B.Sc. Honors Chemistry Syllabus 2023-24
B.Sc. Honors Chemistry Syllabus 2023-24
[AFFILIATED COLLEGES]
PONDICHERRY UNIVERSITY
PUDUCHERRY - 605 014
PONDICHERRY UNIVERSITY
UG BOS in CHEMISTRY
REGULATIONS
1. On completion of the course, students can design and carry out scientific experiments and
also accurately record and analyze the data/results of such experiments. They can explain
why chemistry is an integral activity for addressing environmental problems.
2. Graduates of B.Sc. Chemistry may pursue a career path in pharmaceuticals, food and
beverage companies, cosmetics companies, oil and petroleum companies, mineral
companies, chemical manufacturing companies, clinical facilities etc.
3. They may get placed as a process chemist, industrial chemist, agricultural chemist,
analytical chemist, clinical biochemist, cosmetic chemist, chemical analyst, or a chemistry
teacher.
4. Students can develop skills in problem solving, critical thinking and analytical reasoning
as applied to scientific problems. They can develop ability to communicate the results of
scientific work in oral, written, and electronic formats to both scientific community and
the public community at large.
5. Students will acquire skills to explore new areas of research in chemistry and allied fields
of science and technology.
1. Certificate in Chemistry
2. Diploma in Chemistry
3. B.Sc. Chemistry
4. B.Sc. (Hons.) Chemistry
1. Understanding India
2. Environmental Science/Education
3. Health & Wellness, Yoga Education, Sports, and Fitness
4. Digital and Technological Solutions
4. Basic Eligibility for Admission of Students (Required subjects at +2 level and % of Marks)
5. Total number of Teachers required to handle different subjects (along with their
qualification/specialization)
6. Bridge courses to be organized for other Disciplinary students (Max 10 sessions with zero
credits)
NIL
8. Software or Databases for conduct Computer Lab practicals/major stores for science labs:
10. List of basic Text Books for the entire course (At least one per subject)
a) List of Basic textbooks (for all subjects) --- As per the references cited in the syllabus
b) List of Journals to be Subscribed --- As per the references cited in the syllabus
c) List of Magazines/Newspaper needed --- As per the references cited in the syllabus
d) Approximate Library Budget --- Rs. 50,000 per year
1. Basic Chemistry-I
2. Basic Chemistry Practical-I
3.Basic Chemistry-II
4. Basic Chemistry Practical-II
5. Business Skills for Chemists/Analytical and Clinical Biochemistry
Chemistry (Any one of the two)
4
6. Applied Chemistry/Applications of Computer in Chemistry (Any one
of the two)
7. Introduction to Green Chemistry/Pharmaceutical Chemistry (Any one
of the two)
8. Chemistry in Agriculture/Food and Medicinal Chemistry (Any one of
the two)
Other Courses
Multidisciplinary Course (MDC)
S.No Category Title of Theory Credits
1. Natural Science
2. Physical Science Chemistry in Everyday Life (or)
3
Essentials of Chemistry
3. Social Science
Ability Enhancement Courses (AEC)
S.No Category List of Courses Credits
A. Basic Language& Literature 2
I. English B. Functional Language 2
C. Spoken communication 2
A. Basic Language & Literature 2
II. Indian Language B. Functional Language 2
C. Spoken communication 2
13. Students Activities: (Project work/Internships/Field Studies/Tours/Training/Programs
required to be conducted)
1. Project Work
2. Internships
3. Field Studies
4. Industrial Visit
5. Training program
6. Workshops
Total 25 marks
Total 50 marks
1. Certificate in Major Disciplinary course for exiting students after 1 year with no arrears
provided that they undergo 4 credits Internship during Summer Vacation in the given
stream of skill training.
2. UG Diploma in Major Disciplinary course for exiting students after 2 years with no
arrears provided that they complete 4 Cr Summer Internship for 45 Days.
Passing Minimum: The passing minimum is 40% marks (Internal Assessment + End semester
put together)
17. List of value-added courses/certificates/Diploma co-exists with the main program and add-
ons to be completed by students for qualifying for the degree:
1. Understanding India
2. Environmental Studies
3. Health & Wellness, Yoga Education, Sports, and Fitness:
4. Digital Technologies
Internal External
Project Report Submission 40% 40%
Project Presentation/Viva 10% 10%
Total 50% 50%
B.Sc.ChemistryCurriculum (4 years / 3 years)
Semester I (20Credits)
Theory/
Hrs of
Course Course Code Title of the Course Practical/ Credits
Teaching
Other
Major Disciplinary
Course -1 UCHMJ 1101 General Chemistry-I T 4 5
Mathematics-I / Zoology-I /
Minor Disciplinary
* Botany-I (anyone of the three) T 4 5
Course -1
Course from other department
(Natural Science / Physical
Science / Humanities & Social
Multi-Disciplinary
* science) T 3 4
Course -1
(anyone of the three in each
semester)
Ability Enhancement
* English or Indian Languages T 2 4
Course -1
Skill Enhancement
UCHSE 1100 General Chemistry Practical P 3 4
Course -1
