course : chem 401f - rajshahi university web pagedept.ru.ac.bd/chemistry/syllebus/syl_2006_5.doc ·...

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DEPARTMENT OF CHEMISTRY FACULTY OF SCIENCE THE UNIVERSITY OF RAJSHAHI Syllabus for The Degree of Master of Science (M. Sc) in Chemistry Session: 2005-2006 Examination – 2006 PHYSICAL CHEMISTRY BRANCH: Courses Course Title Uni t Cred it Mark s Chem-511F Theoretical Chemistry-III 1.0 4 100 Chem-512F Spectroscopy-II 1.0 4 100 Chem-513F Electrolyte solutions and Electrode Processes 1.0 4 100 Chem-514F Advanced Chemical Kinetics 1.0 4 100 Chem-515F Physical Chemistry of Macromolecules 1.0 4 100 Chem-511AH Class Assessment –V 0.5 2 50 Chem-511VH* Viva-voce–V 0.5 2 50 Chem-511L** Physical Chemistry Practical –V OR 2 8 200 Chem-599*** Thesis / Dissertation on topics of Physical Chemistry * Viva-voce examination includes the assessment of the students through oral examination of all the courses. ** Laboratory courses include 30% (60) marks for continuous Lab. assessment. File: Chem(M)

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Page 1: Course : Chem 401F - Rajshahi University Web Pagedept.ru.ac.bd/chemistry/syllebus/syl_2006_5.doc · Web viewKeith J. Laidler : Chemical Kinetics (3rd. edition) S. Glasstone, K.J

DEPARTMENT OF CHEMISTRYFACULTY OF SCIENCE

THE UNIVERSITY OF RAJSHAHI

Syllabus for The Degree of Master of Science (M. Sc) in

ChemistrySession: 2005-2006

Examination – 2006

PHYSICAL CHEMISTRY BRANCH:Courses Course Title Unit Credit MarksChem-511F Theoretical Chemistry-III 1.0 4 100Chem-512F Spectroscopy-II 1.0 4 100Chem-513F Electrolyte solutions and Electrode

Processes1.0 4 100

Chem-514F Advanced Chemical Kinetics 1.0 4 100Chem-515F Physical Chemistry of Macromolecules 1.0 4 100Chem-511AH Class Assessment –V 0.5 2 50Chem-511VH* Viva-voce–V 0.5 2 50Chem-511L** Physical Chemistry Practical –V OR 2 8 200Chem-599*** Thesis / Dissertation on topics of

Physical Chemistry

* Viva-voce examination includes the assessment of the students through oral examination of all the courses.

** Laboratory courses include 30% (60) marks for continuous Lab. assessment.

** Thesis includes 30% (60) marks for oral examination on the thesis.

Examination of the theory courses of 100 marks (1.0 unit, 4 credit) shall be of 4 (four) hours duration, and of the practical courses of 200 marks (1.0 unit, 4 credit) shall be of 24 (twenty for) hours duration (4 days). 30% marks of the practical courses are assigned for continuous Lab. assessment. The students shall submit a report after each Lab. class to the Lab. teacher(s) for evaluation. (After evaluation the report shall be returned to the students). The lab. teacher(s) shall submit the average marks of all Lab. evaluation in sealed envelopes to the chairman of the relevant examination committee within three weeks from the last lab. held.

The class assessment course include tutorial, terminal, home assignment, and /or class examinations taken on theoretical courses by the relevant course teacher(s) during the academic year. The class teacher(s) of each course shall submit the average consolidated marks of class assessments in sealed envelope to the Chairman of the relevant examination committee within three weeks from the last class held. The examination committee shall send a copy of consolidated marks for each of the viva-voce examination, class assessment, lab. evealuation and practical examinations to the controller of examinations

File: Chem(M) Syl-2005

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* No student shall be allowed to sit for the examination having less than 60% class attendance.

Course : Chem-511FTheoretical Chemistry-III

Examination - 4 HoursFull Marks : 100 (1 unit, 4 credit)

(80 lectures, 4 lectures per week, total 20 weeks )

1. Quantum theory of the chemical bond - diatomic molecules (20 lectures): Born-Oppenheimer approximation; nuclear motion in diatomic molecules; the hydrogen molecule ion (H2

+); approximate treatments of H2+

ground electronic state; molecular orbitals for H2+ excited states; molecular

orbital (MO) configurations of homonuclear diatomic molecules; electronic terms for diatomic molecules; the hydrogen molecule (H2); valence-bond (VB) treatment of H2; comparison of MO and VB theories; MO and VB wave functions for homonuclear diatomic molecules; excited states of H2; electron probability density; dipole moments; the Hartree-Fock method for molecules; self-consistent-field (SCF) wave functions for diatomic molecules; MO and VB treatments of heteronuclear diatomic molecules; the valence electron approximation; configuration iteration (CI) wave functions.

2. Quantum theory of the chemical bond - polyatomic molecules (20 lectures): Ab inito, density-functional, semiempirical and molecular-mechanics methods; electronic terms of polyatomic molecules; the SCF MO treatment of polyatomic molecules; basis functions; the SCF MO treatment of H2O; population analysis; the molecular electrostatic potential and atomic charges; localized MOs; the SCF MO treatment of methane, ethane, and ethylene; molecular geometry.

3. -electron theory of organic molecules (10 lectures): Hückel MO theory; the use of symmetry for determining Hückel orbitals; cyclic conjugated polyolefins and Hückel’s 4n + 2 rule; aromaticity and antiaromaticity; non-classical structures; heteroatomic molecules; the free electron model of -electron molecules.

4. Statistical Mechanics and quantum statistics (20 lectures): Phase space and the Liouville’s theorem; equipartition of energy. Quantum statistics: Boltzmann statistics, Fermi-Dirac and Bose-Einstein statistics, comparison of the three statistics; quantum statistics of weakly degenerate and strongly degenerate ideal Fermi-Dirac gases, an ideal gas of photons (blackbody radiation); the density matrix; the classical limit from quantum mechanical expression for Q. Statistical thermodynamics of crystalline solids:

vibrational spectrum of a monatomic crystal, Einstein and Debye theories of the heat capacity of crystals, lattice dynamics, phonons, and point defects in crystals. Theories of liquids: The theory of significant structures and the Lennard-Jones Devonshire theory.

Books recommended:1. Ira N. Levine : Quantum Chemistry2. J.N. Murrel, S.F.A. Kettle & J.M. Tedder : Valence Theory3. P.W. Atkins : Molecular Quantum Mechanics

(3rd. edn.)4. Donald A. Mc Quarric : Quantum Chemistry 5. H. Eyring, J. Walter & G.E. Kimball : Quantum Chemistry6. R. Anantharaman : Fundamentals of

Quantum Mechanics7. A.K. Chandra : Introductory Quantum

Chemistry8. Donald A. McQuarrie : Physical Chemistry,

A Molecular Approach9. S. Glasstone : Theoretical Chemistry10. Donald A. McQuarrie : Statistical Thermodynamics11. Gurdeep Raj : Advanced Physical Chemistry

-------------------

Course : Chem-512FSpectroscopy-II

Examination - 4 HoursFull Marks : 100 (1 unit, 4 credit)

(80 lectures, 4 lectures per week, total 20 weeks)

1. Raman spectroscopy (20 lectures): Classical and quantum theory; rotational Raman spectrum; instrumentation; effect of nuclear spin; molecules without a centre of symmetry; vibrational Raman spectra; mutual exclusion principles; polarization of Raman lines. Group theoretical analysis of vibrational spectra; vibrational analysis of single crystals; determination of structure by the application of Raman and infrared selection rules; vibrational-rotational Raman spectra; hyper Raman effect.

