BScSem3SyllabusAsPerNEP2020
BScSem3SyllabusAsPerNEP2020
BScSem3SyllabusAsPerNEP2020
Semester –III
Chemistry (Major-I) Organic Chemistry
BS23MJ3CH1
Learning Objectives: This core course aims to introduce the learner to the fascinating chemistry
of some biomolecules,i.e., carbohydrates, amino acids, peptides, proteins. It aims to build the
concept of amines, diazonium salts andheterocycles by the study of their physical properties,
synthesis routes and chemical reactions. The course will delve into various aspects of alkenes
and alkynes chemistry with specific emphasis on mechanistic studies.
Learning Outcomes: On completion of this course, the students will be able to: • demonstrate
understanding regarding classification, occurrence and synthesis of biomolecules such as
carbohydrates, proteins, peptides and amino acids. • Gain insight into chemistry of amines,
diazo compounds regarding their synthesis and physic-chemical properties. • Demonstrate
understanding of various aspects regarding chemical reactions such as mechanistic studies,
synthesis and reactivity of heterocyclic, alkenes and alkynes.
UNIT-1 [A] Carbohydrates
Carbohydrates Occurrence, classification and their biological importance. Monosaccharides:
Constitution and absolute configuration of glucose and fructose, epimers and anomers,
mutarotation, determination of ring size of glucose and fructose, Haworth projection and
conformational structures; Interconversion of aldoses and ketoses; Killiani-Fischer synthesis and
Ruff degradation.
[B]Amino acids, Peptides and their classification.
α-Amino Acids – Synthesis(Strecker’s and Gabriel’s Pthalimide), ionic properties and reactions.
Zwitterions, pKa values, isoelectric point and electrophoresis; Study of peptides: determination
of their primary structure-end group analysis. Synthesis of peptides using N-protecting, C-
protecting and C-activating groups, Solid-phase synthesis; primary, secondary and tertiary
structures of proteins, Denaturation of proteins.
UNIT 2[A] Amines
Introduction, classification, chirality in amines (pyramidal inversion), importance and general
methods of preparation. Properties: Physical properties, Basicity of amines: Effect of
substituents, solvent and steric effects. Distinction between Primary, secondary and tertiary
amines using Hinsberg’s method and nitrous acid. Discussion of the following reactions with
emphasis on the mechanistic pathway: Gabriel Phthalimide synthesis, Hoffmann- Bromamide
reaction, Carbylamine reaction, Mannich reaction, Hoffmann’s exhaustive methylation,
Hofmann-elimination reaction and Cope elimination.
[B] Diazonium Salts: Preparation and synthetic applications of diazonium salts including
preparation of arenes, haloarenes, phenols, cyano and nitro compounds. Coupling reactions of
diazonium salts (preparation of azo dyes)..
UNIT - 3 Heterocyclic Compounds
Introduction, importance, classification and nomenclature of heterocyclic compounds (containing
only one hetero atom). General discussion on the following aspects of heterocyclic compounds:
Structure, Aromaticity in 5-membered and 6-membered rings containing one heteroatom;
Basicity and relative reactivity towards electrophilic substitution reactions(amongst five
membered and six membered rings i.e. pyrrole, thiophene, furan, pyridine)
General methods of synthesis for: Furan, Pyrrole (Paal-Knorr synthesis, Knorr pyrrole synthesis,
Hantzsch synthesis), Thiophene, Pyridine (Hantzsch synthesis),Properties: Physical properties,
discussion on the following reaction (with mechanism) for Furan, Pyrrole, thiophene, Pyridine :
Electrophilic substitution- Nitration, sulphonation, halogenation, Formylation, acylation,
mercuration and carboxylation. Oxidation,Reduction, Addition, Reactions showing acidic /basic
character,Nucleophilic substitution reaction.
Unit 4[A] Alkenes
Addition to C=C: Mechanism, reactivity, regioselectivity (Markownikoffs and Anti-
Markownikoffs additions) and stereoselectivity. Reaction: Hydrogenations, Hydrohalogenation,
Hydration, Oxymercuration-demercuration, Hydroboration-Oxidation , ozonolysis, electrophilic
addition to diene (conjugated dienes and allene), reaction with NBS, Birch reduction of
Benzenoid aromatics, inter-conversion of E- and Z- alkenes.
