BSC Medical (General & Honours Scheme) - 21-5-19 For 2017 Batch

BSc Medical/Non-Medical/Chemistry Honours, BOS 21st May, 2019
Maharishi Markandeshwar(Deemed to be University)

Mullana-133207(Ambala), Haryana (India)
M. M. ENGINEERING COLLEGE, CHEMISTRY DEPARTMENT
(An ISO 9001-2002 Certified Institute)E-Mail: hod.chemistry@mmumullana.org, Tel. No.: 01731-304229
SCHEME FOR B.Sc. (Batch 2017-20 & 2018 onwards)

(Medical/Honors in Chemistry)
&
SYLLABUS FOR B.Sc. Medical/honours in Chemistry
[2017( 2nd & 3rd year) and 2018 onwards(1st to 6th Semester]
(12+3 SYSTEM OF EDUCATION)

Under
(Choice Based Credit System)
Chemistry Department
Maharishi Markandeshwar (Deemed to be University)
Mullana,Ambala,Haryana
INDIA-133207
SCHEME FOR B.Sc. (Medical)

Batch- 207-20 & 2018 onwards(CBCS)
SUMMARY
(SEMESTER SYSTEM)
B.Sc I, II & III (Medical)

1. Chemistry
2. Botany
3. Zoology
4. English (Ist Semester)
5. Environmental Science(IInd Semester)
6. Computer Applications(IIIrd Semester)
SUBJECT CODES
SUBJECT CODE USED
Chemistry BC
Botany BB
Zoology BZ
English BE
Environmental Science ES
IT Skills( Computer Applications) BIT
Name of the Discipline: B.Sc. (Medical)-General (CBCS)

(CHEMISTRY, BOTANY AND ZOOLOGY)-2017 onward
Sem. Core Course (Credit)(Hours) Ability Ability Elective Discipline Specific
Enhancement Enhancement (DSE)
Compulsory Course Elective Course (4)
(AECC) (2) (AEEC) (2)
(Skilled Based)
I Chemistry-I(4L+4P=8) (8hrs) (English)
Botany-I (4L+4P=8) (8hrs) Communication
Zoology-I(6+2=8)(8hrs) (2)(2 hrs)
General= Total Credit =20, Teaching hrs=26
II Chemistry-II (4L+4P=8) (8hrs) EVS(2)(2hrs)
Botany-II(4L+4P=8) (8hrs)
Zoology-II(6+2=8)(8hrs)
III Chemistry-III(4L+4P=8) (8hrs) SEC- I (2)(2
Botany-III(4L+4P=8) (8hrs) hrs) (IT Skills
Zoology-III(6+2=8)(8hrs) for Chemists)
IV Chemistry-IV(4L+4P=8) (8hrs) SEC-II(2)(2 hrs)
Botany-IV(4L+4P=8) (8hrs) (Chemistry)
Zoology-IV(6+2=8)(8hrs)
V SEC-III(2)(2 hrs) DSE-1(4L+4P=8)
(Botany) (8hrs)(Chemistry-V)
DSE-2(4L+4P=8) (8hrs)
(Botany-V)
DSE-3(4L+4P=8) (8hrs)
(Zoology-V)
VI SEC-IV(2)(2 hrs) DSE-4(4L+4P=8) (8hrs)
(Zoology) (Chemistry-VI)
DSE-5(4L+4P=8) (8hrs)
(Botany-VI)
DSE-6(4L+4P=8) (8hrs)
(Zoology-VI)
Total Credits= 120
SCHEME B.Sc. (Medical: July 2018 onwards)

CHOICE BASED CREDIT SYSTEM
FIRST SEMESTER
S.No. Cour Paper Paper Hrs/Week Cr. Marks

se Code Lecture Practical Tutorial T (Ex.+In.)
1 Core BC-111 Chemistry-I 4 - - 4 100(60+40)
2 Core BC-112 Chemistry Practical-I - 4 - 2 50(20+30)
3 Core BB-111 Botany-I 4 - - 4 100(60+40)
4 Core BB-112 Botany Practical-I - 4 - 2 50(20+30)
5 Core BZ-111 Zoology-I 4 - - 4 100(60+40)
6 Core BZ-112 Zoology Practical-I - 4 - 2 50(20+30)
7 AEC BE-111 English Communication 2 - - 2 50(30+20)
C
Total 14 12 - 20 500
THIRD SEMESTER (2017-20 & 2018 onwards)
S.No. Course Paper Paper Hrs/Week Cr. Marks

Code Lecture Practica Tutori T (Ex.+In.)
l al
1 Core BC-231 Chemistry-III 4 - - 4 100(60+40)
2 Core BC-232 Chemistry Practical-III - 4 - 2 50(20+30)
3 Core BB-231 Botany-III 4 - - 4 100(60+40)
4 Core BB-232 Botany Practical-III - 4 - 2 50(20+30)
5 Core BZ-231 Zoology-III 4 - - 4 100(60+40)
6 Core BZ-232 Zoology Practical-III - 4 - 2 50(20+30)
7 SEC BIT-231 IT Skills for chemists 2 - - 2 50(30+20)
Total 14 12 - 20 500
FIFTH SEMESTER(2017-20 & 2018 onwards)

