ ng
+) As Oxidizing Agent:
Nitric acid is a powerful oxidiziNg agent’as it can accept electrons. This
xidizing property depends upon cotini eragtion, nature of reducing agent and
ter.
mperature. Due to this Property it gives variety of productions like NO;, NO, N20,
Jz, HNO2, NH.NO3
® )
i) With Non-Metals: fit F }
Hot nitric acid reacts with non metals to form their oxides and acids.
4
‘quation: #
C+4HNO3\__#" __, ¢0, + 4NO, + 2H,0
Si+4HNO, “"____, si0, + 4NO2 + 2H20
S+4HNO; ) ____,- 0, + 4NO2+ 2H:0
S+6HNO;\ 1,80, + 6NO2 + 2H:0
PSHNO9# ——————>
HsPO4 + 5NO2 + H,0
I, + 10HNO,; ————*_ 2HI0; + 10NO; + 4H,0
ji) With'Metals:
Conc.e as well as did nitric acid oxidize man metals. Cone HNOs librates NOz
as, while reaction of dil. HNO; depend upon nature of reducing agent.
With Copper:
Cu + 4HNO3
» Cu (NOs3)2 +-2NOz + 2H20
3Cu + 8HNO; ____, 3Cu (NO); + 2NO2 + 4H20
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ii) With Lead:
- + 2NO2+ 2H:0
PoeARNG) = PRINCE aio chapter #
3Pb +8HNO; ———> 3PP (NO;)2 + 2N' 7
iii), With Zine: . INTRODUC
ZaaFINOs — 5 Zn (NOs)2* 2NO2 eee . Sulph
Gp eOHINO, ———r 420 (NOs)2* NHNO3* 32 number is 1
es ermicidal ¢
vill) With H,S Q ne
Conc. nitric oxidizes HS to S
Sulph
Equation: ae F) 7
HG 2 HNO; = Sigh Bree “& ip
i } iii)
ix) With FeSQu: ferric sulphate. J
Cone. nitric acid oxidizes ferrous SUIPRCTC toferric $1 . Some
sp, we ees
Equation: \ a on
EERE OHNO; HSON eeemerear nel (SQ + 2NO + 4420 lel rates
x) With SO.: ¢ 2reparatic
Cone. Nitric acid oxidizes SO; f0 H2SQ#0n heating. TRher
7 i) Prep
Equation: . ? ii) Filter
S02 + 2HNOs 2, Hz8O4+ 2NO2 iii) Allov
A bh, iv) Final
Nitration Reaction: Fi ‘
Hot cone. Nitric acid reabts with benzene and replace hydrogen with NO2 aqtructure
this replacement in oxygen compounds is called nitration. lpg
e olecule c
Equation: stahedral
CsHe + HNOs CoHsNO2 + HzO (Dra
5
Aqua Regia: | Monoc
dcone. HClin the ratio of 1:37 calledagy itis.
The mixture of conc. Nitric acid an
regia. This-aqua regia dissolves metals like, gold and librates chlorine. Leagan
Equation:
noel ——+No+Cl, Au+3cl—— AuCh
ii) Allo
iii) Whe
iv) Pou
v) Ren
Suly
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IX Chemistry
Chapter #14 “SULPHUR AND ITS COMPOUNDS”
Sulphur is the second member of Group V1 A. Its symbol is “S”. Its at
gumber is 16 and atomic mass is 32. It is known before 1000 BC for its med
rermicidal effect.
Allotropic Forms of Sulphir: *
Sulphur exist in several allotropic forms out of whl
i) Rhombic Sulphur (<- Sulphur)
fi) Monoclinic sulphur (p- Sulphur) ~
iii) Plastic Sulphur (r— Sulphur)
) Rhombie Sulphur:
Free sulphur exists in nature as rnomble sulph the most stable form of
ulphur. It is obtained as pale yellow crystal aint jon yellow powder.
reparation of Rhombie Sulphur: 4
Rhombie sulphur can be prepared by following steps;
i) Prepare a saturated solution of powdered sulphur in carbon disuiphide.
ii) Filter the solution using filter paper to remove insoluble impurities.
iii) Allow the filtrate to evaporate slowly.
iv) Finally the octahedral ctystals of sulphur (rhombic) are produced.
h NO2a,ttucture of Rhombic Sulphur:
In structure of rhombic sulphur it comprising and molecule in which each
olecule contains and sulphur atom which are covalently bonded and forms an
stahedral structure. ~ @”
(Draw figure44.1.(a) from book Page # 74)
| Monoclinic Sulphur:
called agy Its another crystalline form of sulphur. Itis stable upto 96 to 119°C and finally
sanges into Rhombic sulphur. it comprises of dark yellow needle-like crystal.
ceparation of Monoclinic Sulphur:
Monoclinic sulphur can be prepared as follows,
i) “Heat sulphur so that t converts into molten form.
