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Chemistry 241222 094316

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34 views6 pages

Chemistry 241222 094316

Uploaded by

rajaniket1235
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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SET-A

KENDRIYA VIDYALAYA SANGATHAN, PATNA REGION


2nd Pre Board Examination- 2024-2025
SUBJECT: - CHEMISTRY (043) Theory
Marking Scheme
[Time: 3ℎrs.] Class –XII [Max.Marks-70]

Question No. 1 to 16 are of 1 marks each.

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
c a c b c a d b a d c b d a c a

Q. No. Value Points/Expected Answer Marks


SECTION-B
Q17. E0 Cell = 0.34-(-2.37) = 2.71V ½
E cell =2.71 -0.0591/n log [Mg+2]/[Cu+2]
1
=2.71-0.0591/2 log (0.001)/(0.0001)
E cell = 2.68 V ½
OR
In the case of CH3COOH, which is a weak electrolyte, the No. of ions increase on
dilution due to an increase in degree of dissociation. In the case of strong electrolyte 1+1
the number of ions remains the same but the interionic attraction decreases.
Q18. R=K[A]n ---------------- (i) ½
3R=K[9A]n ------------- (ii)
Dividing equation(ii)by (i),we get 3 ½
=9n
3 = 3 2n
½
1 = 2n
n =½ ½
order of the reaction = ½
Q19. 1+1

Q20. (a) Add NaHCO3 to each. Phenol will not react, benzoic acid will give brisk 1+1
effervesce due to CO2.
(b) Add I2 and NaOH. Ethanal will give yellow ppt. of iodoform, whereas 1-
Propanol will not give yellow ppt.

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Q21. Deficiency of vitamin A leads to Xerophthalmia and night blindness, whereas 1+1
deficiency of vitamin C leads to scurvy and bleeding of gums. Carrot, fish liver oil,
butter and pulses are the sources of vitamin A whereas citrus fruits, amla and green
leafy vegetables are the sources of vitamin C.
SECTION-C
Q22. A=K2MnO4 B= KMnO4 1+1+1

On heating, 2KMnO4 → K2MnO4 + MnO2 + O2


Q23. (i) It is because ethers are not associated with intermolecular H- bonding, whereas 1
ethanol is associated with intermolecular H-bonding.
(i) (ii) In case of phenoxide ion, the negative charge is present on one 1 +1
electronegative oxygen atom and the lesser electronegative carbon atoms.
The contribution of resonance structures towards resonance stabilization of
phenoxide ion is less. In case of carboxylate ion, the negative charge is
present on two electronegative oxygen atoms.
The contribution of resonance structures towards resonance stabilization of
carboxylate ion is more. Hence, the carboxylate ion is more resonance stabilized
than the phenoxide ion. Due to this, carboxylate ion is more stable than phenoxide
ion. Higher stability leads to greater acidic strength.
(Correct resonance structures of phenoxide ion and carboxylate ion)
Q24. Fe2+ + 2e − → Fe ½
2𝐹
(1𝑚𝑜𝑙)
56𝑔 𝐹𝑒 𝑟𝑒𝑞𝑢𝑖𝑟𝑒𝑠 2 × 96500 𝐶
1
2 × 96500 × 2.8
∴ 2.8 𝑔 𝐹𝑒 𝑟𝑒𝑞𝑢𝑖𝑟𝑒𝑠 = 9650 𝐶 ½
56
𝑄 9650
𝑄 = 𝐼𝑡, ∴ 𝑡 = = = 4825 𝑠𝑒𝑐.
𝐼 2
1
𝑊𝑧𝑛 𝐸𝑧𝑛 𝑊𝑍𝑛 65⁄2
𝑁𝑜𝑤, = ⇒ = ⇒ 𝑊𝑧𝑛 = 3.25𝑔
𝑊𝐹𝑒 𝐸𝐹𝑒 2.8 56⁄
2
Q25. (a) t60% =2.303/k log [R]0/40[R]0/100 ½+½
=2.303/k(log10-log4)
k=2.303/30(1.0000-0.6021)
k=2.303/30x0.3979=3.05x10 min-1
½+½
t1/2=0.693/k
t1/2=0.693/3.05x10-2min-1
=22.72 min
(b) For effective collisions:
i) The molecules must collide with minimum energy i.e. threshold energy ½+½
ii) Proper orientation of molecules
Q26. (a) 3,4,4-Trimethylpent-2-ene is the major product. 1+1+1
(b) In the first step, the ethanol or ethyl alcohol is reacted with hydrochloric acid in
the presence of zinc chloride as a catalyst to form chloro ethane and water. In the

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second step, the chloro ethane is reacted with silver fluoride to form ethyl fluoride as
a product.
𝑍𝑛𝐶𝑙2 𝐴𝑔𝐹
𝐶𝐻3 𝐶𝐻2 𝑂𝐻 + 𝐻𝐶𝑙 → 𝐶𝐻3 𝐶𝐻2 𝐶𝑙 → 𝐶𝐻3 𝐶𝐻2 𝐹
(c) The ionization of aqueous KOH produces hydroxide ions which are strong
nucleophiles. Hence, alkyl chlorides undergo substitution to form alcohol.
Alcoholic KOH solution gives alkoxide ion which is a strong base. It
abstracts β hydrogen atom of alkyl chloride. A molecule of HCl is eliminated and an
alkene is formed.
Q27. Alkaline KMnO4 ,Oxidation 1+1+1
(a) CH3CH2CH2OH + 2 [O] ----------------------------------------------> CH3CH2COOH + H2O