Code Lecture Practical Tutorial T (Ex.+In.)
1 DSE BC-351 Chemistry-V 4 - - 4 100(60+40)
2 DSE BC-352 Chemistry Practical-V - 4 - 2 50(20+30)
3 DSE BB-351 Botany-V 4 - - 4 100(60+40)
4 DSE BB-352 Botany Practical-V - 4 - 2 50(20+30)
5 DSE BZ-351 Zoology-V 4 - - 4 100(60+40)
6 DSE BZ-352 Zoology Practical-V - 4 - 2 50(20+30)
7 SEC BC-353/ Analytical Clinical 2 - - 2 50(30+20)
Biochemistry
BB-353/
BZ-353
Total 14 12 - 20 500
SCHEME FOR -B. Sc. Medical with Honours in Chemistry-(2017-20 & 2018
onwards)
Sem. Core Course (Credit)(Hours) Ability Ability Elective Discipline

Enhancement Enhancement Specific (DSE)
Compulsory Course Elective Course (4)
(AECC) (2) (AEEC) (2)
(Skilled Based)
I Chemistry-I(4L+4P=8) (8hrs) (English) GE-1
Botany-I (4L+4P=8) (8hrs) Communication (Chemistry-I A)
Zoology-I(4L+4P=8)(8hrs) (2)(2 hrs) (4L+3P=7) (7hrs)
Total Credit =25.5 Teaching hrs=33
II Chemistry-II (4L+4P=8) (8hrs) EVS(2)(2hrs) GE-2
Botany-II(4L+4P=8) (8hrs) (Chemistry-II A)
Zoology-II(4L+4P=8)(8hrs) (4L+3P=7) (7hrs)
III Chemistry-III(4L+4P=8) (8hrs) IT Skills for GE-3
Botany-III(4L+4P=8) (8hrs) chemists- (Chemistry- III A)
Zoology-III(4L+4P=8)(8hrs) (SEC-I) (4L+3P=7) (7hrs)
Total Credit = 25.5 Teaching hrs=33
IV Chemistry-IV(4L+4P=8) (8hrs) SEC-II(2)(2 hrs) GE-4
Botany-IV(4L+4P=8) (8hrs) (Chemistry) (Chemistry- IV A)
Zoology-IV(4L+4P=8)(8hrs) (4L+3P=7) (7hrs)
V Chemistry-V(4L+4P=8) (8hrs) SEC-III(2)(2 hrs) GE-5
(Chemistry) (Chemistry- V)
Botany-V(4L+4P=8) (8hrs) (4L+3P=7) (7hrs)
Zoology-V(4L+4P=8)(8hrs)
VI Chemistry-VI(4L+4P=8) (8hrs) SEC-IV(2)(2 hrs) GE-6
(Chemistry) (Chemistry-VI A)
Botany-VI(4L+4P=8) (8hrs) (4L+3P=7) (7hrs)
Zoology-VI(4L+4P=8)(8hrs)
Total Credit = 153

SCHEME-B.Sc. (Medical with Honours in chemistry)

CHOICE BASED CREDIT SYSTEM-2018 onwards
THIRD SEMESTER

Code Lecture Practica Tutori T (Ex.+In.)
l al
3 Core BB-231 Botany-III 4 - - 4 100(60+40)
4 Core BB-232 Botany Practical-III - 4 - 2 50(20+30)
5 Core BZ-231 Zoology-III 4 - - 4 100(60+40)
6 Core BZ-232 Zoology Practical-III - 4 - 2 50(20+30)
8 GE BC-233 Chemistry-IIIA 4 - - 4 100(60+40)
9 GE BC-234 Chemistry Practical - - 3 - 1.5 50(20+30)
IIIA
Total 18 15 - 25.5 650
1 Core BC-351 Chemistry-V 4 - - 4 100(60+40)

2 Core BC-352 Chemistry Practical-V - 4 - 2 50(20+30)
3 Core BB-351 Botany-V 4 - - 4 100(60+40)
4 Core BB-352 Botany Practical-V - 4 - 2 50(20+30)
5 Core BZ-351 Zoology-V 4 - - 4 100(60+40)
6 Core BZ-352 Zoology Practical-V - 4 - 2 50(20+30)
7 SEC BC-353 Analytical Clinical Biochemistry 2 - - 2 50(30+20)
8 GE BC-354 Chemistry-VA 4 - - 4 100(60+40)
9 GE BC-355 Chemistry Practical -VA - 3 - 1.5 50(20+30)
Total 18 15 - 25.5 650
SCHEME FOR B.Sc. (Batch 2017-20 & 2018 onwards)

(Non-Medical/Honors in Chemistry)
&
SYLLABUS FOR B.Sc. Non-Medical/Honours in Chemistry
[2017(2nd & 3rd year) and 2018 onwards(1st to 6th Semester]
(12+3 SYSTEM OF EDUCATION)

Under
(Choice Based Credit System)
Chemistry Department
Maharishi Markandeshwar (Deemed to be University)
Mullana,Ambala,Haryana
INDIA-133207
SCHEME FOR B.Sc. (Non-Medical)

Batch- (2017-20 & 2018 onwards)(CBCS)
SUMMARY
(SEMESTER SYSTEM)
B.Sc I,II & III (Non-Medical)

2. Physics
3. Chemistry
4. Mathematics
5. English (Ist Semester)
7. Environmental Science(IInd Semester)
8. Computer Applications(IIIrd Semester)
SUBJECT CODES
SUBJECT CODE USED
Physics BP
Chemistry BC
Mathematics BM
English BE
Environmental Science ES
IT Skills( Computer Applications) BIT
B.Sc. Non-Medical (PHYSICS, CHEMISTRY,MATHEMATICS)