2. NMR spectroscopy (20 lectures): (a) 13C, 19F, 14N, 15N, 31P NMR spectroscopy. (b) Multiple pulse NMR experiments with some simple applications. (c) Some two-dimensional NMR experiments, CIDNP experiments.

3. Fluorescence spectroscopy (10 lectures): transition probabilities and lifetime, quantum yield, fluorescence intensity and polarization,

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fluorophores and fluorescence probes, fluorescence parameters, molecular dynamics study.

4. Electron spin (paramagnetic) resonance spectroscopy (ESR / EPR) (10 lectures): Introduction; principles; instrumentation; spectrum; hyperfine structure; radicals; anions of aromatic hydrocarbons; relation between hyperline-splitting and unpaired electron density; interpretation of ESR spectra; ESR spectra of transition metal complexes as single crystals; applications.

5. Optical rotatory dispersion (ORD) and circular dichroism (CD) (10 lectures): Optical activity and circularly polarized light; parameters for optical activity; measurement of ORD and CD; physical basis of optical activity; optically active chromophores; the use of CD to determine secondary structures.

6. Mossbauer spectroscopy (10 lectures): Principles; experimental methods; theoretical aspects; quadrupole splitting; magnetic hyperfine interaction; internal magnetic field in molecules; applications.

Books recommended:1. D.A. Skoog : Principles of Instrumental Analysis2. B.P. Straughan & S. Walker : Spectroscopy3. B.K. Sharma : Spectroscopy4. C.N. Banwell : Fundamentals of Molecular Spectroscopy5. P.S. Sindhu : Molecular Spectroscopy6. I.D. Campbell & R.A. Dwek : Biological Spectroscopy7. D. Freifelder : Physical Biochemistry

----------------

Course: Chem-513FElectrolyte solution and Electrode Processes

Examination - 4 HoursFull Marks : 100 (1 unit, 4 credit)

(80 lectures, 4 lectures per week, total 20 weeks)

1. Structure and properties of electrolyte solutions (15 lectures): Structure and properties of water; intermolecular forces; solubilization process; solvation of ions – theories and energetics, determination of solvation number; Debye-Hückel theory of ion-ion interactions in electrolyte solutions, critical appreciation of Debye-Hückel theory; modification of Debye-Hückel theory; activity coefficient and methods for its determination; theory of ion association, ion association equilibrium. Diffusion in electrolyte solutions: Fick’s laws, application of Fick’s laws to

electrolyte solutions, ion-ion interaction during diffusion of electrolytes, diffusion potential.

2. Interfacial electrochemistry (20 lectures): Origin and thermodynamics of electrode potential: potential differences in electrochemical systems, electromotive force and electrode potentials as the sum of Volta potentials, the nature of potential differences across phase boundaries, the Nernst osmotic theory and the hydration theory of electrode potentials. Theories of double layer formation at the electrode-solution interfaces: formation of the double layer; the parallel plate condenser theory (Helmholtz double layer), the diffuse layer theory (Gouy-Chapman double layer), the adsorption theory (Setern’s treatment) of the double layer; recent developments in double layer theory. Adsorption at electrode surfaces: isotherms and the behaviour of reactant ions and molecules at electrodes – Langmuir isotherm, Temkin isotherm and heterogeneity of interaction effects, electrochemical isotherms for ion adsorption.

3. Kinetics of electrode processes (15 lectures): Electrode polarization and overpotential; classification of polarization phenomenon, the concept and theory of diffusion overpotential; diffusion-controlled reactions; principles and applications of polarography; basic factors in ion discharge; formulation of overall kinetic rate equation, concentration dependence of rate of a discharge step, net currents and exchange currents; heats of activation and frequency factors; activation controlled reactions; kinetics and mechanism of some simple electrode reactions, viz., hydrogen evolution at the cathode and oxygen evolution at the anode.

4. Some electrochemical systems of technological importance (10 lectures): Corrosion and passivation of metals, corrosion testing, corrosion industries, theories of corrosion and methods of combating corrosion; electrochemical energy conversion devices, primary and secondary batteries, fuel cells, electroplating of metals, viz., Cu, Ni, and Cr; factors governing the natuer of deposits; ornamental and porous deposits

5. Organic reactions at electrodes (20 lectures): The Electrolysis Cell; choice of working and reference electrodes; selection of solvent and supporting electrolyte. Reduction of functional groups: carbonyl compounds, nitro groups, carbon-halogen bonds, unsaturated compounds, carbon-nitrogen bonds, organosulfur compounds, organometallic compounds, peroxides, reduction of carbon-nitrogen single () bonds. Oxidation of functional groups: the Kolbe reaction, mechanism and role in organic synthesis, oxidation of unsaturated compounds, anodic substitution, alkoxylation, acetoxylation, cyanation and acetamidation; oxidation of aromatic alcohols, anhydrides; oxidation of olefins; anodic halogenation. Electrosynthesis of some compounds of commercial importance: propylene oxide, hydroquinone, adiponitrile, tetraethyl lead etc.

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Books Recommended:1. D. Eisenberg and w. Kauzmann : The Structure and Properties of Water2. J.O’M. Bockris and A.K.N. Reddy : Introduction to Electrochemistry3. B.E. Conway : Electrode Processes4. K.J. Vetter : Electrochemical Kinetics5. G. Khortum : Treatise on Electrochemistry6. L. Anthrpov : Theoretical Electrochemistry7. W. Blum and G.B. Hogaboom : Principles of Electroplating and

Electroforming8. Kohler and Creighton : Electrochemistry –

Principles and Applications9. Mars G. Fontans and Greene : Corrosion Engineering10. S.N. Banerjee : An Introduction to the Science of

Corrosion and Its Inhibition11. E. C. Potter : Electrochemistry –

Principles and Applications12. G. Mantell : Industrial Electrochemistry13. M.R. Rifi and Frank H. Covitz : Introduction to Organic

Electrochemistry14. Demetrios K. Kyriacou : Basics of Electro-organic Synthesis

----------------

Course : Chem-514FAdvanced Chemical Kinetics

Examination - 4 HoursFull Marks : 100 (1 unit, 4 credit)

(80 lectures, 4 lectures per week, total 20 weeks)

1. Energy of activation (20 lectures): Statistical distribution of molecular energies: simple statistical expressions; Tolman’s theorem. Potential energy surfaces: ab initio calculations of potential energy surfaces: treatments based on London equation, variational calculations; semiempirical calculations of potential energy surfaces: London-Eyring-Polanyi (LEP) method, Sato method, modified LEP methods, bond-energy-bond-order (BEBO) method; empirical treatments of activation energy.

2. Theories of Reaction rates (10 lectures): Conventional transition state theory (STST); derivations of rate equation from CTST; symmetry numbers and statistical factors; applications of CTST to reaction between atoms and reactions between molecules with a few specific examples (e.g., the reaction

H + HBr = H2 + Br2); thermodynamic formulation of CTST; assumptions and limitations of CTST; multiple crossing and the equilibrium hypothesis; reparability of the reaction co-ordinate; quantum effects; extensions of transition state theory; variational transitional-state theory; quantum-mechanical transition-state theory; microscopic reversibility and detailed balance.

3. Theory of unimolecular reactions (10 lectures): Recapitulation of Lindemann-Christiansen and Hinshelwood’s treatments. The Rice-Ramsperger-Kassel (RRK) treatment, Slater’s treatment, Marcus’s extension of RRK treatment (RRKM); influences of foreign gases; intramolecular and intermolecular energy transfer; laser-induced unimolecular reactions; decomposition of ions; combination and disproportionation reactions; mechanism of atom and radical combinations.

