MSC Chemistry AIU 2024
MSC Chemistry AIU 2024
Semester 1
Theory
Course Topic L T P Credit Theory Internal Practical Total
Code Marks Marks Marks Marks
24CH101 Inorganic Chemistry- I 4 0 0 4 70 30 0 100
Detailed Syllabus
INORGANIC CHEMISTRY-I
Code: 24CH101
Max Marks: 70
Text Book:
1. Cotton, F.A.; Wilkinson Advanced Inorganic Chemistry, 6th Sons, 1999. edition, John Wiley& Sons,
1999
2. Huheey, James E. Inorganic Chemistry: Principles of Structure and Reactivity, 4th edition, Harper
Collins College Publishers, 1993.
3. Greenwood, N.N. and Earnshaw, A. Chemistry of the Elements, 2nd edition, Butterworth-Heinemann,
A division of Read Educational & Professional Publishing Ltd., 2001
4. Lever, A.B.P. Inorganic Electronic Spectroscopy, 2nd edition, Elsevier Science Publishers B.V., 1984.
5. Carlin, Richard L. and Duyneveldt, A. J. Van Magnetic Properties of Transition Metal Compounds,
Inorganic Chemistry Concepts 2, Springer-verlag New York Inc., 1977.
Reference Books:
1. Shriver, D.F.; Atkins, P.W. Inorganic Chemistry, 1st edition, Oxford University Press, 2006.
2. Earnshaw, A. Introduction to Magnetochemistry, Academic Press, 1968.
3. Dutta, R. L.; Syanal, A. Elements of Magneto chemistry, 2nd edition, Affiliated East West Press, 1993.
4. Drago, Russell S. Physical Methods for Chemists, 2nd edition, Saunders College Publishing, 1992.
ORGANIC CHEMISTRY-I
Code: 24CH102
Max Marks: 70
Text Books:
1. March, Jerry Advanced Organic Chemistry: Reactions, Mechanism and Structure, 6th edition, John
Wiley, 2007.
2. Carry, F. A.; Sundberg, R.J. Advanced Organic Chemistry, 3rd edition, Plenum, 1990.
3. Sykes, Peter A Guide Book to mechanism in Organic Chemistry, 6th edition, Longman, 1989.
4. Morrison, R. T.; Boyd, R. N. Organic Chemistry, 6th edition, Prentice Hall, 1992.
5. Kalsi, P. S. Organic Reactions and their Mechanisms, 2nd edition, New Age International Publishers,
2000.
Reference Books:
1. Mukherji, S.M.; Singh, S.P. Reactions Mechanism in Chemistry, Vol. I, II, III, Macmillan, 1985.
2. Nasipuri, D. Stereochemistry of Organic Compounds, 2nd edition New Age International Publishers,
1994.
3. Kalsi, P.S. Stereochemistry of Organic Compounds, 2nd edition, New Age International, 1993.
4. Kalsi, P.S. Stereochemistry: Conformation and Mechanism, 2nd edition, Wiley Eastern Limited, 1993.
PHYSICAL CHEMISTRY-I
Code: 24CH103
Max Marks: 70
Text Books:
1. Atkins, P.W. Physical Chemistry, 3rd edition, ELBS, 1987.
2. Chandra, A.K Introductions to Quantum Chemistry, 4th edition, Tata McGraw Hill, 1994.
3. Young, R-J; Lovell, P.A. Introduction to Polymers, 2nd edition, Replika Press Pvt. Ltd., 1991.
4. Flory, P.J. Principles of Polymer Chemistry, 1st edition, Asian Book Private Ltd., 2006.
5. Crow, D.R. Principles and Applications of Electrochemistry, 4th edition, Chapman and Hall, London,
1994.
Reference Books:
1. Levine, Ira N. Quantum Chemistry, 5th edition, Prentice-Hall International, Inc., 2000.
2. McWeeny, R. Coulson’s Valence, 3rd edition, ELBS, Oxford University Press, 1979.
3. Moore, J.W.; Pearson, R.G. Kinetics and Mechanism, 2nd edition, John Wiley and Sons, 1981.
4. Y. Moroi Micelles: Theoretical and Applied Aspects, 1st edition, Plenum Press, 1992.
5. Bockris, John O’M; Reddy, Amulya K.N. Modern Electro-Chemistry, 2nd edition, Plenum Press, New
York, 1998.