CHOICE BASED CREDIT SYSTEM (2017-onwards)
B. Sc. Non-medical
Sem. Core Course (Credit)(Hours) Ability Ability Elective Discipline Specific

Enhanceme Enhancement (DSE)
nt Elective Course (4)
Compulsory (AEEC) (2)
Course (Skilled Based)
(AECC) (2)
I Chemistry-I(4L+4P=8) (8hrs) (English)
Physics-I (4L+4P=8) (8hrs) Communicati
Maths-I(6+2=8)(8hrs) on
(2)(2 hrs)
II Chemistry-II (4L+4P=8) (8hrs) EVS(2)(2hrs)
Physics-II(4L+4P=8) (8hrs)
Maths-II(6+2=8)(8hrs)
III Chemistry-III(4L+4P=8) (8hrs) SEC- I (2)(2 hrs)
Physics-III(4L+4P=8) (8hrs) (IT Skills for
Maths-III(6+2=8)(8hrs) Chemists)
IV Chemistry-IV(4L+4P=8) (8hrs) SEC-II(2)(2 hrs)
Physics-IV(4L+4P=8) (8hrs) (Chemistry
Maths-IV(6+2=8)(8hrs)
V SEC-III(2)(2 hrs) DSE-1(4L+4P=8)
(Physics) (8hrs)(Chemistry-V)
DSE-2(4L+4P=8) (8hrs)
(Physics-V)
DSE-3(4L+4P=8) (8hrs)
(Maths-V)
VI SEC-IV(2)(2 hrs) DSE-4(4L+4P=8) (8hrs)
(Maths) (Chemistry-VI)
DSE-5(4L+4P=8) (8hrs)
(Physics-VI)
DSE-6(4L+4P=8) (8hrs)
(Maths-VI)
Total Credits = 126
Scheme for B.Sc. (Non-Medical: (2017-20 & 2018 onwards)

FIRST SEMESTER(2018 onwards)

Code Lecture Practic Tutoria T (Ex.+In.)
al l
1 Core BC-111 Chemistry-I 4 - - 4 100(60+40)
2 Core BC-112 Chemistry Practical-I - 4 - 2 50(20+30)
3 Core BP-111 Physics-I 4 - - 4 100(60+40)
4 Core BP-112 Physics Practical-I - 4 - 2 50(20+30)
5 Core BM-111 Mathematics-I 6 - 2 7 150(90+60)
6 AECC BE-111 English Communication 2 - - 2 50(30+20)
Total 16 08 2 21 500
THIRD SEMESTER (2017 onwards)

Code Lecture Practical Tutoria T (Ex.+In.)
l
3 Core BP-231 Physics-III 4 - - 4 100(60+40)
4 Core BP-232 Physics Practical-III - 4 - 2 50(20+30)
5 Core BM-231 Mathematics-III 6 - 2 7 150(90+60)
Total 16 08 2 21 500
FIFTH SEMESTER (2017 onwards)

al l
1 DSE BC-351 Chemistry-V 4 - - 4 100(60+40)
2 DSE BC-352 Chemistry Practical-V - 4 - 2 50(20+30)
3 DSE BP-351 Physics-V 4 - - 4 100(60+40)
4 DSE BP-352 Physics Practical-V - 4 - 2 50(20+30)
5 DSE BM-351 Mathematics-V 6 - 2 7 150(90+60)
6 SEC BC-353/ Analytical Clinical Biochemistry 2 - - 2 50(30+20)
BP-353/
BM-352
Total 16 08 2 21 500
B. SC. Non- Medical with Honours in Chemistry

SCHEME FOR CHOICE BASED CREDIT SYSTEM (2018 onwards)
Sem. Core Course (Credit)(Hours) Ability Ability Elective Discipline Elective Generic
Enhancement Enhancement Specific (DSE) (GE)(4)
Compulsory Elective (4)
Course (AECC) Course
(2) (AEEC) (2)
(Skilled
Based)
I Chemistry-I(4L+4P=8) (8hrs) (English) GE-1
Physics-I (4L+4P=8) (8hrs) Communication (Chemistry- I A)
Maths-I(6+2=8)(8hrs) (2)(2 hrs) (4L+3P=7) (7hrs)
Honours= Total Credits= 26.5 Teaching hours= 33
II Chemistry-II(4L+4P=8) (8hrs) EVS(2)(2hrs) GE-2
Physics-II (4L+4P=8) (8hrs) (Chemistry- II A)
Maths-II(6+2=8)(8hrs) (4L+3P=7) (7hrs)
III Chemistry-III(4L+4P=8) (8hrs) IT Skills for GE-3
Physics-III (4L+4P=8) (8hrs) (Chemistry- III A)
chemists-
Maths-III(6+2=8)(8hrs) (4L+3P=7) (7hrs)
(SEC-I)
IV Chemistry-IV(4L+4P=8) (8hrs) SEC-II(2)(2 GE-4 (Chemistry- IV
Physics-IV (4L+4P=8) (8hrs) hrs) A)
Maths-IV(6+2=8)(8hrs) (Chemistry) (4L+3P=7) (7hrs)
V Chemistry-V(4L+4P=8) (8hrs) SEC- III GE-5
(2)(2 hrs) (Chemistry- V A)
Physics-V (4L+4P=8) (8hrs) (4L+3P=7) (7hrs)
Maths-V(6+2=8)(8hrs) (Chemistry)

