Chemistry (Minor) NEP Syllabus UG
Chemistry (Minor) NEP Syllabus UG
For the
Four Year Under Graduate Programme (FYUGP)
As per provisions of NEP-2020
Vinoba Bhave University Hazaribag
Subject: Chemistry
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Chemistry Minor
Chemistry may be opted as Minor-1 by the students having Major subject from
a) Natural & Physical Sciences (other than Chemistry) and
b) Mathematics, Statistics & Computer application streams.
It is intended to support the Major subject. There will be four papers of Chemistry minor of
4 credits each with following description:
i. Theory: 3 credits of 75 marks with pass marks 30.
ii. Practical: 1 credit of 25 marks with pass marks 10.
The chemistry Minor can be opted in odd semesters as follows:
Semester Minor paper No. of Credits
Theory Practical
I MN-1A (CHE) 3 Credits (75 Marks) 1 Credit (25 Credits)
(SIE=10+5, ESE =60) (SIE= 0, ESE =25)
III MN-1B (CHE) 3 Credits (75 Marks) 1 Credit (25 Credits)
(SIE=10+5, ESE =60) (SIE= 0, ESE =25)
V MN-1C (CHE) 3 Credits (75 Marks) 1 Credit (25 Credits)
(SIE=10+5, ESE =60) (SIE= 0, ESE =25)
VII MN-1D (CHE) 3 Credits (75 Marks) 1 Credit (25 Credits)
(SIE=10+5, ESE =60) (SIE= 0, ESE =25)
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Section A: Inorganic Chemistry-1
1. Atomic Structure: Review of Bohr’s theory and its limitations, dual behaviour of
matter and radiation, de-Broglie’s relation, Heisenberg Uncertainty principle,
Hydrogen atom structure, Need of a new approach to Atomic structure. Significance
of quantum numbers: Orbital angular momentum quantum numbers 𝑚𝑙 , Shapes of s,
p and d atomic orbitals, nodal planes. Discovery of spin, spin quantum number (s) and
magnetic spin quantum number (𝑚𝑠 ). Rules for filling electrons in various orbitals,
Electronic, configurations of the atoms, stability of half-filled and completely filled
orbitals, concept of exchange energy. Relative energies of atomic orbitals, Anomalous
electronic configurations.
(10 Lectures)
2. Chemical Bonding and Molecular Structure
Ionic Bounding: General characteristics of ionic bonding. Energy considerations in ionic
bonding, lattice energy and solvation energy and their importance in the context of
stability and solubility of ionic compounds. Statement of Born-Lande equation for
calculation of lattice energy, Born-Haber cycle and its applications, polarizing power
and polarizability, Fajan’s rules, ionic character in covalent compounds, bond
moment, dipole moment and percentage ionic-character.
Covalent bonding: VB Approach Shapes of some inorganic molecules and ions on the
basis of VSEPR and hybridization with suitable examples of linear, trigonal planar,
square planar, tetrahedral, trigonal bipyramidal and octahedral arrangements.
Concept of resonance and resonation structure in various inorganic and inorganic and
organic molecules/ions.
(10 Lectures)
2. Stereochemistry
Conformations with respect to ethane, butane and cyclohexane, Interconversion of
Wedge Formula, Newmann, Sawhorse and Fischer representation, Concept of chirality
(up to two carbon atoms). Configuration: Geometrical and Optical isomerism;
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Enantiomers, Diastereomers and Meso compounds. Threo- and erythro- D and L-cis–
trans nomenclature; CIP Rules; R/S (for up to 2 chiral carbon atoms) and E/Z
Nomenclature (for up to two C=C systems).
(7 Lectures)
3. Aliphatic hydrocarbons
Fundamental group approach for the following reactions (preparations & reactions)
to be studied in context to their structure.
a) Alkanes: (up to 5 Carbons). Preparation: Catalytic hydrogenation, Wurtz reaction,
Kolbe’s synthesis, from Grignard reagent. Reactions: Free radical Substitution:
halogenation.
b) Alkenes: (up to 5 Carbons) Preparation: Elimination reactions: Dehydration of
alkenes and dehydrohalogenation of alkyl halides (Saytzeff’s rule); cis alkenes
(Partial catalytic hydrogenation) and trans alkenes (Birch reduction). Reactions:
cis-addition (alk. KMnO4) and trans-addition (bromine), Addition of HX
(Markownikoff’s and anti-Markownikoff’s addition), hydration, Ozonolysis,
oxymercuration-demercuration, hydroboration-oxidation.
c) Alkynes: (up to 5 Carbons) Preparation: Acetylene from CaC2 and conversion into
higher alkynes; by dehalogenation of tetra halides and dehydrohalogenation of
vicinal-dihalides. Reactions: formation of metal acetylides, addition of bromine
and alkaline KMnO4. Ozonolysis and oxidation with hot alkaline KMnO4
(20 Lectures)
Reference Books:
1. J. D. Lee: A new Concise Inorganic chemistry, E. L. B. S.
2. F.A. Cotton & G. Wilknson: Basic Inorganic Chemistry, John Wiley.
3. Douglas, McDaniel and Alexader: Concepts and Models in Inorganic Chemistry, john
Wiely.