ii) Allow the molten sulphur to cool slowly.
iii) When crust is formed make two holes in it.
iv) Pour off remaining molten sulphur. *
v) Remove the crust Long needle-like structure are obtained which is monoclinic
Sulphur,
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1X Chem,
Chemical |
Structure of Monoclinic Sulphur:
“ecule, these Ss molecules, unite together with oth
‘ clinic sulphur. ee
Reactior
Itconsists of “Se” M0!
ructure of mor
molecules andi forms necdie— like 55 i
(Draw figure 14.2 from book, page #75) anh
Plastic Sulphur: Fe+s
jij) Plastic Sulphur:
itis a super cooled and non-crystalline form of sulphur A oan
H : Reactio
preparation of Plastic Sulphur :
Plastic sulphur can prepared PY following LoD J M nes
9) Ordinary sulphur is heated upon its boiling Porn Pe saiah
ii) The molten sulphur is poured into very coal Yat ‘s ae
iii) Soft sulphur (plastic) which js like a ball is produ a
(Draw figure 14.3 from book, Page #75) tn
Occurrence’of Sulphur: ‘ ieee ie
This a non-metal and makes Upto 0.1% ofearth’s.crust. An ree state, itig
feo found in Japan and New Zealand, in ) With Ce
found in Sicily, Mexico and U.S.A. 11/5
ron, zinc, lead, copper etc." Pakistany Sulb!
combined form it is fund a sulphates of i
zine, lead, copper, sulphates are 9/52 ortind and its deposits are at Koh —I~ Syijrbon dist
and is Kalat. ¥ c+2
Extraction of Suiphut: s With C.
‘Sulphur can be extracted by a process called “Frasch Process” introducey Sulp
Herman Frasch. |} 28+
Reactic
diameter is drilled in the beds of sulphy, — Sulp
‘An outermost pipe (200M) 1S SUNK upto, S +6
is sunk a little above the deposits,
Frasch Process:
In this process a hole of 30.¢m in
e bore.
Concentric paper is sunk into th
sulphur deposits, The next inner pipe (10cm) I .
‘Super heated water at 175°C at 100 ‘atmospheric pressure is forced through the React
d air at 15 atmospheric pressure is forced throug) Sulp
outermost pipe. Flot compresse'
up molten sulphur and the sulphur (molten), Sa
the innermost pipe which will pump
then solidified in wooden moulds and this sulphur is 99.5% pure. f
3 es of S
Physical Properties of Sulphur: po
Following are the physical properties of sulphur; ii) Itis |
i) Sulphur is a yellow solid. fi) Ig
ii) Itis insoluble in water. paul
iii) It is a non-metal.
iv) It is a bad-conductor of heat and electricity.
v) Its melting point is 113°C to 119°C. Be
ustry. It
din me
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IX Chemistry
chemical Properties of Sulphur:
Othe,
Reaction with Metals:
Supt, Combines with many metals and form their sulphides.
; e+ 5 ae
> Fes
2NA+S —__, Nas
Reign \
Reaction with Non-Metals: :
J
)) With Oxygen:
Sulphur burns in air bright blue flames to form 68
$302 aes SO,
\ |
With Hydrogen: ‘
At 60°C to 66°C sulphur combines with)
H2+S ——_, $
yydrogen t0 from H.S.
te, itis Sean
vand, jy -With Carbo ‘\
akistanyy Sulphur combined with Carbon in air electric furnace to form colourless
= I~ syygrbon disulphide A ul
C+2S ——_. cs, €)
With Chlorin
ntroduceg Sulphur combine with cz on high heating and form di-sulphur-dichloride.
28+Ch “> S.C \
Reaction with Fluorine: }
>f Sulphy, Sulphur combine with Fi2 are high heating to produce sulphur hexafluoride.
ink uptoy, S+6F ——— “SF, fi
a i Reaction with Acids:
ned ll Sulphur oxides (6°S02 when warm with conc. HSO.
Sit 2H2S04 3 380, + 2H20
r(molten, >.<
es of Sulphur:
) [tis Used in manufacturing of Sulphuric acid.
ii) Itis used for bleaching wood pulp.
iii) It i used in vulcanizing rubber.
iv) Itis used as disinfectant in houses.
Sulphuric Acid (H,SO,):
itis the one of the most important compound that is used in laboratory and
ustry. It is the chemical that is used to identify the economy of a country. It is
d in many industries and process.