4. Elementary reactions in solution (20 lectures): Effects of solvents on reaction rates; factors determining reaction rates in solution; collision theory in solutions; transition-state theory for reactions in solution: influence of internal pressure of the solvent, influence of solvation of reactants and activated complex; reaction between ions: influence of solvent dielectric constant on rates, pre-exponential factors of ionic reactions, single-sphere activated complex for activated complex, influence of ionic strength, more advanced treatments for ionic reactions in solutions; ion-dipole and dipole-dipole reactions in solutions; influence of hydrostatic pressure on rates; substituent and correlation effects on rates; diffusion controlled reactions: full microscopic diffusion control and partial microscopic diffusion control, reactions involving two ions.

5. Composite reactions (10 lectures): Rate equations for composite mechanisms: simultaneous and consecutive reactions, rate-determining steps, microscopic reversibility and detailed balance; chain reactions; some inorganic reaction mechanisms: hydrogen-bromine reaction, hydrogen-chlorine reaction, hydrogen-iodine reaction, comparison of hydrogen-halogen reactions formation and decomposition of phosgene, decomposition of nitrogen pentoxide, decomposition of ozone, para-ortho hydrogen conversion; mechanism of organic decomposition reactions: Goldfinger-Letort-Niclause rules, molecular processes, decomposition of ethane and acetaldehyde, inhibition mechanisms; mechanism of gas-phase combustion of hydrogen and hydrocarbons.

6. Reaction dynamics (10 lectures): importance of reaction dynamics; molecular-dynamical calculations of chemical reactions: the reaction H + H2, the reaction Br + H2 and more complex reactions; chemiluminesence;

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features of potential energy surfaces: attractive surfaces for exothermic reactions, repulsive surfaces for exothermic reactions, surfaces of intermediate types for exothermic reactions, selective enhancement of reaction, disposal of excess energy, gradual and sudden surfaces, influence of rotational energy; molecular beams: stripping and rebound mechanisms, state-to-state kinetics.

Books Recommended:1. P. W. Atkins : Physical Chemistry (7th edition)2. Keith J. Laidler : Chemical Kinetics (3rd. edition)3. S. Glasstone, K.J. Laidler & H. Eyring : The Theory of Rate Processes4. K.J. Laidler and J.H. Meiser : Physical Chemistry

--------------------------

Course : Chem-515FPhysical Chemistry of Macromolecules

Examination - 4 hoursFull marks : 100 (1 unit, 4 credit)

80 lectures, 4 lectures per week, total 20 weeks

1. Introduction to macromolecules: (13 lectures): The macromolecular concept; some basic terms and definitions: monomer, oligomer and polymer; repeating unit; end groups; degree of polymerization. Polymer molecular weights and distributions and their determination: osmotic pressure measurements (Mn), Light scattering measurements (Mw), sedimentation velocity and sedimentation equilibrium methods (Mz), viscosity and molecular weight (Mv); natural and synthetic polymers; polymerization and functionality principle; linear, branched and cross-linked (network) polymers; thermoplastics and thermosets; elastomers, fibres and plastics; copolymers; polymer nomenclature; isomerism in polymers: positional, stereo and geometrical isomerism.

2. Condensation or step-growth polymerization (10 lectures): Various types of condensation polymers: polyesters, polyamides, polyurethanes, polycarbonates, polyethers, and inorganic polymers. Kinetics of linear condensation polymerization; relation between average functionality, extent of reaction, and degree of polymerizatin: Carothers’ equation; bifunctional systems; molecular weight distribution in linear condensation polymerization; factors influencing maximum attainable molecular weight.

3. Addition polymerization (15 lectures): Comparison between step-growth and addition polymerization processes; addition polymerization: free radical, cataionic and anionic; monomers and initiators; effect of

substituents on the polymerization mechanism of vinyl polymers;n. Overall scheme of a free radical polymerization process: methods of radical production, efficiency of initiators, chain propagation, transfer and termination. Kinetics of free radical polymerization, kinetic chain length and average degree of polymerization; chain tansfer and incorporation of its effects in ideal polymerization model; chain transfer constants; inhibition and retardation; deviations from ideal kinetics.

4. Chain growth copolymerization (10 lectures): Coplymerization models; copolymer composition equation from simple (terminal) copolymerization model; characteristics of monomer reactivity ratios; random copolymers, alernating copolymers, formation of long sequences of one monomer unit; azeotropic copolymerizatios; average composition of binary copolymers. Determination of reactivity ratios. Reactivities of monomers and radicals: resonance effects, polar effects and steric effects; the Q–e scheme, rates of free radical copolymerization.

5. Biomacromolecules (10 lectures): Building-block molecules of bio-molecules and their nature; simple ideas of structure and functions of proteins / enzymes, lipids, carbohydrates, and DNA / RNA. Stabilizing forces in biological macromolecules; native and denatured forms of proteins.

6. Specificity and modifications of proteins / enzymes (5 lectures): Trypsin; chymotrypsin; elastage; carboxypeptidase; aminopeptidase; cyanogen bromide cleavage; chemical modification of SH, -S-S-, NH2, imidazole and –S-CH3 groups of proteins.

7. Isolation and purification methodology of proteins / enzymes (5 lectures): Chemistry of solubilization, precipitation and chromatographic separation of proteins.

8. Characterization of proteins (12 lectures): Gel filtration (gel permeation chromatography, GPC); Electrophoresis; 2D peptide mapping; N and C-terminal analysis; aminoacid analysis and degradation of proteins. Enzyme nomenclature; cofactor; enzyme catalyzed reactions having one substrate; Michaelis-Menten approach to enzyme kinetics; Km and Vm

values and their determination; enzymatic assay.

Recommended Books:1. Alfred Rudin : The elements of Polymer Science and Technology 2. George Odian : Principles of Polymerization3. Premamoy Ghosh : Polymer Science and Technology of

Plastics and Rubbers4. Paul C. Hiemenz : Polymer Chemistry the Basic Concepts5. P.J. Flory : Principles of Polymer Chemistry

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6. A. W. Lehninger : Principles of Biochemistry7. R.C. Bohinski : Modern Concepts of Biochemistry8. G. Zubay : Biochemistry9. D. Freifelder : Physical Biochemistry10. R.K. Scopes : Protein Purification11. C.N. Price & R.A. Dwek : Principles and Problems in Physical

Chemistry for Biochemists.Course : Chem-511L

(Physical Chemistry Practical)Examination - 24 (Twenty four) hours (4 days)

Full Marks: 200 (2 unit, 8 credit) Experiment-140, continuos Lab. assessment-60

[N.B. In addition to the experiments listed below more experiments on physical chemistry may be done subject to the availability of the Lab. facilities.]1. Determination of the molar mass of a given polymer. 2. Determination of the limit of homogeneous phase in the three

component system: chloroform-acetic acid-water.3. Determination of the rate constant and order of S2O8

2- in the reaction S2O8

2-(aq)+29-

(aq) 2SO42- +92(S)

4. Kinetic studies on the oxidation of ethanedioic acid.5. Determination of the Avogadro constant.6. Studies on the substituent effect on reactivity by measuring the rate of

base catalysed hydrolysis of methyl benzoate.7. Determination of the G°, S°, H° & Cp° for the equlibrium

reaction I2 + I- I3-.

8. Determination of the energy of activation for the reaction 5 KBr + KBrO3 + 2H2SO4 = 3Br2 +3K2SO4 + 3H2O.

9. Studies of adsorption on liquid surfaces by surface tension measurements.

10. Verification of the formula of inorganic big molecules, e.g., KMnO4 , K2Cr2O7 by the ebullioscopic / Cryoscopic methods.

11. Determination of percentage composition of a binary mixture of nonvolatile nonelectrolyte, e.g., urea, glucose by ebullioscopic / Cryoscopic methods.