4. James E. Huheey, Ellen Keiter and Richard Keiter: Inorganic Chemistry: Principles of
Structure and Reactivity, Pearson Publication.
5. T.W. Graham Solomon: Organic Chemistry, John Wiely and Sons.
6. Peter Sykes: A Guide Book to Mechanism in Organic Chemistry, Orient Longman.
7. E.L.Eliel: Stereochemistry of Carbon Compounds, tata McGraw Hill.
8. I. L. Finar: Organic Chemistry (Vol. I & II), E. L. B. S.
9. R. T. Morrison & R. N. Boyd: Organic Chemistry. Prentice Hall.
10. Arun Bahl and B. S. Bahl: Advanced Organic Chemistry, S. Chand.
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MN-1A (Practical): Inorganic and Organic Chemistry
Reference Books:
1. Vogel’s Qualitative Inorganic Analysis, A. I. Vogel, Prentice Hall, 7th Edition.
2. Vogel’s Qualitative Chemical Analysis, A. I. Vogel, Prentice Hall, 6th edition.
3. Textbook of Practical Organic Chemistry, A. I. Vogel, Prentice Hall, 5th Edition.
4. Practical Organic Chemistry, F. G. Mann. & B. C. Saunders, Orient Longman, 1960.
Marks: 15 (5 Attd. + 10 SIE: 1Hr) + 60 (ESE: 3Hrs) = 75 Pass Marks: Th (SIE + ESE) = 30
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There will be two group of questions A and B. Group A is compulsory which will contain three
questions. Question No.1 will be very short answer type consisting of five questions of 1
mark each. Question No. 2 & 3 will be short answer type of 5 marks. Group B will contain
descriptive type five questions of fifteen marks each, out of which any three are to be
answered.
Note: There may be subdivisions in the questions of group B.
(8 Lectures)
2. Chemical Equilibrium:
Free energy change in a chemical reaction. Thermodynamic derivation of the law of chemical
equilibrium. Distinction between G and G0, Le Chatelier’s principle. Relationships between Kp,
KC and Kx for reactions involving ideal gases.
(5 Lectures)
3. Ionic Equilibria:
Strong, moderate and weak electrolytes, degree of ionization, factors affecting degree of
ionization, ionization constant ionic product to water, lionization of weak acids and bases, PH
for different types of salts solutions and buffer solutions. Solubility and solubility product of
sparingly soluble salts – applications of solubility product principle.
(7 Lectures)
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MN-1B (Practical): Physical and Organic Chemistry
Marks:0 (SIE) + 25 (ESE: 3Hrs) = 25 Pass Marks: = 10
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2. F. G. Mann& B. C. Saunders, Practical Organic Chemistry, Orient Longman (1960).
3. B. D. Khosla, Senior Practical Physical Chemistry, R. Chand & Co.
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Reversible and irreversible cells. Concept of EMF of a cell. Measurement of EMF of
a cell. Nernst equation and its importance. Types of electrodes. Standard electrode
potential. Electrochemical series. Thermodynamics of a reversible cell, calculation
of thermodynamics properties: G. H. and S from EMF data.
Section B: Organic Chemistry-3 ( 25 Lectures)
Functional group approach for the following reactions (preparations & reactions) to be
studied in context to their structure.
1. Carboxylic acids and their derivatives
Carboxylic acids (aliphatic and aromatic).
Preparation: Acidic and Alkaline hydrolysis esters.
Reactions: Hell-Vohlard- Zelinsky Reaction.
2. Carboxylic acid derivatives (aliphatic): (up to 5 carbons)
Preparation: Acid chlorides, Anhydrides, Esters and Amides from acids and their
interconversion.
Reactions: Comparative study of nucleophilicity of acyl derivatives. Reformatsky
Reaction, Perkin condensation.