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Industrial Preparation of H,SOs: o methods. physical Pt
in indugtry HaS0.can be prepared DY pee Eoweose {Follow
contact Process I Lee ITY anc gives Sulphuric acid af i) Pures
Paeeer eet process Ta viemcsle cn iy her
highest purity. iii) It spec
iv) It is cc
Contact Process: 4
Chemical F
Introduction: i d.is pro; ‘Sulph
This process was developed in Germany in 19 vegary an — Perty us,
In 1962, This method comprises of following steps aAsAnA
Sulph
Preparation of SO2: é b H;SO.
in this step SOM is prepared by burning sulphur imgur or by burning Iron
evil a i) With Alk
‘$+ O02 ——» SO % , When
on reo” ‘ and sulphat
NaOt
Purification of SQ2: “eagetg it NaHS
In this step SOM is passed through dust chamber where itis filtered So thay,
dust is removed. ~ Po 1) With Mi
Washing of SO: Se Hi
ashing 0} . is M
‘in this atop SOB is passed through washing chamber where gas is washed) ig0
settle down further impurities) 2 As am
r}
Drying of SO2: ee ley ne
Taghinelepitne posesgeiicc ah of H2SOs in drying chamber, 2/4 Natur
)
Contact Tower: A z
The dried and wastied gas through contact tower where in presence of. , Whe
It
catalyst it is oxidized to SOs. ¥ ye
250; 802, =y20- 280:
a ea Ses cus
Absorption of SOs: ‘ eee
In this step the SOB is produced is absorbed in 91% ion Sulphuric acid to ) Oxidat
produce a very thick oleum. ue
SOs+ HzSQ, H2S207 J
Preparation of H,SO. i) Oxida
In oleum is diluted by dissolving it in water to produce H2SOx of the require HS
concentration. E HS
HySO4+H20 ____, 2H2SQ42- 2Hi
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may IX Chemistry
physical Properties OF H,50,:
Following are the physical properties of H,SO«
i) Pure Sulphuric acid is colourless, ordourless liquid,
ii) The melting point is 10.5°¢
iil) It specific gravity is 4.04
jy) Itis corrosive
Chemical Properties of 50,
Sulphuric acid behave in three different ways.
rty us,
a) As An Acid:
Sulphuric acid isa dibasic acid disassociate when Bissolving inf water.
H:S0.+ 1,0 SS poy igo,
Iron 280,
j) With Alkali:
When Sulphur acid react with alkali it product all of hydrogen sulphate
and sulphate. ag
NaOH + H:S0, + WaHS04+ 1.9)
NaHSO, + NaOH —__ aa
SO thay, ape Nappe +hiQi
+i) With Metal Oxides: eis
When Sulphuric acid reacts with, netal oxides forms metallic salt and water.
+ = a
vaste MSO + H:S04 MgSO, + H,0
) As am Oxidizing Agent!) \
The oxidizing agents property of H2S04 depends upon concentration of air,
‘cid, nature of metal and temperature.
amber, ace
) oxidizing Metal:
© of When/Sulphuric agprescts with metal and dilute and conc. Some produces
alt and H2 ga and'H,03
Zi, + HO ZnSO, + He
CuSi, + Hz
acid to Oxidation of Non Metals:
Hot conc. Sulphuric acid oxides non metals into their oxides and any oxides.
C +2H2SO4 CO; + 280, + 2H,0
i) Oxidation of the compounds:
H2SO, oxides H2S and HI to $ and!
H,S + H,SO, —_, $ + SO, + 2H:0
2HI + HzSO, —__ I + SO + 2H20
cU + 2H.80),
1e requires
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hy,
c) As Drying Agent: me
1
water from varies compound y aD
CHO _, 126+ 111420 at Write a
HCOOH Secor bn. (Tho Ho
Uses of H2SOQx s [ noble f
Sulphuric acid is the most chemicay compound and is. (Gxtensivély used in) Arabi
industries. The progress and the prosperity of any nation can be estiffiated in the ed te
terms of the amounts of Sulphuric acid consumed annually. It is therefore, refusec
bnometer of industrial and economical progress of 2 COUpHY- It’s Important usey ie tru
are as follows 4 rrophe
i) _ Tis used in the manufacture of fertilizers aboubone quarter of H2S04 establi
worked is consumed for she production of two main ea a
in the
produced in th
fertilizers di hydrogen etc: \
us plastic and detergents. i) whet
the Rayon pape?
ii) Itis used too manufacture
iii) Itis used as manufacture in paints and pigments. Es. When |
iv) _ Its used in the making of cellulose film and fabrids- eae
v) Itis usedin steel picking. “ ferven
vi) It is used for Finning of petroleum. (S.A.W
- This n
as “Hi
3 Onwi
id. When
r € circun
found
princi
= School Syste Es
chool Systen, »..
E tojis
XR i 22 oa
esult @ Karachi Board O1g 2:
| fake:
45% students achieved A-1Grad df
45% students achieved A- Grade a
10% students achieved below A-Grade ie
The)
A
of Al
M3
ERT Care School System (montessori to Matric)
5 ‘olony, Karachi. Ph: 021-34 94 0123, 0300/0321-82 32 196
82