VI Chemistry-VI(4L+4P=8) (8hrs) SEC- IV GE-6
Physics-VI (4L+4P=8) (8hrs) (2)(2 hrs) (Chemistry- VI A)
Maths-VI(6+2=8)(8hrs) (Chemistry) (4L+3P=7) (7hrs)
Total Credit = 159
B.Sc. (Non-Medical with Honours in Chemistry)

CHOICE BASED CREDIT SYSTEM- (2017-20 & 2018 onwards)
THIRD SEMESTER (2017 onwards)

Code Lecture Practical Tutoria T (Ex.+In.)
l
1 Core BC-231 Chemistry –III 4 - - 4 100(60+40)
3 Core BP-231 Physics –III 4 - - 4 100(60+40)
4 Core BP-232 Physics Practical-III - 4 - 2 50(20+30)
5 Core BM-231 Mathematics-III 6 - 2 7 150(90+60)
7 GE BC-233 Chemistry-IIIA 4 - - 4 100(60+40)
8 GE BC-234 Chemistry Practical –IIIA - 3 - 1.5 50(20+30)
Total 20 11 2 26.5 650
FIFTH SEMESTER(2017 onwards)

al l
1 Core BC-351 Chemistry –V 4 - - 4 100(60+40)
2 Core BC-352 Chemistry Practical-V - 4 - 2 50(20+30)
3 Core BP-351 Physics –V 4 - - 4 100(60+40)
4 Core BP-352 Physics Practical-V - 4 - 2 50(20+30)
5 Core BM-351 Mathematics-V 6 - 2 7 150(90+60)
6 SEC BC-353 Analytical Clinical Biochemistry 2 - - 2 50(30+20)
7 GE BC-354 Chemistry-VA 4 - - 4 100(60+40)
8 GE BC-355 Chemistry Practical –VA - 3 - 1.5 50(30+20)
Total 20 11 2 26.5 650
SYLLABUS FOR
B.Sc. Medical/Non-medical/Honours
Courses in Chemistry
Batch 2017
(Only for 3rd year)
&
Batch 2018 onwards

(1st to 6th Semester)
----------------------------------------------------------------------------------------------------
Semester I
----------------------------------------------------------------------------------------------------
BSc Medical/Non-Medical (First Semester)
Chemistry-I
(2018 onwards)
Paper : Chemistry
Code : BC-111 Credits : 04
Total Marks: 100
Theory: 60
Sessional: 40
Time of Examination: 3 Hours
Learning Objectives: The course provides basic idea to the introductory topics of three major branches of
chemistry.
Learning Outcomes: After successful completion of the course, the students will have the knowledge of
structure of atom, types of bonding, basics of organic chemistry and the concepts of ionic equilibria.
NOTE: The Question paper is divided in to two sections A and B, both compulsory. Section A comprises
of 12 questions (3 from each unit) of one mark each. Section B comprises of 4 questions (1 from each unit
with two alternatives) of 12 marks each.
UNIT-I
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 spectra. Need of a new approach to Atomic structure.
Quantum mechanics, Time independent Schrodinger equation and meaning of various terms in it. Significance
of ψ and ψ2, Schrödinger equation for hydrogen atom. Radial and angular parts of the hydogenic wave functions
(atomic orbitals) and their variations for 1s, 2s, 2p, 3s, 3p and 3d orbitals (Only graphical representation).
Radial and angular nodes and their significance. Radial distribution functions and the concept of the most
probable distance with special reference to 1s and 2s atomic orbitals. Significance of quantum numbers, orbital
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.
UNIT-II
Chemical Bonding and Molecular Structure
Ionic Bonding: 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-
Landé 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.
(i) Covalent bond: Lewis structure, Valence Bond theory (Heitler-London approach). Energetics of
hybridization, equivalent and non-equivalent hybrid orbitals. Bent’s rule, Resonance and resonance energy,
Molecular orbital theory. Molecular orbital diagrams of diatomic and simple polyatomic molecules N2, O2, C2,
B2, F2, CO, NO, and their ions; HCl, BeF2, CO2, (idea of s-p mixing and orbital interaction to be given). Formal
charge, Valence shell electron pair repulsion theory (VSEPR), shapes of simple molecules and ions containing
lone pairs and bond pairs of electrons, multiple bonding (σ and π bond approach) and bond lengths. Covalent
character in ionic compounds, polarizing power and polarizability. Fajan’s rules and consequences of
polarization.Ionic character in covalent compounds: Bond moment and dipole moment. Percentage ionic
character from dipole moment and electronegativity difference.
UNIT-III
Basics of Organic Chemistry
Organic Compounds: Classification, and Nomenclature, Hybridization, Shapes of molecules, Influence of hybridization
on bond properties.
Electronic Displacements: Inductive, electromeric, resonance and mesomeric effects, hyperconjugation and their
applications; Dipole moment; Organic acids and bases; their relative strength. Homolytic and Heterolytic fission with
suitable examples. Curly arrow rules, formal charges; Electrophiles and Nucleophiles; Nucleophlicity and basicity; Types,
shape and their relative stability of Carbocations, Carbanions, Free radicals and Carbenes. Introduction to types of
organic reactions and their mechanism: Addition, Elimination and Substitution reactions.
Stereochemistry Conformations with respect to ethane, butane and cyclohexane. Interconversion of Wedge Formula,
Newmann, Sawhorse and Fischer representations. Concept of chirality (upto two carbon atoms). Configuration:
Geometrical and Optical isomerism; Enantiomerism, Diastereomerism and Meso compounds). Threo and erythro; D and
L; cis - trans nomenclature; CIP Rules: R/ S (for upto 2 chiral carbon atoms) and E / Z Nomenclature (for upto two C=C
systems).
UNIT_IV
Ionic Equilibria
Strong, moderate and weak electrolytes, degree of ionization, factors affecting degree of ionization, ionization constant
and ionic product of water. Ionization of weak acids and bases, pH scale, common ion effect; dissociation constants of
mono-, di- and triprotic acids (exact treatment). Salt hydrolysis-calculation of hydrolysis constant, degree of hydrolysis
and pH for different salts. Buffer solutions; derivation of Henderson
equation and its applications; buffer capacity, buffer range, buffer action and applications of buffers in analytical
chemistry and biochemical processes in the human body. Solubility and solubility product of sparingly soluble salts –
applications of solubility product principle. Qualitative treatment of acid – base titration curves (calculation of pH at
various stages). Theory of acid-base indicators; selection of indicators and their limitations.
Reference Books:
 Concept of resonance and resonating structures in various inorganic and organicLee, J.D. Concise Inorganic
Chemistry ELBS, 1991.
 Atkins, P.W. & Paula, J. Physical Chemistry, 10th Ed., Oxford University Press, 2014.
 Day, M.C. and Selbin, J. Theoretical Inorganic Chemistry, ACS Publications, 1962.
 Mortimer, R. G. Physical Chemistry 3rd Ed. Elsevier: NOIDA, UP (2009).
 Engel, T. & Reid, P. Physical Chemistry 3rd Ed. Pearson (2013).
 Morrison, R. N. & Boyd, R. N. Organic Chemistry, Dorling Kindersley (India) Pvt. Ltd. (Pearson Education).
 Finar, I. L. Organic Chemistry (Volume 1), Dorling Kindersley (India) Pvt. Ltd. (Pearson Education).
 Kalsi, P. S. Stereochemistry Conformation and Mechanism, New Age International, 2005.
BSc Medical/Non-Medical/Chemistry Honours (First Semester)