Value Added Course I * VAC-1 Environmental Studies T 2 4
Total 20 30
Major Disciplinary
UCHMJ 2101 Inorganic Chemistry-I T 4 5
Course -3
Major Disciplinary
UCHMJ 2102 Physical Chemistry-I T 4 5
Course -4
Minor Disciplinary
* Physics-I T 4 5
Course -3
Course from other department
(Natural Science / Physical
Multi-Disciplinary * Science / Humanities& social
Course -3 science) T 3 4
(anyone of the three in each
semester)
Ability Enhancement
* English or Indian Languages T 2 4
Course -3
Theory/
Course Course Code Title of the Course Practical/ Credits Hrs of
Other Teaching
Major Disciplinary Course
UCHMJ 2201 Organic Chemistry-I T 4 5
-5
Major Disciplinary
UCHMJ 2202 Physical Chemistry-II T 4 5
Course -6
Major Disciplinary
Course -7 UCHMJ 2203 Basic Analytical Chemistry T 4 5
Minor Disciplinary
* Physics-II T 4 5
Course -4
Ability Enhancement
* English or Indian Languages T 2 4
Course -4
Total 20 30
Theory/
Course Course Code Title of the Course Practical/ Credits Hrs of
Other Teaching
Major Disciplinary
UCHMJ 3101 Inorganic Chemistry-II T 4 5
Course -8
Major Disciplinary
Course -9 UCHMJ 3102 Organic Chemistry-II T 4 5
Major Disciplinary
Course -10 UCHMJ 3100 Organic Chemistry Practical P 4 5
Skill Development
UCHSD3100 MJD15: Summer Internship O 4 6
Course -1
Total 20 26
Theory/
Course Course Code Title of the Course Practical/ Credits Hrs of
Other Teaching
Major Disciplinary
Course -11 UCHMJ 3201 Analytical Chemistry T 4 5
Total 20 25
Theory/
Course Code Hrs of
Course Title of the Course Practical/ Credits
Other Teaching
Major Disciplinary
Course -16 UCHMJ 4101 Inorganic Chemistry-III T 4 5
Major Disciplinary Course -17
UCHMJ 4102 Organic Chemistry-III T 4 5
Major Disciplinary
Course -18 UCHMJ 4103 Physical Chemistry-III T 4 5
Theory/
Practical/ Hrs of
Course Course Code Title of the Course Credits
Other Teaching
Major Disciplinary
Course -19 UCHMJ 4201 Supramolecular Chemistry T 4 5
UCHMJ 4202 Essentials of Nano Chemistry
(any one of the three) UCHMJ 4203 Pericyclic & Organic Photo
Chemistry
Major Disciplinary UCHMJ 4204 Research Methodology
Course -20 T 4 5
UCHMJ 4205 Natural Products &
(any one of the three) Heterocyclic Compounds
UCHMJ 4206 Retrosynthetic Analysis
Semester I
Theory/ Hrs of
Course Course Code Title of the Course Practical Credits Teaching
Minor Disciplinary UCHMI 1101 Basic Chemistry-I T 4 5
Course -1
Multi-Disciplinary Course UCHMD 01 Chemistry in Everyday Life
(any one of the two)
T 3 4
UCHMD 02 Essentials of Chemistry
Semester II
Theory/
Course Course Code Title of the Course Practical/ Credits Hrs of
Other Teaching
Minor Disciplinary
UCHMI 1200 Basic Chemistry Practical-I P 4 5
Course -2
Multi-Disciplinary
UCHMD 01 Chemistry in Everyday Life
Course
(any one of the two) T 3 4
UCHMD 02 Essentials of Chemistry
Semester III
Theory/
Course Course Code Title of the Course Practical/ Credits Hrs of
Other Teaching
Minor Disciplinary Course -
UCHMI 2101 Basic Chemistry-II T 4 5
3
Multi-Disciplinary UCHMD 01 Chemistry in Everyday Life
Course T 3 4
(any one of the two) UCHMD 02 Essentials of Chemistry
Note:Multi-Disciplinary courses in chemistry are common for all the three semesters
Semester IV
Theory/
Course Course Code Title of the Course Practical/ Credits Hrs of
Other Teaching
Minor Disciplinary
UCHMI 2200 Basic Chemistry Practical-II P 4 5
Course -4
Semester V
Theory/
Hrs of
Course Course Code Title of the Course Practical/ Credits
Teaching
Other
UCHMI 3101 Business Skills for Chemists
Minor Disciplinary Course -5
T 4 5
(any one of the two) Analytical and Clinical
UCHMI 3102
Biochemistry
Semester VI
Theory/
Hrs of
Course Course Code Title of the Course Practical/ Credits
Teaching
Other
Semester VII
Theory/
Hrs of
Course Course Code Title of the Course Practical/ Credits
Teaching
Other
Introduction to Green
UCHMI 4101
Minor Disciplinary Course -7 Chemistry
T 4 5
(any one of the two)
UCHMI 4102 Pharmaceutical Chemistry
UCHMI 4103
Minor Disciplinary Chemistry in Agriculture
Course -8 T 4 5
UCHMI 4104
(any one of the two) Food and Medicinal Chemistry
I Year – Semester-I
GENERAL CHEMISTRY – I
Learning Objectives:
To study about atomic structure, chemical bonding and molecular structure
To learn the fundamentals of organic chemistry
To understand stereochemistry and gaseous state
To study about gaseous state and kinetic molecular model
Leaning Outcomes:
Learn the atomic structure, wave particle duality of matter, bonding, and molecular
structures
Understand fundamental concepts in organic chemistry
Learn the structure, shape and reactivity of organic molecules and stereochemistry
Understand the kinetic molecular model of a gas and the behaviour of real gases
Quantum mechanics: Time independent Schrodinger equation and meaning of various terms
in it. Significance of ψ and ψ2, Schrödinger equation for hydrogen atom. Radial and angular
parts of the hydronic wave functions (atomic orbitals) andtheir variations for 1s, 2s, 2p, 3s, 3p
and 3d orbitals (Only graphical representation). Radial and angular nodes and their significance.