3. Amines and Diazonium Salts
Amines (Aliphatic Aromatic): (up to 5 carbons)
Preparation: From alkyl halides, Gabriel’s Phthalimide synthesis, Hofmann
Bromamide reaction.
Reactions: Hofmann vs Saytzeff’s elimination, Carbylamine test, Hinsberg’s test,
with HNO2. Schotten – Baumann Reaction, Electrophilic substitution (case
aniline): nitration, bromination, sulphonation.
Diazonium salts: Preparation: from aromatic amines.
Reactions: Conversion to benzene, phenol, dyes.
4. Amino Acids, Peptides and Proteins:
Preparation of amino acids: Strecker synthesis using Gabriel’s Phthalimide
synthesis. Zwitterion, Isoelectric point and electrophoresis.
Reactions of amino Acids: ester of –COOH group, acetylation of –NH2 group,
complexation with Cu2+ ions, ninhydrin test.
Overview of Primary, Secondary, Tertiary and Quaternary structure of proteins.
5. Carbohydrates: Classification, General properties, Glucose and fructose (open
chain and cyclic structure), Determination of configuration of monosaccharides,
absolute configuration of Glucose and fructose, mutarotation, ascending and
descending in monosaccharides, Structure of disaccharides (sucrose, cellobiose,
maltose, lactose).
Reference Books:
1. G. W. Castellan: Physical Chemistry 4th Ed. Narosa (2004).
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2. J. C. Kotz, P. M. Treichel, J.R. Townsend, General Chemistry, Cengage Learning
India Pvt. Ltd. New Delhi (2009).
3. B. H. Mahan: University Chemistry, 3rd Ed. Narosa (1988).
4. R. H. Petrucci, General Chemistry, 5th Ed., Macmillan Publishing Co. New York
(1985).
5. Morrisin, R. T. & Boyd, R. N. Organic Chemistry, Dorling Kindersley (India) Pvt. Ltd.
(Pearson education).
6. Finar, I. L. Organic Chemistry (Volume 1), Dorling Kindersley (India) Pvt. Ltd.
(Pearson education).
7. Nelson, D. L. & Cox, M. M. Lehninger’s Principles of Biochemistry 7 th Ed., W. H.
Freeman.
8. Berg, J. M. Tymoczko, J. L. & Stryer, L. Biochemistry 7th Ed., W. H. Freeman.
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2. F. G. Mann& B.C. Saunders, Practical Organic Chemistry, Orient Longman (1960).
3. B. D. Khosla, Senior Practical Physical Chemistry, R. Chand & Co.
4. Ahluwalia, V. K. & Aggarwal, R. Comprehensive Practical Organic Chemistry,
Universities Press.
2. Solids:
Forms of solids, symmetry elements, unit cells, crystal systems, Bravais lattice types
and identification of lattice planes. Laws of Crystallography – Law of constancy of
interfacial angles, Law of rational indices. Miller indices. X-Ray diffraction by crystals,
Bragg’s law. Structures of NaCl, KCl and CsCl (qualitative treatment only).
Defects in crystals. Glasses and liquid crystals.
3. Chemical Kinetics
The concept of reaction rates. Effect of temperature, pressure, catalyst and other
factors on reaction rates. Order and molecularity of a reaction. Derivation of
integrated rate equations for zero, first and second order reactions (both for equal
and unequal concentrations of reactants). Half-life of a reaction. General methods for
determination of order of a reaction. Concepts of activation energy and its calculation
from Arrhenius equations.
Theories of Reactions Rates: Collision theory and activated complex theory of
bimolecular reactions. Comparison of the two theories (qualitative treatment only).
Reference Books:
1. G. W. Castellan: Physical Chemistry 4th Ed. Narosa (2004).
2. J. C. Kotz, P. M. Treichel, J.R. Townsend, General Chemistry, Cengage Learning India
Pvt. Ltd. New Delhi (2009).
3. B. H. Mahan: University Chemistry, 3rd Ed. Narosa (1988).
4. R. H. Petrucci, General Chemistry, 5th Ed., Macmillan Publishing Co. New York (1985).
5. J. D. Lee: A New Concise Inorganic Chemistry, E.L.B.S.
6. F. A. Cotton & G. Wilkinson: Basic Inorganic Chemistry, John Willey.
7. D. F. Shriver & P.W. Atkins: Inorganic Chemistry, Oxford University Press.
8. Gary Wulfsberg: inorganic Chemistry, Viva Books Pvt. Ltd.
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MN-1D (Practical): Inorganic and Physical Chemistry
Marks:0 (SIE) + 25 (ESE: 3Hrs) = 25 Pass Marks: = 10
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