Chemistry Practical – I
(2018 onwards)
Paper : Chemistry Practical - I Credits : 02

Code : BC-112
Total Marks : 50
Practical/Viva voce : 20
Sessional : 30
Time of Examination : 4 Hours
Learning Objectives : To provide continued development of laboratory skills, interpretation of data and report
writing.
Learning Outcomes : On successful completion of the course students will be able to develop expertise
relevant to the professional practice of chemistry.
Introductory Labs
(i) Calibration and use of apparatus
(ii) Preparation of solutions of different Molarity/Normality of titrants
(iii) Checking the calibration of the thermometer
Section A
Inorganic Chemistry
Acid-Base Titrations
 Standardization of NaOH solution ( Standard solution of oxalic acid to be prepared)
 Estimation of carbonate and hydroxide present together in mixture.
 Estimation of carbonate and bicarbonate present together in a mixture.
 Estimation of free alkali present in different soaps/detergents/Shampoos
Section B
Organic Chemistry
 Purification of organic compounds by crystallization
using the following solvents:
Water
Alcohol
 Determination of the melting points of above compounds and unknown organic compounds.
 Effect of impurities on the melting point – mixed melting point of two unknown organic
compounds .
Section C
Physical Chemistry
pH metry
 Study the effect on pH of addition of HCl/NaOH to solutions of acetic acid, sodium acetate and their mixtures.
 Preparation of buffer solutions of different pH
o Sodium acetate-acetic acid
o Ammonium chloride-ammonium hydroxide

 pH metric titration of (i) strong acid vs. strong base, (ii) weak acid vs. strong base.
NOTE : 1. Any other experiment that can be conducted in the class.

2. Any value added experiment.
Reference Books :
 Mendham, J., A. I. Vogel’s Quantitative Chemical Analysis6th Ed., Pearson, 2009.

 Mann, F.G. & Saunders, B.C. Practical Organic Chemistry, Pearson Education (2009)
 Furniss, B.S.; Hannaford, A.J.; Smith, P.W.G.; Tatchell, A.R. Practical Organic Chemistry,5thEd., Pearson
(2012)
 Khosla, B. D.; Garg, V. C. & Gulati, A. Senior Practical Physical Chemistry, R. Chand & Co.: New Delhi
(2011).
 Garland, C. W.; Nibler, J. W. & Shoemaker, D. P. Experiments in Physical Chemistry8th Ed.; McGraw-Hill:
New York (2003).
B.Sc Medical/Non-Medical (First Semester)

COMMUNICATION SKILLS IN ENGLISH
(2018 onwards)
Paper: Communication skills in English Credits: 02
Code: BEN-111
Total Marks : 100
Theory : 60
Sessional : 40
Objective: The course aims to impart and nurture the skills of communication (grammar, vocabulary building, speaking,
reading and writing) required for the learners in their academic, social & professional pursuits. The course puts emphasis
on the practical usage of English.
Note: Eight questions will be set, two from each of the Sections I, II, III & IV. The Candidates are required to
attempt Five Questions in all, selecting at least one question from each Unit. All questions will carry equal marks.
UNIT-I
Essentials of Grammar
Parts of Speech
Common Errors
Voice--Active and Passive
UNIT-II
Vocabulary Building
Consulting Dictionary for Meaning, Usage and Pronunciation
One Word Substitution, Idioms
Synonyms and Antonyms
Homophones and Homonyms
UNIT-III
Writing Skills
Letter Writing (Official Letters)
Dialogue Writing
Objective Description
Developing Situations
Paragraph Writing
UNIT-IV
Speaking Skills
Presentation Skills
Introduction to Phonetics (IPA symbols)
Reading Skills
Comprehension
Precis Writing
BOOKS RECOMMENDED FOR STUDY
1) A Practical English Grammar by Thomson and Martinet