[B] Alkynes
Addition to C≡C (in comparison to C=C): Mechanism, reactivity ,regioselectivity
(Markownikoffs and AntiMarkownikoffs additions) and stereo selectivity. Reaction:
Hydrogenations, Hydro halogenations, Hydration, Oxymercuration-demercuration,
Hydroboration-Oxidation, ozonolysis, Birch reduction of alkynes, reactions of terminal alkynes
by exploring its acidity.
REFERENCES
1. Berg, J.M.; Tymoczko, J.L.; Stryer, L. (2006),Biochemistry. W.H. Freeman and Co.
2. Nelson, D.L.; Cox, M.M.; Lehninger, A.L.(2009),Principles of Biochemistry. W.H. Freeman
and Co.
3. Murray, R.K., Granner, D.K., Mayes, P.A.; Rodwell, V.W.(2009),Harper’s Illustrated
Biochemistry.Lange Medical Books/McGraw-Hill. 4. Brown,T.A. (2018) Biochemistry, (First
Indian addition 2018) Viva Books.
4. Clayden, J., Greeves, N., Warren, S. Organic Chemistry, Second edition, Oxford University
Press 2012.
5. Sykes, P. A guidebook to Mechanism in Organic Chemistry, Pearson Education, 2003.
6. Smith, J. G. Organic Chemistry, Tata McGraw-Hill Publishing Company Limited.
7. Morrison, R. N. & Boyd, R. N. Organic Chemistry, Dorling Kindersley (India) Pvt. Ltd.
(Pearson Education).
8. Finar, I. L. Organic Chemistry (Volume 1), Pearson Education.
B. Sc. Semester –III
Chemistry (Major-II) Physical Chemistry
BS23MJ3CH1
Learning Objectives:The aim of this course is to make students understand third law of
thermodynamics and concept of absolute entropy, terms encountered in thermochemistry.
The students will be exposed to important concepts such as solutions, colligative properties,
adsorption and fundamentals of electrochemistry.
Learning Outcomes:By the end of the course, students will be able to Understand the third
law of thermodynamics and its applications. Derive various expressions of
thermochemistry.Explain the various conceptsregardingsolutions and colligative properties
and adsorption.Explain the basic terms of electrochemistry.
UNIT-3 Adsorption
Definition of terms, Types of adsorption, Applications of adsorption, Factors affecting
adsorption, Adsorption isobar and isostere, Desorption activation energy, Derivation of
Freundlich adsorption isotherm, Derivation of Langmuir adsorption isotherm, Types of
adsorption isotherms
UNIT– 4 Introduction of Electrochemistry
Electrodes, cell emf, emf and free energy, Standard electrode potentials, Nernst equation, emf
and activities, activity coefficients from emf’s, equilibrium constant from emf’s, electrode
concentration cells, electrolyte concentration cells, thermodynamic properties from cell
emf’s.
REFERENCES
1. Peter, A.; Paula, J. de. (2011), Physical Chemistry, 9th Edition, Oxford University Press.
2. Castellan, G. W. (2004),Physical Chemistry, 4th Edition, Narosa.
3. Kapoor, K.L.(2015),A Textbook of Physical Chemistry,Vol 2, 6th Edition, McGraw Hill
Education.
4. Kapoor, K.L.(2013),A Textbook of Physical Chemistry,Vol 3, 3rd Edition, McGraw Hill
Education.
5. McQuarrie, D. A.; Simon, J. D. (2004),Molecular Thermodynamics, Viva Books Pvt. Ltd.
BS23MJ3CH3
B. Sc. Semester –III
Chemistry (Major-III)
[Organic & Physical Practical]
Learning outcomes: After completion of course the students will be able to explain and perform
organic spotting and estimation. The students will be able to perform experiment regarding
measurements of temperature coefficient, strength of acids and conductometric titrations.
Estimations:(1)Glucose
(2) Ketone
(3) Phenol/Aniline
B. Physical Experiment
1. To determine the relative strength between HCl and H2SO4 by studying hydrolysis of
methyl acetate.