Radial distribution functions and the concept of the most probable distance with special
reference to 1s and 2s atomic orbitals. Significance of quantum numbers, orbital angular
momentum quantum numbers ml and ms. Shapes of s, p and d atomic orbitals, nodal planes.
Spin quantum number (s) and magnetic spin quantum number (ms).
Covalent bonding:VB Approach: Shapes of some inorganic molecules and ions on the basis of
VSEPR and hybridization with the following examples – BeCl2, BF3, NH3, SF4, PCl5, SF6 –
Concept of resonance and resonating structures in various inorganic compounds.
MO Approach: Rules for the LCAO method, bonding and anti-bonding MOs and their
characteristics for s-s, s-p and p-p combinations of atomic orbitals, MO treatment of
homonuclear diatomic molecules of O2 and N2 and heteronuclear diatomic molecules such as
CO, NO and NO+. Comparison of VB and MO approaches.
Unit III: Fundamentals of Organic Chemistry (12 Hours)
Physical Effects, Electronic Displacements: Inductive Effect, Electromeric Effect, Resonance
and Hyperconjugation. Cleavage of Bonds: Homolysis and Heterolysis.
Structure, shape and reactivity of organic molecules: Nucleophiles and electrophiles. Reactive
Intermediates: Carbocations, Carbanions and free radicals.
Strength of organic acids and bases: Comparative study with emphasis on factors affecting pK
values. Aromaticity: Benzenoids and Hückel’s rule.
Introduction to types of organic reactions: Addition, Elimination and Substitution reactions.
Unit IV: Stereochemistry (12 Hours)
Conformations with respect to ethane, butane and cyclohexane. Interconversion of Wedge
Formula, Newmann, Sawhorse and Fischer representations. Concept of chirality (up to two
carbon atoms). Configuration: Geometrical and Optical isomerism; Enantiomerism,
Diastereomerism and Meso compounds). Threo and erythro; D and L; cis - trans nomenclature;
CIP Rules: R/ S (for upto 2 chiral carbon atoms) and E / Z Nomenclature (for upto two C=C
systems).
Unit V: Gaseous State: (12 Hours)
Kinetic molecular model of a gas: Postulates and derivation of the kinetic gas equation -
collision frequency - collision diameter - mean free path and viscosity of gases, including their
temperature and pressure dependence, relation between mean free path and coefficient of
viscosity, calculation of σ from η; variation of viscosity with temperature and pressure.
Maxwell distribution and its use in evaluating molecular velocities (average, root mean square
and most probable) and average kinetic energy, law of equipartition of energy, degree of
freedom and molecular basis of heat capacities.
Behaviour of real gases: Deviations from ideal gas behaviour, compressibility factor, Z and its
variation with pressure and temperature for different gases. Causes of deviation from ideal
behaviour. van der Waals equation of state, its derivation and application in explaining real gas
behaviour, calculation of Boyle temperature. Isotherms of real gases and their comparison with
van der Waals isotherms, continuity of states, critical state, relation between critical constants
and van der Waals constants, law of corresponding states.
Reference Books:
• Lee, J.D. Concise Inorganic Chemistry ELBS, 1991.
• Cotton, F.A., Wilkinson, G. &Gaus, P.L. Basic Inorganic Chemistry, 3 rd Ed., Wiley, 2007
• Douglas, B.E., McDaniel, D.H. & Alexander, J.J. Concepts and Models in
Inorganic Chemistry, John Wiley & Sons, 2006.
• Huheey, J.E., Keiter, E.A., Keiter, R.L. &Medhi, O.K. Inorganic Chemistry:
Principles of Structure and Reactivity, Pearson Education India, 2006.
• Graham Solomon, T.W., Fryhle, C.B. &Dnyder, S.A. Organic Chemistry,
John Wiley &Sons (2014).
• McMurry, J.E. Fundamentals of Organic Chemistry, 7th Ed. Cengage Learning India Edition, 2013.
• Sykes, P. A Guidebook to Mechanism in Organic Chemistry, Orient Longman, New Delhi (1988).
• Eliel, E.L. Stereochemistry of Carbon Compounds, Tata McGraw Hill education, 2000.
• Finar, I.L. Organic Chemistry (1964) (Vol. I & II), E.L.B.S.
• Morrison, R.T. & Boyd, R.N. Organic Chemistry, Pearson, 2010.
• Bahl, A. &Bahl, B.S. Advanced Organic Chemistry, S. Chand, 2010.
• Puri B.R., Sharma L.R. and Kalia K.C. Principles of Inorganic Chemistry, Milestone, 2020.
• Arun Bahl, Bahl, B.S. and Tuli G.D. Essentials of Physical Chemistry, S. Chand & Co, 2012.
• Peter Atkins and Julio de Paula, Atkin’s Physical Chemistry 9th Ed., Oxford University Press, 1993.
• Puri B.R., Sharma L.R. and Pathania M.S. Principles ofof Physical Chemistr, Vishal
Publishing Co., 2008.
SEC–1
Course Code: UCHSE 1100 Credits: 3
I Year – Semester-I
GENERAL CHEMISTRY PRACTICAL
Learning Objectives:
Leaning Outcomes:
Able to do different types of titrations and analyze quantitatively the given sample
using the technique of volumetric analysis
Volumetric Analysis
Reference Books:
• Svehla, G. Vogel’s Qualitative Inorganic Analysis, Pearson Education, 2012.
• Mendham, J. Vogel’s Quantitative Chemical Analysis, Pearson, Vogel, A.I., Tatchell, A.R.,
Furnis, B.S., Hannaford, A.J. &Smith, P.W.G.,2009.
Textbook of Practical Organic Chemistry, Prentice-Hall, 5th edition, 1996.