Text Books:
1. 1stSteiner, E. The Chemistry Mathematics, 1st edition, Oxford University Press.
2. 1stDoggett; Sucliffe Mathematics for Chemistry, 1st edition, Longman, 2003.
3. Daniels, F. Mathematical Preparation for Physical Chemistry, McGraw Hill.
4. Hirst, D.M. Chemical Mathematics, Longman.
5. Barrante, J. R. Applied Mathematics for Physical Chemistry, 3rd 2004. edition, Prentice Hall, 2004.
6. Tebbutt Basic Mathematics for Chemists, 1st edition, John Wiley, 1994.
Text Books:
1. Lehninger, A.L. Principles of Biochemistry, Worth Publishers.
2. Stryer, L. Biochemistry, W.H. Freeman
3. Rawn, J. David Biochemistry, Neil Patterson.
4. Voet; Voet Biochemistry, John Wiley.
5. Conn, E.E.; Stumpf, P. K. Outlines of Biochemistry, John Wiley.
Suggested Readings:
1. Hunt, R.; Shelley, J. Computers and Common Sense, Prentice Hall.
2. stNorris, A.C. Computational Chemistry, 1 edition, John Wiley & Sons, 1981.
3. Killingbeck, J.P.; Hilger, Adam Microcomputer Quantum Mechanics.
4. Rajaraman, V. Computer Programming in FORTRAN IV, 4 edition, Prentice Hall India Pvt. Ltd., 1997.
5. Rajaraman, V.; RadhaKrishnan, V. An Introduction to Digital Computer Design, Prentice Hall.
Contents:
1. Viscosity:
(i) Determination of percentage composition of a liquid mixture by viscosity measurement.
(ii) Determination of molecular weight of a high polymer (say polystyrene) by viscosity
measurement.
2. Surface Tension:
(i) Determination of Parachor value of >CH2 group.
(ii) To measure interfacial tension and to test the validity of Antonoff’s rule.
(iii) To compare cleansing power of two detergents.
(iv) To determine the critical micelle concentration of a soap by surface tension method.
3. Solubility:
(i) Determination of solubility of an inorganic salt in water at different temperatures and hence to
draw the solubility curve.
(ii) To study the effect of addition of an electrolyte on the solubility of an organic acid.
(iii) To study the variation of solubility of Ca(OH) 2 in NaOH solution and hence determine the
solubility product.
4. Colloidal State:
(i) To compare the precipitation power of Na +, Ba+2& A1+3 ions for As2S3 sol.
(ii) To study interaction between arsenious sulphide and ferric hydroxide sol.
5. Density: Determine the partial molar volume of ethanol in dil. aqueous solution at room temperature
Theory Paper
Total: 100 Marks
External: 70 Marks
Internal:30 Marks
External: 70 Marks
10 Question (MCQ): 1 mark each (1x10 = 10)
Answer any 6 out of 8 (Very Short 20-30 Words): 2 marks each (2x6 = 12)
Answer any 6 out of 8 (Short 50-70 Words): 3 marks each (3x6 = 18)
Answer any 6 out of 8 (Long 100-120 Words): 5 marks each (5x6 = 30)
Internal: 30 Marks
Two Internal Assessment Examinations will be conducted, each carrying 50 marks. The higher of the two
scores will be considered for the final assessment.
Lab
Practical: 100 Marks
External: 70 Marks
Internal: 30 Marks
External (Two programs): 70 Marks
Program Writing: 10 + 10 Marks
Algorithm& Flowchart: 5 + 5 Marks
Program Execution: 15 + 15 Marks
Viva: 10 Marks
Semester 2
Theory
Course Topic L T P Credit Theory Internal Practical Total
Code Marks Marks Marks Marks
24CH201 Inorganic Chemistry-II 4 0 0 4 70 30 0 100
24CH202 Organic Chemistry-II 4 0 0 4 70 30 0 100
24CH203 Physical Chemistry-II 4 0 0 4 70 30 0 100
24CH204 Group Theory, Spectroscopy 4 0 0 4 70 30 0 100
And Diffraction Methods
Practical
24CH291 Inorganic Chemistry Lab 0 0 4 4 0 30 70 100
24CH292 Organic Chemistry Lab 0 0 4 4 0 30 70 100
24CH293 Physical Chemistry Lab 0 0 4 4 0 30 70 100
Total 28 280 210 210 700
Detailed Syllabus
INORGANIC CHEMISTRY-II
Code: 24CH201
Max. Marks: 70
Suggested Readings:
1. Cotton, F.A.; Wilkinson Advanced Inorganic Chemistry, 6 th edition, John Wiley & Sons, 1999.
2. Huheey, James E. Inorganic Chemistry: Principles of Structure and Reactivity, 4th edition, Harper Collins
College Publishers, 1993.
3. Greenwood, N.N. and Earnshaw, A. Chemistry of the Elements, 2 nd edition, Butterworth Heinemann, A
division of Read Educational & Professional Publishing Ltd., 2001.
4. Lever, A. B. P. Inorganic Electronic Spectroscopy, 2nd edition, Elsevier Science Publishers B.V., 1984.
5. Carlin, Richard L. and Duyneveldt, A. J. Van Magnetic Properties of Transition Metal Compounds,
Inorganic Chemistry Concepts 2, Springer-verlag New York Inc., 1977.
ORGANIC CHEMISTRY-II
Code: 24CH202
Max Marks: 70
UNIT I
Reaction Mechanism, Structure and Reactivity (8 hrs)
Types of mechanism, types of reactions, thermodynamics and kinetic requirement. Kinetic and thermodynamics
control, Hammond’s postulate, Curtin-Hammett Principle, Potential energy diagrams, transition states and
intermediates, method of determining mechanisms, isotope effects.
Addition to Carbon-Carbon Multiple Bonds (7 hrs)
Mechanistic and stereochemical aspects of addition reaction involving electrophiles, nucleophiles and free
radicals, regio and chemoselectivity, orientation and reactivity. Addition to cyclopropane ring. Hydrogenation of
double and triple bonds, hydrogenation of aromatic ring. Hydroboration. Michael reaction. Sharpless asymmetric
epoxidation.
UNIT III
Free Radical Reactions (8 hrs)
Type of free radical reactions, free radical substitution mechanism at an aromatic substrate, neighbouring group
assistance. Reactivity for aliphatic and aromatic substrates at a bridgehead. Reactivity in the attacking radicals.
The effect of solvents on reactivity. Allylic halogenation (NBS), oxidation of aldehydes to carboxylic acids, auto-
oxidation. Coupling of alkynes and arylation of aromatic compounds by diazonium salts. Sandmeyer reaction.
Free Radical Rearrangement. Hunsdiecker reaction.
Elimination Reaction (7 hrs)
The E2, E1 and E1cB mechanisms and their spectrum, Orientation of the double bond. Reactivity effects of
substrate structure, attacking base, the leaving group and the medium. Mechanism and orientation in pyrolytic
elimination.
Suggested Readings:
1. March, Jerry Advanced Organic Chemistry: Reactions, Mechanism and Structure, 6 th edition, John
Wiley, 2007.
2. Carry, F. A.; Sundberg, R.J. Advanced Organic Chemistry, 3rd edition, Plenum, 1990.
3. Sykes, Peter A Guide Book to mechanism in Organic Chemistry, 6th Longman, 1989.
4. Morrison, R. T.; Boyd, R. N. Organic Chemistry, 6 th edition, Prentice Hall, 1992.
5. Kalsi, P. S. Organic Reactions and their Mechanisms, 2nd edition, New Age International Publishers,
2000.