(b)

(c)

OR

(a) 1+1+1

(b)

(c) CH3- CH2- CHOH + NaOH → CH3- CH2- CHONa


CH3- CH2- CHONa + CH3 -CH2 -CH2 Br → C2H5- O- CH2- C2H5 + NaBr
Q28. (a) In an aqueous medium, Cu2+ is more stable than Cu+. This is because although 1+1+1
energy is required to remove one electron from Cu+ to Cu2+, high hydration energy of
Cu2+ compensates for it. Therefore, ion in an aqueous solution is unstable. It
disproportionates to give Cu2+ and Cu.
2Cu+(aq)→Cu2+(aq)+Cu(s)
(b) The hydration or lattice energy is more than sufficient to remove the only electron
present in the d-orbital of these ions. The ions in d1 configuration tend to lose one
more electron togetintostabled0 configuration.
(c)The electrode potential values for Mn2+ /Mn is more negative than expected due to
greater stability of half-filled d-subshell (d5) in Mn.
SECTION-D
Q29. (i) 1

1
(ii) C6H5CH2NH2 + CHCl3 +KOH→C6H5CH2NC 1+1

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(iii)C6H5N2Cl +CuCN →C6H5CN
C6H5CN + H2O→ C6H5COOH
OR 1+1
C6H5NH2+ NaNO2 +HCl→ C6H5N2Cl

Q30. (i) Maximum boiling azeotropes. 1


(ii) D will have lower vapour pressure because it has highest boiling point. 1
(iii) M= no. of moles x1000/volume of solution in ml
1+1
=6.02x1022x1000/6.02x1023x50
=2M
OR
πV=nRT 1
π x 0.1L=5x0.0821x300/60 1
=24.63/1.2=20.52 atm 1+1
SECTION-E
Q31. A= CH3 -CH2 -CH2 - COO -CH2 -CH2 –CH-CH3 1+1
B=CH3 -CH2 -CH2 -COOH
C= CH3 -CH2 -CH2-CH2-OH
CH3CH2CH2 COOCH2CH2CH2CH3→ CH3-CH2-CH2-COOH + CH3-CH2-CH2-CH2-OH
Dehydration
ConC. H2SO4
CH3 − CH2−CH2 − CH2OH −−−−−−→ CH3 − CH2 − CH = CH2
ChromiC aCid
CH3 − CH2−CH2 − CH2OH −−−−−−→ CH3 − CH2 − CH2 − CH2 − COOH 1+1+1
(i)Cl2, Red P,(i i)H2O
CH3CH2CH2CH2COOH −−−−−−−−−−→ CH3 − CH2 − CH2 − CH(Cl) − COOH
OR
(a) 6-Chloro-4-ethylhexan-3-one
(b) Butanone < Propanone< Propanal < Ethanal
(c) (i)In 2,2,6-Trimethylcyclohexane, there is stearic hindrance of three methyl
1+1+1
groups therefore, it does not form cyanohydrin in good yield as compared to
cyclohexanone which does not have stearic hindrance.
(ii) It does so that ester formed does not get hydrolysed to give acid and alcohol back.
It is done so as to shift equilibrium in forward direction.
(d) CH3COCH3 ---(LiAlH4) → CH3-CH (OH)-CH3 𝑐𝑜n𝑐.𝐻2𝑆𝑂4 → CH3 -CH= CH2 1+1

Q32. (a)(i) Glucose cyanohydrin (ii) n-hexane (iii) Gluconic acid 1+1+1
(b)It indicates that –CHO group of glucose is not free, but it is present in cyclic 1
hemiacetal form.
(c) (i) Monosaccharides: Glucose
(ii) Oligosaccharides: Sucrose 1
(iii) Polysaccharides: Starch
OR
(a) (i) Due to presence of zwitter ion amino acids react with acid and acid react with
1
amine thus they show amphoteric nature.
(ii) Amino acid exists as a dipolar ion. On electrolysis in acidic medium it changes to
positive ion so it migrates towards cathode while on electrolysis in basic medium it 1
changes to negative ion so it migrates towards anode. 1
(b)Peptide linkage, -CONH2-
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(c)Uracil 1
(d) Phosphodiester linkage 1

Q33. (a) (i) [Co(NH3)5SO4]Cl + AgNO3(aq) →AgCl(s) + [Co(NH3)SO4]NO3 1


‘A’ White ppt
[Co(NH3)5Cl]SO4 + BaCl2 (aq) → BaSO4(s) + [Co(NH3)5Cl]Cl2
‘B’ White ppt
1
(ii) Ionisation isomerism
(iii) ‘A’ is penta ammine sulphatocobalt(III)chloride
‘B’ is penta ammine chloridocobalt(III)sulphate 1
(iv)The oxidation state of Ni is zero in [Ni(CO)4] but it is +2 in [NiCl4]2-,
As Ni(Z = 28)[Ar] 3d8 4s2 2
Show complete hybridization

OR
(a) t2g eg0
4 1+1+1+1+1
(b) Ethylene diamine (en) is a bidentate ligand
(c) EDTA (Ethylene diamine tetraacetate ion)
(d) Fe2+ : no. of unpaired e- is 4
So, μ = √𝑛(𝑛 + 2) BM = √24 𝐵𝑀 = 4.86 𝐵𝑀
(e) Dichloridobis(ethane-1,2-diamine)cobalt(III)nitrate

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