• Mann, F.G. & Saunders, B.C. Practical Organic Chemistry Orient-Longman, 1960.
Major 2 Credits: 4
Course Code: UCHMJ 1201
I Year - Semester - II
GENERAL CHEMISTRY-II
Learning Objectives:
To study chemical energetics
To understand the Chemical Equilibrium, Ionic Equilibria
To understand the principles of qualitative inorganic analysis
To study aboutaliphatic and aromatic hydrocarbons
Leaning Outcomes:
Learn the important principles of thermochemistry and third law of thermodynamics
Understand chemical equilibrium and ionic equilibria
Study the Principles of solubility and Qualitative Inorganic Analysis
Learn in detail about aliphatic and aromatic hydrocarbons
I Year – Semester-II
INORGANIC CHEMISTRY PRACTICAL
Learning Objectives:
To learn how to systematically identify cations and anions present in the given
inorganic mixture.
Leaning Outcomes:
Able to identify cations and anions present in the given inorganic mixture, following a
systematic semi micro analytical technique and also learns how to eliminate the
interfering anion.
Systematic semi-micro qualitative analysis of inorganic mixtures - not more than four ionic
species (two anions and two cations, excluding insoluble salts) out of which one anion being an
interfering radical:
Cations: Lead, antimony, arsenic, tin, bismuth, cadmium, copper, aluminium, chromium, iron,
manganese, zinc, nickel, cobalt, calcium, strontium, barium, magnesium, potassium and
ammonium.
Anions: Carbonate, sulphide, chloride, bromide, iodide, sulphate, nitrate, phosphate, borate,
oxalate, acetate and fluoride.
(using H2S or other methods. Spot tests should be carried out wherever feasible).
Reference Books:
1. Vogel’s Qualitative Inorganic Analysis, Svehla, G. Pearson Education, 2012.
2. An advanced course in Practical Chemistry, Nad, A. K., Mahapatra, B., Ghoshal, A.,
3rd ed., New Central Book Agency: Kolkata, 2007.
3. Vogel’s Textbook of Quantitative Chemical Analysis, Mendham, J., Denney, R. C.,
Barnes, J. D., Thomas, M.,Sivasankar, B., 6th ed.; Pearson Education Ltd: New Delhi,
2000.
Major 3 Credits: 4
Course Code: UCHMJ 2101
INORGANIC CHEMISTRY-I
Learning Objectives:
To learn the chemistry ofhydrogen, hydrides, and s-block elements
To study in detail aboutp-Block Elements
To know the theories of acids, bases & non-aqueous solvents
To learnNuclear Chemistry
Leaning Outcomes:
Get knowledge about the chemistry of hydrogen, hydrides and s-block elements
Understand the chemistry ofp-Block Elements
Know the theories of acids, bases & non-aqueous solvents
Learn important concepts of nuclear chemistry
UNIT-II: p-Block elements –I (Boron, Carbon and Nitrogen group) (12 Hrs)
(a) General characteristics of Boron group elements - Diagonal relationship between B and Si.
Hydrides of Boron – preparation, properties and structure of Diborane. Boron Nitride, Borazine,
Sodium Borohydride and Lithium Aluminium hydride,Boric acid
(b) General characteristics of carbon group elements – Allotropy of carbon, structure of
Diamond and Graphite, catenation, fullerenes. Fluorochlorocarbons, silicates and carbides.
c) General characteristics of Nitrogen group elements. Allotropy of phosphorus, oxides
(N2O,NO2, N2O3,N2O5,P2 O3,P2O5) and Acids of Nitrogen (HNO2,HNO3) & Phosphorus (H3
PO3,H3 PO4,H4 P2O7). Preparation and Structure and uses of Hydrazine, Hydrazoic acid and
Hydroxylamine.
UNIT-III: p-Block elements –II(Oxygen, Halogens and noble gases group) (12 Hrs)
(a) General characteristics of Oxygen group. Allotropy of sulphur - oxides, halides, oxyhalides
of sulphur.Oxyacids (H2SO4.H2SO3,H2S2O7) of sulphur.Persulphuric acids, Dithionic and
Thiosulphuricacid (structure, preparation and properties).
(b) General characteristics of halogen group elements, Oxides and oxoacids of halogens,
Relative strength of oxo acids of the halogens, inter halogen compounds, Pseudo halogens,
Electro positive character of iodine.
c) Chemistry of noble gases:- Position in the periodic table. Occurrence- isolation and
separation of noble gases from atmosphere. Physical properties of noble gases, flurides-
oxyflurides and oxides of xenon (preparation, properties and structure). Applications of noble
gases.
PHYSICAL CHEMISTRY – I
Learning Objectives:
To Study the Solid State and X-ray diffraction studies.
To understand the Chemical Kinetics
To know about the topics Catalysis, Adsorption and Photochemistry.
To study aboutDilute Solutions and Colligative Properties.
To learn about the Phase Equilibrium.
Learning Outcomes:
Learn the Solid State and X-ray diffraction studies.
Understand the kinetics of chemical reactions
Study the Catalysis, Adsorption and Photochemistry.
Know about the Dilute Solutions and Colligative Properties.
Understand the Phase Equilibrium.
UNIT – I Solid State (12 Hours)
(a) Definition of Space lattice , Unit cell , Laws of crystallography –
(i) Law of constancy of interfacial angles
(ii) Law of rationality of indices
(iii) Law of symmetry,symmetry elements in crystals
(b) X-ray diffraction by crystals -– Derivation of Bragg’s equation. Determination of
structures of NaCl,CsCl, KCl, (Laue’s method and powder method).