4. Conductometric titration.
(i) Strong acid vs Strong base (HCl vs NaOH)
(ii) Weak acid vs Strong base (CH3COOH vs NaOH)
(iii) Mixture of acids vs Strong base (HCl+CH3COOH vs NaOH)
5. To determine specific refraction and molar refraction of liquid A,B and their
mixture(OnlyDemo)
Learning Objectives: The objective of this course is to enhance the business and entrepreneurial
skills of undergraduate chemistry students and improve their employment prospects. The course
will orient the students to understand the Industry linkage with chemistry, challenges and
business opportunities. It will expose the students to the concepts of intellectual property rights,
patents and commercialisation of innovations.
Learning Outcomes: By the end of this course, students will be able to: Learn basics skills of
business and project management. Learn the process by which technical innovations are
conceived and converted into successful business ventures. Understand the intellectual property
rights and patents which drive business viability and commercialization of innovation. They will
effectively use the skills to contribute towards the well-being of the society and derive
commercial value.
Current challenges and opportunities for the chemistry based industries, Role of chemistry in
India and global economies,Supply chains of chemistry, important raw materials, Chemistry
based products in the market.
Business Basics
Key business concepts, Business plans, Market need, Project management, Routes to market,
Concept of entrepreneurship
Different stages of a project: Ideation, Bench work, Pilot trial, Production, Promotion/
Marketing, Intellectual Property Rights, Introduction to IPR & Patents, Agencies and regulators
for IPR in India, Funding agencies for startups.
REFERENCES
1. www.rsc.org
2. Nwaeke, L.I.(2002),Business Concepts and Perspectives, Springfield Publishers.
3. Silva, T. D. (2013),Essential Management Skills for Pharmacy and Business Managers, CRC
Press.
Shri Govind Guru University, Vinzol
B. Sc. Semester –III
BSC23VA301(IKS)
Learning objectives: To review & strengthen the ancient discovery and research in physics,
chemistry, maths, metallurgy, astronomy, architecture, textile, transport, agriculture and
Ayurveda etc. To help students to trace, identify and develop the ancient knowledge systems
to make meaningful contribution to development of science today.
Learning outcomes: After the completion of the course students will be able to trace
historical development of science and technology in Indian subcontinent. This course will
enhance students’ understanding regarding the research of ancient Indian scientists and will
help them to appreciate Indian culture of science and further build upon their research work.
REFERENCES
1. Stanley E. Manahan, 10th edition, Environmental chemistry, CRC Press, Taylor and
Francis Group, US, 2017
2. Baird, C. and Cann,M., Environmental Chemistry,(2012), Fifth Edition, W. H.
Freemann& Company, New York, US.
3. VanLoon, G.W. and Duffy, J.S.( 2018) Environmental Chemistry - A global
perspective, Fourth Edition, Oxford University Press
4. Brusseau, M.L.; Pepper,I.L. and Gerba, C., (2019) Environmental and Pollution
Science, Third Edition, Academic Press.
5. Masters, G.M., (1974) Introduction to Environmental Science and Technology, John
Wiley & Sons.
6. Masters, G.M., (2015) Introduction to Environmental Engineering and Science.
JPrentice Hall India Learning Private Limited.
7. De, A.K.(2012), Environmental Chemistry, New Age International Pvt., Ltd.
BS23MD3CH1
B. Sc. Semester –III ChemistryPractical (MDC)
[Organic Spotting]
REFERENCES
1. I Vogel, “Elementary Practical Organic Chemistry Part-II, Qualitative Organic
Analysis”, CBS Publishers & Distributers, New Delhi, SecondEdition,2004.
2. I Vogel,“Elementary Practical Organic Chemistry PartIII Quantitative
3. Organic Analysis”, CBS Publishers & Distributers, New Delhi,
SecondEdition,2004.
4. V.K. Ahluwalia, SunitaDhingra, “Comprehensive Practical Organic
Chemistry –Qualitative Analysis”, University Press (India) Private Limited,
Hyderabad, First Indian Edition,2010.