12. Determination of Vant Hoff factor of an electrolyte by ebullioscopic / Cryoscopic methods.

13. Determination of the dissociation constant of a weak acid (e.g. acetic acid, oxalic acid etc.) near 100°C/0°C by ebullioscopic / Cryoscopic methods and estimation of pH of the solution.

14. Determination of the hydrolysis constant of a salt conductometrically.15. Determination of activity coefficient conductometrically.16. Kinetic studies on the saponification of an ester conductometrically.17. Determination of the solubility product constant of a suitable salt

conductometrically.18. Determination of the standard oxidation –reduction potential of the

Fe2+/Fe3+ system.19. Determination of the instability constant of the argentamine complex

potentiometrically.20. Determination of the hydrolysis constant of a salt potentiometrically.21. Determination of the mean activity coefficient of an electrolyte

potentiometrically.22. Determination of the equilibrium constant of Sn4+ + 2 Fe2+

Sn2+ + 2 Fe3+ potentiometrically.23. Potentiometric titration of a dibasic acid with NaOH and determination

of the first and second dissociation constant of the acid.24. Determination of Isobestic point.25. Determination of the indicator constant of an indicator.26. Study of the equlibrium in aqueous solution between ferric nitrate and

sodium thiocyanate spectrophotometrically and estimation of stability constant and coordination number of Fe3+.

27. Determination of the solubility product constant of Cu(II) Iodate spectrophotometrically.

Recommended Books:1. D.P. Shoemaker et al : Experiment in Physical Chemistry2. G.S. Weiss et al : Experiments in General Chemistry3 A. Findlay : Practical Physical Chemistry4. R.C. Das : Experimental Physical Chemistry5. J.N. Gurtu : Advanced Experimental Chemistry6. K.K. Sharma : An Introduction of Practical Chemistry7. J.C. Muhler et al : Introduction to Experimental Chemistry8. J. Rose : A Textbook of Practical Physical Chemistry9. J.B. Yadav : Advanced Practical Physical Chemistry10. Newcomb, Wilson et al : Experiments in Physical Chemistry11. Daniels et al : Practical Physical Chemistry12. Brennan et al : Experiments in Physical Chemistry13. S.R. Palit : Practical Physical Chemistry

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14. C.D. Hodgman et al : Handbook of Chemistry and Physics15. R.C. West et al : CRC Handbook of Physics and Chemistry16. L.A. Lange : Handbook of Chemistry

ORGANIC CHEMISTRY:Courses Course Title Units Credits Marks

Chem-521F Methods and Synthesis 1.0 4 100Chem-522F Synthetic Organic Chemistry &

Biomolecules1.0 4 100

Chem-523F Advanced Organic Spectroscopy 1.0 4 100Chem-524F Industrial and Polymer Chemistry 1.0 4 100Chem-525F* Stereochemistry and conformations 1.0 4 100Chem-526F* Advanced Organic Reactions 1.0 4 100Chem-527F* Bioorganic Chemistry 1.0 4 100Chem-521AH Class Assessment –V 0.5 2 50Chem-521VH Viva-voce–V 0.5 2 50Chem-521L** Organic Chemistry Practical –V OR 2 8 200Chem-599*** Thesis –I (Organic / Industrial)

* Any one course shall be chosen out of the three optional courses subject to the approval of the branch. ** Laboratory courses include 30% (60) marks for continuous Lab. assessment.*** Thesis includes 30% (60) marks for oral examination on the thesis.

Examination of the theory courses of 100 marks (1.0 unit, 4 credit) shall be of 4 (four) hours duration, of 50 marks (0.5 unit, 2 credit of 2 (two) hours duration and of the practical of 100 marks (1.0 unit, 4 credit) shall be of 12 (twelve) hours duration (2 days). 30% marks of the practical courses are assigned for continuous Lab. assessment. The students shall submit a report after each Lab. class to the Lab. teacher(s) for evaluation. After evaluation the report shall be returned to the students. The Lab. teacher(s) shall submit the average marks of all Lab. evaluation in sealed envelopes to the chairman of the relevant examination committee within three weeks from the last Lab. class held.

Class assessment course includes tutorial, terminal, home assignment, and /or class examinations taken on theoretical courses by the relevant course teacher(s) during the academic year. Class assessment comprises (a) 80% marks in tutorial, terminal home assignment and /or class examinations and (b) 20% marks for attendance in the class. The class teacher(s) of each course shall submit the average consolidated marks of class assessments and attendance in sealed envelope to the Chairman of the relevant examination committee within three weeks from the last class held.

Viva-voce examination includes the assessment of the students through oral examination of all the courses. No student shall be allowed to sit for the examination having less than 60% class attendance.

Course : Chem-521F(Organic reactions and stereochemistry)

Examination – 4 hoursFull Marks : 100

(80 Lectures; 1 Unit; 4 Credit)

1. Purification and important uses of some solvents & reagents (20 Lectures): Methanol and ethanol, acetone, N,N dimethyl formamide (DMF), dimethyl sulfoxide (DMSO), acetone, chloroform, dichloro methane, benzene, ether, tetrahydorfuran, (THF) toluene, diethylene glycol (DEG) BBr3, BF3 (etherate), AlCl3, dicyclohexyl carbodiimide (DCC), Girad reagents, perbenzoic and periodic acids, N-bromosuccinimide (NBS) polyphosphoric acid (PPA) trifluoroacetic acid (TFAA), trimethyl silyl chloride (TMS), Raney nickel, Köser’s reagents, Dess Martin reagents tri- Köser’s reagents, triisobutyl tin hydride, thulliam trinitrate (TTN).

2. Redox reactions :

a) Oxidation reactions (10 Lectures): Oxidation of alcohols with Cr(VI) with DMSO and DCC, oxidation with PCC, with Jone’s reagent, Collin’s reagent. Allylic oxidation (SeO2 and Pb(OAc)4). Peracid and periodate oxidation. Lemieux oxidation, Prevost and Woodward oxidation.

b) Reduction reactions (10 Lectures): Catalytic hydrogenation, metal hydride reductions, [LiAlH4, LiAlH(OC4H9)3], B2H6, DIBAL, Na-cyanoborohydirde, reduction with dissolving metals, Birch reduction.

3. Alkylation of active methylene compounds (10 Lectures):): The formation of enols and enolate anion and their importance, alkylation of relatively active methylene compounds (C-alkylation and O-alkylation), alkylation of 1,3-dicarbonyl compounds, alkylation of ketones, the formation and alkylation of enamines.

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4. Interconversion and protection of functional groups (15 Lectures):): Hydroxyl (alcoholic and phenolic), carbonyl, carboxyl, amino and thiol groups.

5. Stereochemistry and Conformations (15 Lectures): Stereochemistry, optical activity and chirality, cis-trans isomerism, conformational analysis, strains, methods of correlation for configurations, ORD, CD, etc. Conformation and stereochemistry of cholesterol, cholestane etc.

Recommended Books:1. Adams et.al. (ed.) : Organic Reactions (all volumes)2. H.O. House : Synthetic Application of Organic Reactions3. Carruthers : Some Modern Methods of

Organic Synthesis4. H. Gilman : Advanced Organic Chemistry, (Vol-1 to IV)5. L.F. Fieser and M. Fieser : Topics in Organic Chemistry6. I.L. Finar : Organic Chemistry Vol. 27. R.KJ. Mackil & D.M. Smith : A Guidebook to Organic Synthesis8. P. Simpson : Organometallic Chemistry of the Main

Group Elements9. T.W. Green : Protective Groups in Organic Synthesis.