UNIT-II Chemical Kinetics (12 Hours)
Rate and specific reaction rate; Factors influencing the rate of reaction-concentration,
temperature, pressure, catalyst, solvent and light; Order and Molecularity of reactions;
Derivation of rate constants-zero, first and second order (with equal and unequal concentrations)
reactions; Half-life period; Pseudo order reactions; Determination of order of reactions-
differential method, method of integration and method of half-life period.
Effect of temperature on reaction rate; Arrhenius equation; Activation energy and its
significance; Theory of reactions-Collision theory and Transition state theory.
UNIT-III Catalysis, Adsorption and Photochemistry (12 Hours)
(a) Catalysis
Catalyst and catalysis: Homogeneous and heterogeneous catalysis with examples; Acid-base
catalysis with examples; Enzyme catalysis-general characteristics; Auto catalysis; Derivation of
Michaelis-Menten constant. Theories of catalysis-intermediate compound formation theory and
adsorption theory.
(b) Adsorption
Adsorption-physisorption and chemisorptions; Factors influencing adsorption; Adsorption
Isotherms-Freundlich, Langmuir and BET theories. Application of adsorptions.
(c) Photochemistry
Difference between thermal and photochemical reactions; Laws of photochemistry-Grothus-
Drapper and Stark-Einstein laws; Jablonski diagram; qualitative description of fluorescence
and phosphorescence; Non-radiative processes –internal conversion and inter system crossing;
Quantum yield.
Definition of Phase, Component and Degrees of Freedom; Derivation of Gibb’s phase rule;
Phase equilibria of one component systems – H2O, CO2 and sulphur systems; Two component
systems – Solid-Liquid equilibria- simple eutectic Bi-Cd and Pb-Ag systems; desilverisation of
lead; Solid solutions-compound formation with congruent melting point (Mg-Zn) and
incongruent melting point (NaCl-H2O and CuSO4-H2O) systems.
Liquid-liquid mixtures-ideal liquid mixtures; Raoult’s and Hendry’s law; non-ideal solutions;
partially miscible liquids-phenol-water; trimethylamine-water and nicotin-water systems.
Lower and upper consolute temperature. Effect of impurity on consolute temperature.
Azeotropes-HCl-H2O and ethanol-water systems.
Nernst distribution law-thermodynamic derivations and applications.
Reference Books
1. S.H. Maron and J.B. Lando, Fundamentals of Physical Chemistry, Macmillan limited,
New York, 1966.
2. B.R. Puri, L.R. Sharma and M.S. Pathania, Principles of Physical Chemistry, 46th Edi-
tion,Vishal Publishing Company, New Delhi, 2013.
3. Gurdeep Raj, Advanced Physical Chemistry, 35th Edition, Goel Publishing House, Mee-
rut, 2009.
4. P.W. Atkins, Physical Chemistry, 7th edition, Oxford university press, 2001.
5. S.K. Dogra and S. Dogra, Physical Chemistry Through Problems, New age internation-
al, 4th edition 1996.
6. Gilbert. W. Castellan, Physical Chemistry, Narosa publishing house, third edition 1985.
7. Irving M. Klotz and Robert M. Rosenberg, Chemical Thermodynamics, John Wiley and
sons, Inc. 1994.
8. J. Rajaram and J.C. Kuriacose, Thermodynamics, Shoban Lal Nagin Chand and CO.
1986.
9. K. L. Kapoor, A Textbook of Physical chemistry, (volume-2 and 3) Macmillan, India Ltd,
1994.
10. K. Laidler, Chemical Kinetics, 3rd Edition, Pearson Education, New Delhi, 2004.
11. K.K. Sharma and L.K. Sharma, A Textbook of Physical Chemistry, 5th Edition, Vikas
Publishing House, New Delhi, 2012.
12. K.L. Kapoor, Physical Chemistry Vol. 3&5, Macmillan Publishers, Noida, 2004.
13. G.K. Vemula Palli, Physical Chemistry, Prentice Hall of India, New Delhi, 1997.
SEC-3 Credits: 3
Course Code: UCHSE 2100
II Year – Semester-III
PHYSICAL CHEMISTRY PRACTICAL
Learning Objectives:
To learn laboratory experiments in order to understand the concepts of physical changes
in chemistry
To learn how to determine the enthalpy change, distribution co-efficient and colligative
properties
Leaning Outcomes:
Demonstrate laboratory skills for safe handling of the equipment and chemicals
Experiment set-up and recording the data from the experiments applying the principles
learned in physical chemistry theory course
Reference Books:
1. Basic Principles of Practical Chemistry, Venkateswaran V, Veeraswamy R,
Kulandaivelu, A.R., 2nd ed., Sultan Chand, New Delhi, 2012.
2. An advanced course in Practical Chemistry, Nad, A. K., Mahapatra, B., Ghoshal, A.,
3rd ed., New Central Book Agency: Kolkata, 2007.
3. Vogel’s Qualitative Inorganic Analysis, Svehla, G. Pearson Education, 2012.
4. Vogel’s Textbook of Quantitative Chemical Analysis, Mendham, J., Denney, R. C.,
Barnes, J. D., Thomas, M.,Sivasankar, B., 6th ed.; Pearson Education Ltd: New Delhi,
2000.
5. Practical Organic Chemistry, Manna, A.K., Books and Allied: India, 2018.
6. Vogel’s Textbook of Practical Organic Chemistry, Furniss,B. S., Hannaford, A.
J.,Smith, P. W. G., Tatchell, A.R., 5th ed., Pearson: India,1989.