2) English Grammar and Composition by Rajendra Pal (Sultan Chand and Co. New Delhi)
3) High English Grammar and Composition by Wren and Martin (Sultan Chand and Co. New Delhi)
4) A Course in Phonetics and Spoken English J. D. Sethi and Dhamija ( Prentice Hall of India, New Delhi)
5) Business Correspondence and Report Writing by R.C.Sharma & Bishan Mohan ( Tata Mc. Graw Hill
Company, New Delhi)
6) The Functional Aspects of Communication Skills by P.Prasad and Rajendra K. Sharma (S.K.Kataria &
Sons, New Delhi)
7) Lesikar’s Basic Business Communication by Raymond Lesikar & Others(Mc. Graw –Hill Co. USA)
8) Oxford Advanced Learner Dictionary by A.S. Hornby (Oxford University Press)
9) English Pronouncing Dictionary by Daniel Jones (Cambridge University)
10) Improve Your Communication Skills, (Barker. A Kogan Page India Pvt Ltd, New Delhi)
11) The Oxford Guide to Writing and Speaking, (John Seely, Oxford University Press, New Delhi) (2004)
12) Effective Technical Communication, M. Ashraf Rizvi, (Tata Mc. Graw-Hill
Publishing Company Ltd.)
13) Communication Skills for Engineers and Scientists by Sangeeta Sharma & Binod Mishra,
(Pearson Education, New Delhi).
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Semester III
----------------------------------------------------------------------------------------------------
B.Sc. Medical / Non-Medical / Honours (Third Semester)
Chemistry – III
( 2017 onwards )
Paper : Chemistry-III Credits: 04

Code : BC-231
Total Marks : 100
Theory : 60
Sessional : 40
Learning Objectives : To impart advanced knowledge of representative elements of the periodic table,
some of the organic compounds and basics of thermodynamics
Learning Outcomes : The students will acquire knowledge of the essential elements required for all living
organisms, methods of preparation, properties and reactivity of alcohols, phenols, ethers, epoxides ans
sulphur containing compounds and various thermodynamic properties.
NOTE: The Question paper is divided in to two sections A and B, both compulsory. Section A
comprises of 12 questions (3 from each unit) of one mark each. Section B comprises of 4 questions (1
from each unit with two alternatives) of 12 marks each.
UNIT - I
Chemistry of s and p Block Elements-II

Study of the following compounds with emphasis on structure, bonding,
preparation, properties and uses:
Boric acid and borates, boron nitrides, borohydrides (diborane), carboranes and graphitic
compounds, silanes, Oxides and oxoacids of nitrogen, Phosphorus , sulphur and chlorine , interhalogen
compounds, polyhalide ions, pseudohalogens and basic properties of halogens. Noble Gases
General Physical properties, Low Chemical reactivity, Chemistry of Xenon , structure and bonding in
fluorides, oxides and oxyfluorides of Xenon
UNIT - II
Chemistry of Alcohols, Phenols, Ethers and Epoxides

Alcohols: preparation, properties and relative reactivity of 1°, 2°, 3°alcohols, Bouvaelt-Blanc Reduction;
Preparation and properties of glycols: Oxidation by periodic acid and lead tetraacetate, Pinacol-Pinacolone
rearrangement
Phenols: Preparation and properties; Acidity and factors effecting it, Ring substitution reactions,
Reimer–Tiemann and Kolbe’s–Schmidt Reactions, Fries and Claisen rearrangements with mechanism
Ethers and Epoxides: Preparation and reactions with acids. Reactions of epoxides with alcohols,
ammonia derivatives and LiAlH4
Sulphur containing compounds
Preparation and reactions of thiols, thioethers and sulphonic acids.
UNIT - III
Chemical Thermodynamics-I
Definition of thermodynamic terms: System, surroundings; types of systems; Intensive and extensive
variables; state and path functions; zeroth law of thermodynamics.
First law: Concept of heat, q, work, w, internal energy, U, and statement of first law; enthalpy, H, relation
between heat capacities, calculations of q, w, U and H for reversible, irreversible and free expansion of gases
(ideal and vander Waals) under isothermal and adiabatic conditions.
Thermochemistry: Heats of reactions: standard states; enthalpy of formation of molecules
and ions and enthalpy of combustion and its applications; calculation of bond energy, bond
dissociation energy and resonance energy from thermochemical data, effect of temperature (Kirchoff’s
equation) and pressure on enthalpy of reactions. Adiabatic flame temperature, explosion temperature.
UNIT - IV
Chemical Thermodynamics-II
Second Law: Concept of entropy; thermodynamic scale of temperature, statement of the second law of
thermodynamics; molecular and statistical interpretation of entropy.
Calculation of entropy change for reversible and irreversible processes.
Third Law: Statement of third law, concept of residual entropy, calculation of absolute entropy of molecules.
Free Energy Functions: Gibbs and Helmholtz energy; variation of S, G, A with T, V, P; Free energy
change and spontaneity. Relation between Joule-Thomson coefficient and other thermodynamic parameters;
inversion temperature; Gibbs-Helmholtz equation; Maxwell relations; thermodynamic equation of state.
Partial molar quantities, dependence of thermodynamic parameters on composition; Gibbs Duhem equation,
chemical potential of ideal mixtures, change in thermodynamic functions in mixing of ideal gases.
Reference Books:
• Lee, J.D. Concise Inorganic Chemistry , ELBS, 1991.
• Greenwood, N.N. & Earnshaw. Chemistry of the Elements, Butterworth Heinemann, 1997.
• Morrison, R. N. & Boyd, R. N. Organic Chemistry, Dorling Kindersley (India) Pvt. Ltd. (Pearson
Education).
• Finar, I. L. Organic Chemistry (Volume 1), Dorling Kindersley (India) Pvt. Ltd. (Pearson Education).
• Atkins, P. W. & Paula, J. de Atkin’s Physical Chemistry 10th Ed., Oxford University Press 2014.
• Assael, M.J.; Goodwin, A.R.H.; Stamatoudis, M.; Wakeham, W.A. & Will, S. Commonly Asked Questions
in Thermodynamics, CRC Press, NY, 2011.
BSc Medical/Non-Medical/Chemistry Honours (Third Semester )