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Course: Chem 522F(Synthetic Organic Chemistry)

Examination - 4 hoursFull Marks : 100

(80 Lectures, 1 Unit, 4 Credit)

1. Multinuclear aromatic heterocycles (15 Lectures): General nature, preparation and properties; Benzo-derivatives of furan, pyrrole and thiophene; acridine, phenathridine and diazanaphthalenes.

2. Polycyclic aromatic compounds (10 lectures): General nature, structure, reactions and synthesis of annulenes, rotanes, twist compounds, prism compounds, propellanes,cyclophanes, crownethers.

3. Organometallic Chemistry (20 Lectures): Alkyl metal compounds of alkali group, organo-copper compounds, organo-zinc compounds, organo-palladium compounds, organo-silicon compounds, organomagnesim and organoselenium compounds, preparation, properties and synthetic uses.

4. Designing organic synthesis (15 Lectures): Designing organic synthesis involving one step disconnections: disconnection of simple alcohols, olefins and ketones. Two group disconnections: -Hydroxy carbonyl

compounds, , -unsaturated carbonyl compounds and 1,3-dicarbonyl compounds.

5. Synthesis of (20 Lectures):a) Agrochemicals:

i) Herbicides : Vegadex, Avadex, Eptam and Carbyne ii) Fungicides : Vapam, Nabam and Zineb iii) Insecticides : Sevin and Furadam iv) Pyrifenox : 4-(dichloro metheylene)-2-[N-(ά-methyl benzyl )]-

imino-1,2-dithiolane.

b) Some important drugs: Salbutamol, trimethoprime, indomethacin, acetazolamide, naproxen and tolmetin sodium.

Recommended Books:1. E.S. Gould : Mechanism and Structure in

Organic Chemistry2. R.T. Morison & R.N. Boyd : Organic Chemistry3. S. Warren : Disconnection Approach.4. P. Simpson : Organometallic Chemistry of the Main

Group Elements.5. A. Kar : Medicinal Chemistry 6. A. Burger : Medicinal Chemistry vol. I & II

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Course: Chem-523F (Advanced Organic Spectroscopy)

Examination - 4 hoursFull Marks : 100

(80 Lectures; 1 Unit; 4 Credit)

1. NMR Spectroscopy (20 Lectures): 1H, 13C, 31P, 19F NMR spectroscopy: preamble, principles of NMR, situation for other Nuclei, continuous wave and pulsed NMR experiments, FID & processing FID, relaxation, chemical shifts and factors influencing it, origin of coupling, long-range coupling, coupling constant, Signal-to-Noise ratio (SNR), integration of signals, NOE, DEPT, APT; 2D NMR: basic of 2D NMR, general experimental scheme for 2D NMR, COSY, SECSY etc.; Extensive application of NMR to organic molecules.

2. UV- VIS (20 Lectures): Definition of some simple terms: hyperchromic and hypochromic effect, bathochromic and hypsochromic effect, chromophore; conjugation and wavelength shifting; solvent effect on UV-Vissble spectroscopy; Woodward, Woodward-Fieser and Nielsen’s rules for the determination of max to different organic molecules; structural study of simple and complex organic compounds and application to macromolecules, qualitative and quantitative uses.

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3. IR and RAMAN (20 Lectures): IR: Mode of vibration, overtone, combination and difference bands in IR spectroscopy; influencing factors of force constant, approach towards the analysis of an IR spectra; structural study of simple and complex organic compounds and application to macromolecules, qualitative and quantitative uses. Raman: Raman techniques, stocks and anti-stocks lines, utility to organic molecules.

4. MS: GC-MS, LC-MS etc (20 Lectures): MS: Base peak, molecular ion peak, metastable peak and their utility, fragmentation patterns to various organic molecules, description of LIMA, SIMS and FAB techniques in Mass spectroscopy; structural study of simple and complex organic compounds and application to macromolecules. GC-MS, LC-MS: principle and instrumentation of GC and LC; combined techniques (GC-MS, LC-MS) for chemical analyses.

Recommended Books:1. P.S. Sindhu : Molecular Spectroscopy2. J.D. Graybeal : Molecular Spectroscopy3. R.K. Harris : Nuclear Magnetic Resonance

Spectroscopy4. D.L. Pavia, G.M. Lampman : Introduction to Spectroscopy

and G.S.C. Kriz5. Y.R. Sharma : Elementary Organic Spectroscopy6. H.Gunther : NMR Spectroscopy7. J.K.M. Sanders and B.K. Hunter : Modern NMR Spectroscopy8. R.J. Abraham and P. Loftus : Proton and Carbon-13 NMR

Spectroscopy9. E.A.V. Ebsworth, D.W.H. Roukin & : Structural Methods in

S. Croadock Inorganic Chemistry10. I.D. Campbell and R.A. Dwek : Biological Spectroscopy.

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Course: Chem-524F(Industrial and Polymer Chemistry)

Examination - 4 hoursFull Marks : 100

(80 Lectures, 1 Unit, 4 Credit)

1. Petrochemicals (15 Lectures): Definition, chemistry & technology of the production of glycerin and chloroderivatives, detergents, hydrocarbon and chemical solvents: SBP, white spirit, alcohols; the oxoprocesses, future prospect of petrochemicals.

2. Coal (10 Lectures): Origin, classification, coke oven gas; the cooking processes, high and low temperature carbonization processes. Analysis of coal; sampling, proximate and ultimate analysis, calorific value and ignition point.

3. Fermentation and enzymes (7 Lectures): Conditions for fermentation, enzymes and their actions; production of industrial alcohol, purification, by-product, production of absolute alcohol.

4. Fibers and dying (8 Lectures): Fibers: Natural and synthetic fibers (cotton, silk, wool, jute, polyamides and polyesters); Dyeing: classification of dyes based on chemical constitution and application; factors effect the method of applying dye; basic operation of dyeing; techniques of dyeing.

5. General idea on polymer (10 Lectures): Introduction: idea of repeating units, structure of polymers, classification of polymers, intermolecular forces, biological and industrial importance of polymers, end group analysis, polymer solutions: thermodynamics of polymer dissolution, size and shape of macromolecules in solution.

6. Types and mechanism of polymerization (20 Lectures): Polymerization techniques: bulk, solution, suspension, emulsion and gas phase polymerization; types of polymerization reaction: chain polymerization (free radical, ionic, coordination) step polymerizations (poly-condensation, poly-addition, ring-opening); co-polymerization: copolymer composition, monomer reactivity ratio; mechanism of each polymerization reaction; dead and active polymers; microstructure of polymer: linear, branched, cross-linked and stereo-regular polymers & random, alternating, block and graft copolymers, tacticity of polymer (iso-, syn-, atactic).

7. Polymer colloids (10 Lectures): Definition, latex, chemistry of polymer colloid formation, strategies for imparting colloidal stability, application of polymer colloids.

Recommended Books:1. Royal Dutch (shell company) : The Petroleum Handbook2. Nelson : Petroleum Refining Engineering3. Lawry : Chemistry for Coal Utilization.4. R.N. Shreve : Chemical Process Industries5. B. K. Sharma : Industrial Chemistry7. V.R. Gowariker et.al. : Polymer Science8. George Odian : Principles of Polymerization1. Fred W. Bill Maeyer : A Textbook of Polymer Science2. Robert M. Fitch : Polymer Colloids: A Comprehensive

Introduction

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Course: Chem-525F(Stereochemistry and Conformations)

Examination - 4 hoursFull Marks : 100

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(80 Lectures, 1 Unit, 4 Credit)

1. Conformations of heterocyclic rings (15 Lectures): Six-membered ring with one heteroatom; conformation of cholesterols, cholestenone etc.

2. Stereochemistry of macromolecules (10 Lecturer): Stereochemistry and stereo chemical control of polymerization by Zieglar Natta catalysts especially in polymerization of propylene, butadiene, isoprene etc.