Major 5 Credits: 4
Course Code: UCHMJ 2201
II Year – Semester - IV
ORGANIC CHEMISTRY – I
Learning Objective:
To study about the Alkyl and Aryl Halides
To learn the chemistry of alcohols and phenols
To understand about the Carbonyl Compounds
To study about the Organic Compounds of Nitrogen
To learn about the Heterocyclics
Learning Outcomes:
Learn about the chemistry of Alkyl and Aryl Halides
Understand the chemistry of alcohols and phenols
Know about the Carbonyl Compounds and their reactions
Study about the Organic Compounds of Nitrogen
Learn the chemistry of Heterocyclic compounds
Alkyl halides:Preparation from alkenes and alcohols. Reactions - hydrolysis, nitrite & nitro
formation, nitrile and isonitrile formation, Williamson’s synthesis, Elimination vs Substitution
Aryl halides:Preparation of chloro-, bromo- and iodo-benzenes from phenol, Sandmeyer and
Gattermann reactions. Reactions of aryl halides: Aromatic nucleophilic substitution
(replacement by –OH group and effect of nitro substituent. Benzyne mechanism:
K(Na)NH2/NH3.
Reactivity and relative strength of Carbon-Halogen bond in alkyl, allyl, benzyl, vinyl and aryl
halides.
Alcohols:Preparation of primary, secondary and tertiary alcohols using Grignard reagent, ester
hydrolysis, reduction of aldehydes, ketones, carboxylic acids and esters. Reactions with sodium,
HX (Lucas Test), esterification, oxidation (with PCC, alk. KMnO 4, acidic dichromate, Con.
HNO3). Oxidation of diols - Pinacol-Pinacolone rearrangement.
Phenols:Preparation bycumene hydroperoxide method, from diazonium salts. Reactions -
Electophilic substitution - nitration, halogenations and sulphonation. Reier-Tiemann reaction,
Gattermann-Koch reaction, Houben- Hoesch condensation, Schotten Baumann reaction. Acidic
character of phenol, comparative strength of alcohol and phenol.
Molecular Orbital picture and aromatic characteristics of pyrrole, furan, thiophene and
pyridine. Methods of synthesis and chemical reactions with emphasis on the mechanism of
electrophilic substitution reaction, mechanism of nucleophilic substitution reactions in pyridine
derivatives. Comparison of basicity of pyridine, piperidine and pyrrole. Introduction to
condensed five- and six-membered heterocyclics. Preparation and reaction of indole, quinoline
and isoquinoline with special reference to Bisler-Napieralski synthesis. Mechanism of
electrophilic substitution reactions of indole, quinoline and isoquinoline.
Reference Books:
• Kotz, J.C., Treichel, P.M. & Townsend, J.R. General Chemistry, Cengage Learning India Pvt.
Ltd.: New Delhi (2009).
• Petrucci, R.H. General Chemistry, 5th Ed., Macmillan Publishing Co.: New York (1985).
• Morrison, R. T. & Boyd, R. N. Organic Chemistry, Dorling Kindersley (India) Pvt. Ltd.
(Pearson Education).
• Finar, I. L. Organic Chemistry (Volume 1), Dorling Kindersley (India) Pvt. Ltd.
(Pearson Education), 1964.
• Finar, I. L. Organic Chemistry (Volume 2), Dorling Kindersley (India) Pvt. Ltd.
(Pearson Education), 1964.
• Nelson, D. L. & Cox, M. M. Lehninger’s Principles of Biochemistry 7th Ed., W. H. Freeman,
2017.
• Berg, J.M., Tymoczko, J.L. &Stryer, L. Biochemistry, W.H. Freeman, 2015.
• R.T. Morrison & R.N. Boyd: Organic Chemistry, 7th Ed., Prentice Hall, 2010.
• Peter Sykes: A Guide Book to Mechanism in Organic Chemistry, 6th Ed., Orient Longman,
2003.
• ArunBahl and B. S. Bahl: Advanced Organic Chemistry, S. Chand, 2012.
Major 6 Credits: 4
Course Code: UCHMJ 2202
II Year - Semester - IV
PHYSICAL CHEMISTRY-II
Learning Objectives:
To Study about Electrochemistry
To learn the Elementary Quantum Mechanics
To understand the molecular spectroscopic methods: microwave, IR, Raman and
electronic spectroscopy.
To use molecular spectroscopy in studying the physical properties and molecu-
lar structure of compounds
Learning Outcomes:
Get good knowledgeabout Electrochemistry
Learn the Elementary Quantum Mechanics
Understand the molecular spectroscopic methods: microwave, IR, Raman and
electronic spectroscopy.
Use molecular spectroscopy in studying the physical properties and molecular
structure of compounds
UNIT-I Electrochemistry-I (12 Hours)
Electrical transport-conduction in metals and in electrolyte solutions; specific conductance;
equivalent conductance; measurement of equivalent conductance; variation of equivalent
conductance with dilution; migration of ions and Kohlrausch law; Ostwald dilution law-uses
and limiatations; Debye-Huckel-Onsager equation for strong electrolytes (derivation not
required).
Transport number; determination by Hittorf method and moving boundary method;
determination of degree of dissociation; determination of Ka of acids; determination of
solubility product of sparingly soluble salts; conductometric titrations.
II Year - Semester - IV
BASIC ANALYTICAL CHEMISTRY
Learning Objectives:
To study about laboratory glasswares, cleaning methods and first aid procedures.
To learn stoichiometry and concentration systems
To understand the principles of volumetric analysis
To learn statistical evaluation of analytical data
To study gravimetry and thermo analytical methods
Leaning Outcomes:
Learn about laboratory glasswares, cleaning methods and first aid procedures
Understand stoichiometry and concentration systems
Acquire knowledge about the principles of volumetry
Gain understanding about statistical evaluation of analytical data
Understand gravimetry and thermo analytical methods
(a) Definition of the terms primary standard and secondary standard solutions — Equivalence
point and end point of titrations, — Types of titrations — Calculations involving
volumetric titrations.