Chemistry Practical – III
( 2017 onwards )
Paper : Chemistry Practical - III Credits: 02

Code : BC-232
Total Marks : 50
Practical/ Viva voce : 20
Sessional : 30
Learning Objectives : To develop the chemical synthetic and process technological skills
Learning Outcomes : At the end of course, the students will have an expertise in advanced titrimetric
methods of analysis, qualitative organic analysis, organic preparations and a silled hand in physical
instruments.
Section A : Inorganic Chemistry: Complexometric Titrations

 Principles of complexometric titrations
 Determination of concentration of Mg (II) & Zn (II) by titrimetric method using
EDTA.
 Determination of concentration of Ca/Mg in drugs or in food samples.
 Determination of concentration of total hardness of a given sample of water by
complexometric titration
Iodo / Iodimetric Titrations
 Estimation of Cu(II) and K2Cr2O7 using sodium thiosulphate solution (Iodimetrically).
 Estimation of (i) arsenite and (ii) antimony in tartar-emetic iodimetrically (iii)
Estimation of available chlorine in bleaching powder iodometrically.
Section B: Organic Chemistry: Organic preparations

To Carry out the following preparations using 0.5 - 1 g of starting compound. Recrystallize the product and
determine the melting point of the recrystallized sample.
1. To prepare acetanilide by the acetylation of aniline
2. To prepare p-bromoacetanilide.
3. Hydrolysis of benzamide or ethyl bezoate.
4. Nitration of nitrobenzene.
Section C : Physical Chemistry: Thermochemistry
 Determination of heat capacity of calorimeter for different volumes.

 Determination of enthalpy of neutralization of hydrochloric acid with sodium hydroxide.
 Determination of enthalpy of ionization of acetic acid.
 Determination of activation energy of dissolution of inorganic salts.
 Determination of integral enthalpy of solution of salts (KNO3, NH4Cl).
 Determination of enthalpy of hydration of copper sulphate.
 Study of the solubility of benzoic acid in water and determination of ΔH.
NOTE : 1. Any other related experiment that can be conducted in the lab.
Reference Books :
• Mann, F.G. & Saunders, B.C. Practical Organic Chemistry, Pearson Education (2009)
• Khosla, B. D.; Garg, V. C. & Gulati, A. Senior Practical Physical Chemistry, R. Chand & Co.: New Delhi
(2011).
• Garland, C. W.; Nibler, J. W. & Shoemaker, D. P. Experiments in Physical Chemistry8th Ed.; McGraw-Hill:
New York (2003).
• Ahluwalia, V.K. & Aggarwal, R. Comprehensive Practical Organic Chemistry: Preparation and
Quantitative Analysis, University Press (2000).
• Ahluwalia, V.K. & Dhingra, S. Comprehensive Practical Organic Chemistry: Qualitative Analysis,
University Press (2000).
• Mendham, J., A. I. Vogel’s Quantitative Chemical Analysis6th Ed., Pearson, 2009.
BSc Medical/Non-Medical/Chemistry Honours (Third Semester)

IT Skills for Chemists
(2017 onwards)
(SEC) Paper: IT Skills for Chemists
Credits: 02
Code: BIT-231
Total Marks : 50
Theory : 30
Sessional : 20
Learning Objectives: To develop practical hands in computers along with its theoretical knowledge.
Learning Outcomes : At the end of course, students will have enough knowledge to implement computers
in chemistry.
NOTE: The Question paper is divided in to two sections A and B, both compulsory.
Section A comprises of 6 questions (3 from each unit) of one mark each. Section B comprises of 2
questions (1 from each unit with two alternatives) of 12 marks each.
UNIT-I
Computer programming
Word Processing and Power Point