3. Asymmetric synthesis using chiral reagents and achiral substrates (15 Lectures): Hydrogen transfer from chiral reducing agents; use of asymmetric MPV reduction to determine the configuration of biphenyl derivatives; use of asymmetric Grignard reagents in creating chiral centers with stereoselectively.

4. The chemistry of organo transition-metal compounds (20 Lectures): -Organotitanium compounds, the Tebbe reagent,. Acyl-iron complexes in enantioselective synthesis and in ketone synthesis, alkyne-cobalt complex, Pauson-Khand reaction in the synthesis of enones, telomerization from conjugated dienes; chromium (Cr)-arene complexes and its synthetic importance.

5. Stereochemistry of steroids (12 Lectures): Configuration of nucleus and substituent groups; conformational analysis of steroids.

6. Stereochemistry of bi-cyclic systems (8 Lectures): 5-3, 5-4, 5-5 (vit. biotin) and 6-6 (decalin) combinations.

Recommended Books:1. Adams et.al. (ed.) : Organic Reactions (all volumes)2. H.O. House : Synthetic Application of

Organic Reactions3. Carruthers : Some Modern Methods of

Organic Synthesis4. H. Gilman : Advanced Organic Chemistry, (Vol-1 to IV)5. L.F. Fieser and M. Fieser : Topics in Organic Chemistry6. L.L. Finar : Organic Chemistry Vol. 27. R.KJ. Mackil and D.M. Smith : A Guidebook to Organic Synthesis8. P. Simpson : Organometallic Chemistry of the

Main Group Elements9. T.W. Green : Protective Groups in Organic Synthesis10. R.O.C. Norman & J.M. Coxon : Principles of Organic Synthesis.

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Course: Chem-526F(Advanced Organic Reactions)

Examination - 4 hoursFull Marks : 100

(80 Lectures, 1 Unit, 4 Credit)

1. Reaction mechanisms and methods of determining them (20 Lectures): Types of mechanisms, type and reactions, kinetic and thermodynamic requirements for reactions, Hammond postulate, microscopic labeling, stereochemical, kinetic evidence, isotopic effects, the effects of molecular structure and environment on reaction rates in terms of reaction and transition states, topic includes theories of reaction rates, reactive intermediates, methods of elucidating reaction pathways, linear free energy relationships and solvent, acid-base, salt and kinetic hydrogen isotope effects. Application to selected reaction pathways.

2. Effects of structure on reactivity (10 Lectures): Resonance and field effects, steric effects, quantitative treatments of the effect of structure reactivity, Hammett equations, Taft equation.

3. Aliphatic and aromatic nucleophilic substitutions (15 Lectures): Neighboring group participation, non-classical carbocation, nucleophilic substitution at allylic carbon, aliphatic trigonal carbon, vinylic carbon, reaction medium phase transfer catalysis, aimbident nucleophile, regioselectivity, ambident substrates, reactive oxygen, sulfur, nitrogen and carbon nucleophiles.

4. Free radical Reaction (15 Lectures): Stability and structure, generation and fate of free radicals, free radical mechanisms in general: substitution mechanism, mechanism at aromatic substrate, neighboring-group assistance in free radical reactions, reactivity for aliphatic substrates, reactivity at a bridgehead position, reactivity in aromatic substrates, reactivity in the attacking radical, effect of solvent on reactivity. Examples of free radical reactions: (i) hydrogen as leaving group; (ii) allylic halogenation; (iii) halogenation of aldehydes; (iv) substitution by oxygen; (v) hydroxylation at an aromatic carbon and other free radical substitution effected by oxygen.

5. Photochemistry (10 Lectures) : Fluorescence, phosphorescence, singlet and triplet states; photosensitization reactions. Examples of photochemical reactions: (i) reactions involving conjugated and non-conjugated/isolated olefinic double bonds; (ii) photorearrangement; (iii) photoaddition; (iv) photosubstitution; (v) valence tautomerization; (vi) photooxidation/ photoreduction; (vii) photocyclization; (viii) photoelimination and extrusion; (ix) photochemistry of aromatic compounds; (x) Norrish I and II type reactions.

6. Electrochemistry (10 Lectures): Principles of electrochemistry, cell parameters; electrochemical reactions: electroreduction of haloalkanes,

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aldehydes, ketones, nitrocompounds, conjugated compounds, Electrooxidation: Electrooxidation of conboxylic acid salts, and some aromatic compounds.

Recommended Books:1. Adams et.al. (ed.) : Organic Reactions (all volumes)2. H.O. House : Synthetic Application of Organic Reactions3. Carruthers : Some Modern Methods of Organic Synthesis4. H. Gilman : Advanced Organic Chemistry, (Vol-1 to IV)5. L.F. Fieser and M. Fieser : Topics in Organic Chemistry6. P. Simpson : Organometallic Chemistry of the

Main Group Elements7. T.W. Green : Protective Groups in Organic Synthesis

Course: Chem-527F(Bioorganic and Food Chemistry)

Examination - 4 hoursFull Marks : 100

(80 Lectures, 1 Unit, 4 Credit)

1. Enzyme-catalyzed reactions (20 Lectures): Definition of enzyme, coenzyme and apoenzyme properties, enzyme inhibitors, origin of enzyme specificity, enzyme-catalyzed interconversion of acetaldehyde and ethanol, ester and carboxylic acid. Enzyme catalyzed SN2 reaction in system living system, transamination reaction to an imine. Enzyme catalyzed Aldol & Claisen condensation reaction, Acyl transfer reaction in living system.

2. Molecular Recognition (15 Lectures): Nucleic acid and some biological catalysts; introduction, recognition of guests by synthetic hosts, natural hosts, ionophores; molecular recognition by an enzyme, catalytically active antibodies, nucleic acids, cryptands, spherands, epitope and antigen.

3. Biomolecules (15 Lectures): Occurrence, structure, stereochemistry and biological properties of lipids, prostaglandins and nucleic acids; biosynthesis of prostaglandins (e.g., PGI), nucleosides (e.g., adenosine, thymidine etc.), nucleotides and nucleic acids (e.g., RNA, DNA).

4. Food, food additives and preservation (5 Lectures): Different classes of foods; types of food additives (polysorbate 60, dimethyl pyrocarbonate ), direct and indirect effect of food additives on health; chemical changes in food during storage at room temperature and at frozen state.

5. Food adulteration (10 Lectures): Definition of adulterated food, common adulterants in different foods; contamination of foods with toxic chemicals, pesticides and insecticides; bacterial and fungal contamination of food.

6. Nutritional aspects of foods (15 Lectures): Function of fats, phospholipids and cholesterol, essential fatty acid deficiency in human beings, effect of excess essential fatty acids, fatty liver and lipotropism, dietary lipids and their relation to the causation of atherosclerosis and ischaemic heart disease; protein efficiency ratio (PER), digestibility coefficient, biological values of protein, net protein utilization (NPU), net protein ratio (NPR), effect of amino acid imbalance and amino acid toxicity.

Recommended Books:1. Seyhan Ege : Organic Chemistry Structure & Reactivity.2. R.K. Bakiaski : Modern Biochemistry3. Harper : Biochemistry4. M. Swaminathan : Advanced Text book on Food and Nutrition, vol. I & II

----------------Course: Chem-521L

(Organic Chemistry Practical)Examination : 24 hours

Marks-200(2 Unit, 8 Credit)

(i) Experiment: 140 marks (ii) Continuous Class Evaluation and class records: 60 marks

1. Crystallization, extraction, distillation and drying of organic compounds / reagents.

2. Fractional distillation: ethanol from sugar; extraction from solution.

3. Multistep organic synthesis: a) synthesis of nitrophenols, paracetamol; b) preparation of sulphanilamide and other sulphur drugs; c) synthesis of benzyllic acid from benzoin via benzil formation; d) preparation of acridone from anthranilic acids; e) methyl orange and salicylic acid from aspirin (some other synthesis may also be included if facilities are made available).