(b) Acid - Base Titrations : Derivation of titration curves for strong acid Vs strong base
and weak acid Vs strong base titrations — Theory of acid-base indicators.
(c) Redox Titrations :Nernst equation — Theory of redox indicators — Types of redox
indicators.
(d) Complex Formation Titrations: Chelating agents – EDTA- Theory of metallochyromic
indicators – Titrations involing EDTA – Types of EDTA titrations.
(e) Precipitation Titrations: Argentometric titrations – indicators for titrations involving
silver nitrate.
UNIT-III (12 Hrs)
Reference Books:
Minor 1
Credits: 4
Course Code: UCHMI 1101
I Year – Semester-I
BASIC CHEMISTRY – I
Learning Objectives:
To Study classification, nomenclature and some fundamentals of organic chemistry.
To Study isomerism in organic compounds and conformational analysis
To Study the stoichiometry and some basic concepts of chemical equilibrium
To Study radioactivity and its applications
To study carbohydrates
Leaning Outcomes:
Learn the Classification and IUPAC nomenclature of organic compound
Understand the hybridization in organic compounds, dipole moments and charged spices
Acquire knowledge about isomerism in organic compounds and learn how to name them
Gain understanding about on cepts of chemical equilibrium, acids and bases, pH and
buffer
Understand radioactivity and its applications
Classification and IUPAC nomenclature of organic compound, Hybridization (sp3, sp2 and sp) in
organic compounds, localized and delocalized chemical bonds, Hydrogen bonding. Dipole
moments in organic molecules, homolytic and hetrolytic bond cleavage, electrophiles,
nucleophiles and free radicals, carbocations and carbanions.
Structural and Stereo isomerism, Geometrical isomerism, Cis, trans isomers, E and Z
nomenclature of simple compounds; Optical isomerism, optical activity, specific rotation,
enantiomers, diastereomers, and meso compounds. R, S configuration in organic molecules with
single symmetric centre. Conformers, Newman and sawhorse projection formulae,
conformational analysis of ethane, n-butane and cyclohexane.
Unit III: Stoichiometry (12 Hrs)
Mole and equivalent concepts, concentration units, molarity, molality, percentage, ppm, and ppb.
Types of solutions, stoichiometric calculations.
Basic concepts of chemical equilibrium, equilibrium constants. Concepts of acids and bases.
Ionisation of weak acids and weak bases. Hydrogen ion concentration, pH of acids and bases.
Buffer solutions, Henderson’s equation of buffer. Physiological buffers.
Unit-IV: Radioactivity (12 Hrs)
Properties of α, β and γ-radiations, rate of disintegration, half life period, nuclear fission and
fusion, fertile and fissile nuclei, radioactive isotopes, nuclear reactions and group displacement
law, Application in medicine, agriculture, geology and industry. nuclear reactors- working
principle. Neutron activation analysis.
Classification, preparation, properties and structures of glucose, fructose, and sucrose (structural
elucidation not required), mutarotation, epimers and anomers. Polysaccharides, uses of starch
and cellulose (structural elucidation not required) test for sugars.
References Books:
1. Text Book of Organic Chemistry by P.S. Soni, 29th Ed., 2012.
2. Principles of Physical Chemistry by Puri and Sharma, 2020.
3. Allied Chemistry – I by K.M.Tajun Meera Begum and N.M.I.Alhaji, 2016.
4. Advanced Organic Chemistry by Bahl and Arun Bahl, 2012.
5. Modern Inorganic Chemistry by R.D. Madan, 1987.
6. Principles of Inorganic Chemistry by Puri and Sharma, 2020.
7. Physical Chemistry by Bahl and Tuli, 28th Ed., 2020.
8. Analytical Chemistry by Gopalan et al, Sultan Chand & sons, 2003.
Minor 2 Credits: 4
Course Code: UCHMI 1200
I Year – Semester-II
Learning Objectives:
To learn to do titrimetric experiments
To calculate the concentrations of unknown solutions
To determine the melting and boiling points of organic compounds
Leaning Outcomes:
Understand basic principles involved in titrimetric analysis and compare the
methodologies of different titrimetric analysis
Develop the skill to estimate the amount of a substance present in a given solution
Measure the melting point and boiling points of organic compounds and compare with the
literature values
1. Determination of melting point of organic compounds using water bath (m.pt.< 100 oC).
2. Determination of boiling point of organic substances like ethanol, cyclohexane, toluene,
benzene etc.,
3. Determination of viscosity of the given liquid using Ostwald’s Viscometer.
4. Purification of organic compounds by recrystallisation.
a) Aromatic substances from hot water; (b) Naphthalene from ethanol
Reference Books:
1. Basic Principles of Practical Chemistry, Venkateswaran, V.,Veeraswamy, R., Kulandivelu,
A.R.,2 nd ed., Sultan Chand &Sons: New Delhi, 1997.
2. An advanced course in Practical Chemistry, Nad, A. K.. Mahapatra, B.. Ghoshal, A.., 3rd
ed., New Central Book Agency: Kolkata, 2007.