PHYSICAL CHEMISTRY-II
Code: 24CH203
Max Marks: 70
Suggested Readings:
1. Atkins, P.W. Physical Chemistry, 3rd edition, ELBS, 1987.
2. Chandra, A.K Introductions to Quantum Chemistry, 4 th edition, Tata McGraw Hill, 1994.
3. Laidler, Keith J. Chemical Kinetics, 3rd edition, Harper & Row, Publishers, New York.
4. Young, R-J; Lovell, P.A. Introduction to Polymers, 2 nd edition, Replika Press Pvt. Ltd., 1991.
5. Flory, P.J. Principles of Polymer Chemistry, 1st 6th edition, Asian Book Private Ltd., 2006.
6. Crow, D.R. Principles and Applications of Electrochemistry, 4 th and Hall, London, 1994.
Code: 24CH204
Max. Marks: 70
Suggested Readings:
1. Windawi, H.; Ho, F.L. Applied Electron Spectroscopy for Chemical Analysis, Wiley Interscience.
2. Parish, R.V. NMR, NQR, EPR and Mossbauer Spectroscopy in Inorganic Chemistry, 1st edition, Ellis
Harwood, 1990.
3. Drago, Russell S. Physical Methods for Chemists, 2 nd edition, College Publishing, 1992.
4. Cotton, F.A. Chemical Applications of Group Theory, 3 rd edition Science Publication, 1971.
5. Wiley Ghosh, P.K. Introduction to Photoelectron Spectroscopy, 1 st edition Inter Science, 1982.
6. John Wiley Glusker, J.P. Crystal Structure and Analysis: a Primer, Oxford University Press, 1985.
7. Reddy, K.V. Symmetry and Spectroscopy of Molecules, 1st Age International (P) Ltd., 1998.
8. Banwell, C.N. Fundamentals of Molecular Spectroscopy, 4 th edition McGraw-Hill Publishing Company
Ltd., 1994.
Contents:
1. Preparation of hexamminecobalt (III) chloride and determine the percentage of cobalt in the product
iodimetrically.
2. Preparation of chloropentaammine cobalt (III) chloride and interpretation of electronic spectrum and
magnetic properties.
3. Preparations of nitropentamminecobalt (III) chloride from chloropentaamminecobalt (III) chloride and
interpretation of electronic spectrum and magnetic properties.
4. Preparations of nitritopentamminecobalt (III) chloride from chloropentaamminecobalt (III) chloride and
interpretation of electronic spectrum and magnetic properties.
5. Preparation of cis-and trans isomers of [Co(en)2Cl2]Cl and interpretation of electronic spectra and
magnetic properties.
6. Preparations of Cu2(CH3COO)4 (H2O)2 from CuSO4.5H2O and interpretation of electronic spectrum and
magnetic properties.
7. Preparation of cis-and trans isomers of K[Cr(C2O4)(H2O)2].2H2O and interpretation of electronic spectra
and magnetic properties.
8. Preparation of Tris(thiourea)cuprous (I) sulphate [Cu(tu) 3]2SO4.2H2O (Where tu stands for thiourea) and
determine the percentage of copper in the product iodimetrically.
9. Preparation of [Co(acac)3] and interpretation of electronic spectrum and magnetic properties.
10. Preparation of potassium trioxalatoaluminate(III) and tris(acetylacetonato)aluminium(III).
Contents:
1. Quantitative Analysis Separation and identification of organic tests and preparation of their derivatives.
2. Organic Synthesis via two steps preparation
a. p-Nitroanilinefromacetanilide.
b. p-Bromoanilinefromacetanilide
c. Anthranilic acid from phthalic anhydride.
d. p-Bromoacetanilidefromaniline.
e. p-Nitroacetanilidefromaniline.
Theory Paper
Total: 100 Marks
External: 70 Marks
Internal:30 Marks
External: 70 Marks
10 Question (MCQ): 1 mark each (1x10 = 10)
Answer any 6 out of 8 (Very Short 20-30 Words): 2 marks each (2x6 = 12)
Answer any 6 out of 8 (Short 50-70 Words): 3 marks each (3x6 = 18)
Answer any 6 out of 8 (Long 100-120 Words): 5 marks each (5x6 = 30)
Internal: 30 Marks
Two Internal Assessment Examinations will be conducted, each carrying 50 marks. The higher of the two
scores will be considered for the final assessment.
Lab
Practical: 100 Marks
External: 70 Marks
Internal: 30 Marks
External (Two programs): 70 Marks
Program Writing: 10 + 10 Marks
Algorithm& Flowchart: 5 + 5 Marks
Program Execution: 15 + 15 Marks
Viva: 10 Marks