4. Preparation of ketals, esters: fats and detergents; reactions of aldehydes and ketones and heterocyclic compounds like coumarins, beta keto esters, cyclohexene from cyclohexanol

5. Chromatographic method - TLC, column chromatography, paper chromatography.

6. Assay of drugs and raw materials: a) ephedrine hydrochloride;c) penicillin/ ampicilline capsule; d) cotrimoxazole tablet /syrup; e) aspirin tablet etc. (some other suitable compounds if they are available. Use of UV-Vis and IR spectrometers.

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7. Resolution of recemic compounds (acids/bases).

8. Oxidation: selective oxidation; oxidation of primary and secondary alcohol and aldehyde.

9. Reduction: sodium borohydride reduction of benzil and other compounds containing carbonyl groups.

10. Hydroboration: hydroboration of unsaturated hydrocarbons.

11. Phase Transfer Catalysis: Use of PTC in different types of reactions.

12. Reaction kinetics: hydrolysis of tert-butyl chloride etc.

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Course: Chem-599(Organic/Industrial Chemistry Thesis)

Marks-200(2 Unit, 8 Credit)

(i) Thesis submission: 140 marks (ii) Thesis defense: 60 marks

INORGANIC CHEMISTRY:Courses Course Title Unit Credit MarksChem-531F Organometallic Chemistry 1.0 4 100Chem-532F Bio-inorganic Chemistry 1.0 4 100Chem-533F Inorganic Materials 1.0 4 100Chem-534F Analytical Chemistry 1.0 4 100Chem-535H Homogeneous & Heterogeneous

Catalysis0.5 2 50

Chem-536H Environmental Chemistry 0.5 2 50Chem-531AH Class Assessment 0.5 2 50Chem-531VH Viva-voce 0.5 2 50Chem-531L* Inorganic Chemistry Practical & Project

OR 2 8 200

Chem-599** Thesis / Dissertation on topics of Inorganic Chemistry

* Laboratory courses include 30% (60) marks for continuous Lab. assessment.

** Thesis includes 30% (60) marks for oral examination on the thesis.

Examination of the theory courses of 100 marks (1.0 unit, 4 credit) shall be of 4 (four) hours duration, of 50 marks (0.5 unit, 2 credit) of 2 (two) hours duration and of the practical courses of 100 marks (1.0 unit, 4 credit) shall be of 12 (twelve) hours duration (2 days). 30% marks of the practical courses are assigned for continuous Lab. assessment. The students shall submit a report after each lab. class to the lab. teacher(s) for evaluation. After evaluation the report shall be returned to the students. The lab. teacher(s) shall submit the average marks of all lab. evaluation in sealed envelopes to the chairman of the relevant examination committee within three weeks from the last Lab. held.

Class assessment course includes tutorial, terminal, home assignment, and /or class examinations taken on theoretical courses by the relevant course teacher(s) during the academic year. Class assessment comprises (a) 80% marks in tutorial, terminal, home assignment and /or class examinations and (b) 20% marks for attendance in the class. The class teacher(s) of each course shall submit the average consolidated marks of class assessments and attendance in sealed envelope to the Chairman of the relevant examination committee within three weeks from the last class held.

Viva-voce examination includes the assessment of the students through oral examination of all the courses. No student shall be allowed to sit for the examination having less than 60% class attendance.

Course : Chem-531FOrganometallic Chemistry

Examination - 4 hoursFull Marks – 100(1 unit, 4 credit)

1. Application of different spectroscopic techniques to resolve structural problems of ligands and their complexes.

2. Organotransition-metal complexes of classic Lewis-base donors, phosphines and other group-VB donors and hydrides.

3. Unsaturated nitrogen ligands: macrocyclic imines, dinitrogen complexes, nitrous oxide, nitroso arenes, nitric oxide complexes, diazonium complexes, diazoalkane complexes, nitrite complexes, imines and nitrides.

4. Types of organometallic reactions:

a) Oxidative-additions: reaction with protons, reactions forming metal-carbon bonds, reaction with hydrogen.

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b) Reductive-eliminations: reaction forming carbon-carbon bonds, reactions forming carbon-hydrogen bonds.

c) Insertion reactions: migratory insertions, acyl formation, stereochemistry at the metal and alkyl carbon.

d) Intermolecular nucleophilic additions to unsaturated ligands: attack on coordinated CO, acyl, olefin, acytylene, arene, 3-allyl and 5-C5H5.

5. Chemistry of the iron group metallocenes: Ferrocene: preparation, electronic structure and bonding, physical properties, reactions, general aspects, comparative reactivities of ferrocene and bonzonoid aromatics, mechanism of electrophilic substitution, mechanism of the arylation reaction.

Recommended Books:1. Parcell and Kotz : Inorganic Chemistry 2. Cotton and Wilkinson : Advanced Inorganic Chemistry,

5th Edn. (1980)3. J.P. Collman and : Principles and Applications of

L.S. Hegedus Organo-transition Metal Chemistry4. J.E. Huheey : Inorganic Chemistry: Principles of

Structure and Reactivity5. J.D. Atwood : Inorganic and Organometallic

Reaction Mechanism. 6. W.U. Malik G.D. Tuli & : Selected Topics in Inorganic

R.D. Madan Chemistry7. S.Z. Haider : Selected Topics in Inorganic

Chemistry8. D.L. Pavia, G.M. Lavepman & : Introduction to Spectroscopy

G.S. Kriz (Saunders)

Course : Chem-532FBioinorganic ChemistryExamination - 4 hours

Full Marks - 100(1 unit, 4 credit)

1. General survey of the field. Trace element requirements, inorganic drugs (lithium and cis-platin etc.)

2. The biochemistry of iron :

(a) Iron storage and transport : Ferritin, transferrin, bacterial iron transport.

(b) Hemoglobin and myoglobin; nature of the heme- dioxygen binding, model system, cooperativity in hemoglobin.

(c) Cytochromes, cytochrome P450 enzymes.

(d) Iron-sulphur proteins, ferodoxins.

(e) Hemerythrins.

3. The biochemistry of other metals:

a) Zinc : carboxypeptidase (CPA and CPB) and carbonic anhydrase, (mechanism and model), metallothioneins.

b) Copper : Heme proteins and copper proteins in redox reactions, factors affecting redox potentials in metal complexes, catalase, peroxidase and superoxide dismutase, hemocyanins.

c) Cobalt : Vitamin B12 (structure and function) and coenzymes.

4. Metal and non-metals in biology and medicine : Metal pollution, cancer.

5. Nitrogen fixation.Recommended Books:1. Cotton and Wilkinson : Advanced Inorganic Chemistry,

5th Edn. (1980) 2. Counther L. Eichhorn : Inorganic Biochemistry, (edited) Vol. I & II3. J.E. Huheey : Inorganic Chemistry: Principles of

Structure and Reactivity.4. A.C. Deb : Fundamentals of Biochemistry5. K.F. Purcell & J.C. Kotz : Inorganic Chemistry 6. M.N. Hughes : The Inorganic Chemistry of

Biological Processes 7. R.J.P. Williams & De Silva : New Trends in Bioinorganic Chemistry8. E. Ochiai : Bioinorganic Chemistry:9. David R. Williams, (Edited) : An Introduction to Bioinorganic Chemistry10. R.W. Hay : Bioinorganic Chemistry11. D.M. Taylor, D:R. Williams : Trace Element, Medicine and

Chelation Therapy.