3. Vogel’s Textbook of Quantitative Chemical Analysis, Mendham, J., Denney, R. C., Barnes,
J. D., Thomas, M.,Sivasankar, B., 6th ed.; Pearson Education Ltd: New Delhi, 2000.
Minor 3 Credits: 4
Course Code: UCHMI 2101
II Year – Semester-III
BASIC CHEMISTRY – II
Learning Objectives:
To Study thermodynamics and chemical kinetics
To Study chromatography and solid state
To Study amino acids, proteins and enzymes
To Study polymers and dyes
To study nucleic acids and drugs
Leaning Outcomes:
Understand the concept of heat, work, Internal energy and enthalpy
Learn about separation techniques of organic compounds, bonding in metals,
semiconductors and conductors
Gain knowledge on building blocks of proteins and DNA and dyes
Get an idea about the pharmaceutical drugs analgesics and antipyretics like paracetamol
and aspirin and also about pigments and dyes and its applications.
First Law of Thermodynamics, Statement, concepts of heat, work and internal energy, Enthalpy
and heat capacity, exothermic and endothermic reactions, Second Law of Thermodynamics,
spontaneous and non spontaneous processes, entropy concept. Chemical Kinetics: Rate of
reaction, Factors affecting the rate of reaction, order and molecularity, examples for zero, first
and second order reaction.
Polymers, Preparation and uses of nylon (6,6), Terylene, polythene, polyvinyl chloride, natural
rubber and synthetic rubber (Buna-S rubber and neoprene) Vulcanization; Dyes, Modern
classification and examples (Indigo, congo red, malachite green, Alizarin and Phenolphthalein)
Nucleic acid – Structure of DNA and RNA, brief account of m-RNA, t-RNA and r-RNA –
differences between DNA and RNA.
Drugs, Antiseptic (Dettol), Antipyretic (Paracetamol), Analgesic (Aspirin), Antimalarial
(Quinine), Antibiotic (Penicillin), Sulfa Drug (Sulfadiazine) - Structural elucidation not
required.
Reference Books:
Learning Objectives:
To perform analysis to identify the functional group in an unknown organic compound
performing a systematic analysis
To learn to separate organic compounds using simple methods and chromatographic
techniques
Leaning Outcomes:
Observe the physical state, odour, colour and solubility of the given organic compound.
Identify the presence of special elements and functional group in an unknown organic
compound performing a systematic analysis
Compare between mono and dicarboxylic acids, primary, secondary and tertiary amines, mono
and diamides, mono and polyhydric phenols, aldehyde and ketone, reducing and non-reducing
sugars and explain the reactions behind them
Prepare a solid derivative with respect to the identified functional group
Learn to separate the organic compounds by simple methods and chromatography
Other Experiments:
Learning Objectives:
To study functional food additives and food adulteration
To study soaps and detergents, manufacturing process and environmental hazards
To study chemical composition of cosmetics and perfumes
To study the chemical nature of glasses, ceramics and plastics in daily use
Leaning Outcomes:
Learn about food adulteration, food additives and artificial sweeteners, saccharin,
cyclomate and aspartate in the food industries
Understand the chemistry of soaps and detergents and their action
Know about the ingredients in commonly used cosmetics and perfumes
Gain knowledge about glasses and ceramics and their properties
Learn the nature of the plastics used in everyday life and natural substitution for plastic
Functional food additives and its importance, food adulteration, detection of food adulterations,
food safety laws and fssai regulations. Food colours-permitted and non-permitted – Flavours –
natural and synthetic, artificial sweeteners, toxic effect of additives.
Cosmetics and perfumes – classification, ingredients and regulations, bathing oils, face creams,
talcom powder, skin products, hair dyes, shaving cream, shampoo, conditioners, nail polish,
deodorants, antiperspirants, oral hygiene products, toxic effect of cosmetics.
Reference Books:
1. Food – The Chemistry of its components, T.P. Coultate,. Royal Society of Chemistry
London, 2001.
2. Engineering Chemistry, Shashi Chowla, DanpatRai & Co., 2017.
3. Industrial Chemistry, B.K. Sharma, Krishna Prakashan Publishers, 2012.
4. Understanding Chemistry, CNR Rao, Universities Press, 1999.
5. Engineering Chemistry, Jain and Jain, Darpat Rai Publication, 17 th Ed., 2015.
6. Chemistry of cosmetics, Kumari R, Prestige publications, 2018.
Multi-Disciplinary Credits: 3
Course Code: UCHMD 02
Semesters-I, II & III
2. ESSENTIALS OF CHEMISTRY
Learning Objectives:
To learn about structure of atoms and periodic classification of elements
To study about radiations and nuclear chemistry
To know the chemistry of polymers
To study about vitamins and chemistry involved in some important biological process
To learn about some application oriented chemicals
Leaning Outcomes:
Learn about atomic structure, periodic properties of elements and periodic classification
Understand about radiations and the chemistry involved in nuclear reactions
Know about polymer chemistry and few important polymers
Gain knowledge about vitamins and chemistry of some important biological process
Learn the chemistry of some application oriented chemicals
Reference Books:
1. M. C. Day and J. Selbin,“ Theoretical InorganicChemistry”, East West Press, 2nd Edition,
2008.
2. H. J. Arniker,“ Essentials of NuclearChemistry, New Age International Publishers, 2011.
3. B.K. Sharma “EnvironmentalChemistry”, Goel Publishing House, 2014.
4. Solomons- John- Wiley, “Fundamentals of OrganicChemistry” 4th Edition, 1994.
5. F.A. Carey, Mc. Graw Hill ,“Organic Chemistry”, 4th Ed., 2000.
6. I.L Finar,“Organic Chemistry”, Vol. 1Longman, 2002.
7. K. S. Tewari, N. K. Vishnoi,“A Text book of OrganicChemistry” 4th Ed., 2017.
8. M.K. Jain,“ Principles of OrganicChemistry”, S. Nagin publishers, 1978.