Course : Chem 533FInorganic Material Science

Examination - 4 hoursFull Marks – 100(1 unit, 4 credit)

1. Introduction to materials science and engineering: Materials and civilization, types of materials, materials and engineering, structure, properties, performance.

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2. Atomic bonding and coordination: Individual atoms and ions, molecules, macromolecules (polymers), three-dimensional bonding and interatomic distances.

3. Crystals (Atomic Order) : Crystalline phases, cubic structures, noncubic structures, polymorphism, unit-cell geometry, crystal directions, crystal planes and x-ray diffraction.

4. Disorder in solid phases: Imperfections in crystalline solids, noncrystalline materials, order and disorder in polymers, solid solutions, solid solutions in ceramic and metallic compounds and solid solutions in polymers (copolymers).

5. Polymers and composites: Deformation and flow of amorphous materials, processing of polymeric materials, polymeric composites, and properties of composites.

6. The physical properties of materials : Density, thermal properties, diffusion, electrical properties, magnetic properties, dielectric and optical properties.

7. Performance of materials in service: Service performance, corrosion reactions, corrosion control, delayed fracture, performance of metals at high temperatures, service performance of polymers, performance of ceramics at high temperatures.

Reference :1. Lawrence H. Van Vlack : Elements of Materials Science and

Engineering2. R.E. Smallman and R.J. Bishop : Metals and Materials3. O.P. Khanna : Material Science and Metallurgy

Course : Chem 534FAnalytical ChemistryExamination 4 hours

Full marks-100(1 unit, 4 credit)

1. Sampling : Water , air and soil, sample processing, trace analysis.

2. Atomic spectroscopy (10 Lectures): Absorption, emission and fluorescence methods: theory, measurement, interference and applications.

3. Electron spectroscopy: ESCA, AES (AUGER).

4. X-ray spectroscopy: Absorption, diffraction and fluorescence

5. Potentiometric methods (8 Lectures): Indicator electrodes, membrane indicator electrodes; glass electrode for pH measurements, liquid membrane electrodes, solid state and precipitate electrodes, pH meters, errors affecting pH measurements with glass electrodes, direct potentiometric measurements, calibration for direct potentiometry, standard addition method, potentiometric titrations, end point determination

6. Electrogravimetry and coulometry: Theory, instruments and applications.

7. Voltammetry and polarography (8 Lectures): Theory of hydrodynamic voltammetry and classical polarography; measurement and applications; anodic stripping voltammetry.

8. Thermal analysis: Differential thermal analysis and differential scanning calorimetry, thermogravimetry and thermometric titrations

9. Radiochemical methods: Radioactive isotopes, neutron activation analysis, isotopic dilution and radiometric methods.

Recommended Books:

1. D.A. Skoog : Principles of Instrumental Analysis (4th Ed.)

2. Willard, Merritt, Dean & Settle : Instrumental Methods of Analysis (6th Ed.)

3. Bassett, Danney, Jeffery & Mendhams : Vogel's Textbook of Quantitative Inorganic Analysis

4. Pavia, Lampman & Kriz : Introduction to Spectroscopy5. L.R. Faulkner & A.J. Bard : Electrochemical Methods

Course : Chem-535HHomogeneous and Heterogeneous Catalysis

Examination - 2 hoursFull Marks - 50

(0.5 unit, 2 credit)

1. Introduction: Definition and thermodynamics of catalysis, comparisons between homogeneous and heterogeneous catalysis, industrial application.

2. Inorganic reaction mechanism: i) Review of rate laws, activation parameters, substitution reaction on

sq. planar and octahedral complexes, electron transfer reactions.ii) Stereochemical non-rigidity. 3. Homogeneous catalysis:

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(i) Overview of mechanism, monohydride catalysts, dihydride catalysts.

(ii) General features of Wilkinson’s catalyst and mechanisms of hydrogenation by Rhodium (I) dihydride catalysts, asymmetric homogeneous hydrogenation, asymmetric catalysts of the type RhCIL3

and other asymmetric homogeneous catalysts.

4. Hydrogenation of olefin and acetylene: Hydrogenation of conjugated olefins and acetylene, hydrogenation of other functional groups, catalytic hydrogenation of arenes, a model for hydrogenase and free radical hydrogenation.

5. Synthesis characterization and Stoichiometric reactions of transition-metal hydrides.

6. Catalytic reaction involving carbon monoxide and hydrogen cyanide:

(i) Oxo reactions; cobalt catalysts, rhodium catalysts and other oxo catalysts

(ii) Fischer-Tropsch reaction; hydrogeneous Fischer-Tropsch catalysts, hydrogeneous model reactions and homogeneous CO hydrogenation.

Recommended Books:1. Parcell and Kotz : Inorganic Chemistry 2. Cotton and Wilkinson : Advanced Inorganic Chemistry,

5th Edn.(1980)3. J.P. Collman and : Principles and Applications of

L.S. Hegedus Organo-transition Metal Chemistry4. J.E. Huheey : Inorganic Chemistry: Principles of

Structure and Reactivity5. J.D. Atwood : Inorganic and Organometallic

Reaction Mechanism. 6. W.U. Malik G.D. Tuli & : Selected Topics in Inorganic Chemistry

R.D. Madan 7. S.Z. Haider : Selected Topics in Inorganic Chemistry

Course: Chem 536HEnvironmental Chemistry

Examination –2 Hours

Full marks-50

(40 lectures, 0.5 unit, 2 credit)

1. Introduction : Environmental science and environmental chemistry, definitions of some environmental terms, spheres of the environment, the natural cycles of environment.

2. Hydrosphere: Carbon dioxide in water, pH of natural water, behaviour of metal ions in water, complexing agents and humic substances in natural water, microbially mediated redox reactions.

3. Lithosphere : Composition of lithosphere, water and air in soil, inorganic and organic components in soil, acid-base and ion-exchange reactions in soil, micro- and macro-nutrients, wastes and pollutants in soil.

4. Trace Elements : Essential trace elements, pollution sources, Biochemical and toxicological effects of lead, mercury, cadmium and arsenic.

5. Noise Pollution: Classification, measurements of noise, noise pollution hazards and its controls.

Recommended Books:1. S.E. Manahar : Environmental Chemistry (6th Edn.)2. A.K. De : Environmental Chemistry (5th Edn.)3. S.S. Dara : A Text Book of Environmental Chemistry and

Pollution Control.4. Colin Baird : Environmental Chemistry.

Course : Chem-531L(Inorganic Chemistry Practical & Project)

Examination - 24 hoursFull Marks : 200 (2 unit, 8 credit)

Experiment & Project- 140Continuous Class Evaluation : 60

1. Preparation of 1-10 phenanthroline, ethylenediamine, orthophenyline diamine, picolinic acid, salicylic acid, oxalic acid, orthoamino benzoic acid

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complexes of Co(III), Cu(II), Ni(II), Cr(III), Fe(II), Fe(III); characterization by elemental, magnetic measurement & spectroscopic method.

2. Ion-exchange separation & estimation of some metal ions: Cu(II), Ni(II) Co(III) and some heavy metals.

3. Extraction & estimation of magnesium from green leaves

4. Estimation of arsenic in water.

5. Preparation of metal-acetylacetonate complexes and separation of metal complexes by chromatographic techniques.

6. Solvent extraction method: Separation & estimation of metal ions.

7. Preparation & characterization of thiocynate complexes of transition metals containing some monodentate & bidentate ligands.

8. Separation & estimation of metals from some inorganic drugs.

Recommended Books:1. J. Bassett & others : Vogel's Textbook of Quantitative

Inorganic Analysis2. Skoog & West : Fundamentals of Analytical Chemistry3. Schwarzenbach & Flaschka : Complexometric Titrations.