Introduction to word Processor and structure drawing (Chem Sketch) software. Word processing concepts, Use of
Templates, Working with word document: Edit ing text, Find and replace text, Formatting, spellcheck,
Autocorrect, Auto text; Bullets and numbering, Tabs, Paragraph Formatting, Indent, Page Formatting,
Header and footer, Tables: Inserting, filling and formatting a table; Inserting Pictures and Video;
Mail Merge: including linkingwith Database; Printing documents.
Creating Documents related to chemistry using the above facilities
Preparing Presentations
Basics of presentations: Slides, Fonts, D r a w i n g , Editing; I n s e r t i n g : Tables, Images, texts,
Symbols,Media;Design; Transition;Animation and Slideshow. Creating presentations using above facilities.
Spreadsheet software(EXCEL), Creating a spreadsheet, Managing worksheets; entering and formatting
information, basic functions and formulae and Printing a worksheet; Handling operators in formula,
Project involving multiple spreadsheets, Organizing Charts, t a b l e s and graphs. Incorporating tables and
graphs into a word processing document. Simple calculations, plotting graphs using spreadsheet (Planck’s
distribution Law, radial distribution curves for hydrogenic orbitals, gas kinetic theory) Generally used
S p r e a d s h e e t f u n c t i o n s :Mathematical, Statistical, Logical,Date and Time, Lookup and reference,
Database and Text functions.
UNIT-II
Mathematics
Fundamentals, mathematical functions, polynomial expressions, logarithms, the exponential function,
constants and variables, equation of a straight line, slope and intercept of the equation, slope and point
equation, two point equation, parallel lines, points of intersection, distance between two points, change of
origin. Examples from problems in chemistry, plotting graphs.
Logarithm Theory and application of logarithms for solving chemical problems.
Mean, Mode , Median, for grouped and ungrouped data. Variance and standard deviation
Numerical curve fitting: the method of least squares (regression).
Numerical methods of finding roots by bisection method, Regula Falsi and
Newton Raphson method.
Numerical differentiation by using Euler and R.K. Method.
Numerical integration by using Trapezoidal and Simpson’s rule.
Reference Books:
1. McQuarrie, D. A. Mathematics for Physical Chemistry University Science Books (2008). rd
2. Mortimer, R. Mathematics for Physical Chemistry. 3 Ed. Elsevier (2005). ]
3. Gupta. C.B. and Gupta.V. , An introduction to statistical methods,Vikas Publication(2005).
4. Steiner, E. The Chemical Maths Book Oxford University Press (1996).
5. Yates, P. Chemical calculations. 2 Ed. CRC Press (2007).
6. Harris, D. C. Quantitative Chemical Analysis. 6th Ed., Freeman (2007) Chapters 3-5.
7. Levie, R. de, How to use Excel in analytical chemistry and in general scientific data analysis,
Cambridge Univ. Press (2001) 487 pages.
8. Noggle, J. H. Physical chemistry on a Microcomputer. Little Brown & Co. (1985).
9. Venit, S.M. Programming in BASIC: Problem solving with structure and style. Jaico
Publishing House: Delhi (1996).
BSc Medical/Non-Medical/Chemistry Honours (Third Semester)

Chemistry – III A
( 2017 onwards)
Paper: Organometallic Chemistry Credits: 04

Code : BC-233
Total Marks : 100
Theory : 60
Sessional : 40
Learning Objectives: The course gives a thorough introduction to organometallic chemistry with a focus
on the transition metals. The course starts with fundamental molecular properties and gradually develops
this to practical applied catalysis. The application of organometallics in catalysis is highlighted with selected
important industrial processes.
Learning Outcomes: Completion of the course will provide students a good overview of the fundamental
principles of organotransition metal chemistry, knowledge about structure and bonding issues to understand
the stability and reactivity of simple organometallic complexes and important applications of organometallic
homogeneous catalysis in large and small scale production.
UNIT - I
Organometallic Compounds – I
Definition and classification of organometallic compounds on the basis of bond type. Concept of hapticity of
organic ligands.
Metal carbonyls: 18 electron rule, electron count of mononuclear, polynuclear and substituted metal
carbonyls of 3d series. General methods of preparation (direct combination, reductive carbonylation, thermal
and photochemical decomposition) of mono and binuclear carbonyls of 3d series. Structures of mononuclear
and binuclear carbonyls of Cr, Mn, Fe, Co and Ni using VBT. π-acceptor behaviour of CO (MO diagram of
CO to be discussed), synergic effect and use of IR data to explain extent of back bonding.
UNIT - II
Organometallic Compounds – II
Zeise’s salt: Preparation and structure, evidences of synergic effect and comparison of synergic effect with
that in carbonyls.
Metal Alkyls: Important structural features of methyl lithium (tetramer) and trialkyl aluminium (dimer),
concept of multicentre bonding in these compounds. Role of triethylaluminium in polymerisation of ethene
(Ziegler – Natta Catalyst). Species present in ether solution of Grignard reagent and their structures, Schlenk
equilibrium.
Ferrocene: Preparation and reactions (acetylation, alkylation, metallation, Mannich
Condensation). Structure and aromaticity. Comparison of aromaticity and reactivity with that of
benzene.
UNIT - III
Reaction Kinetics and Mechanism
Introduction to inorganic reaction mechanisms. Substitution reactions in
square planar complexes, Trans- effect, theories of trans effect, Mechanism of
nucleophilic substitution in square planar complexes, Thermodynamic and
Kinetic stability, Kinetics of octahedral substitution, Ligand field effects and reaction rates, Mechanism of
substitution in octahedral complexes.
UNIT - IV
Catalysis by Organometallic Compounds
Study of the following industrial processes and their mechanism:
1. Alkene hydrogenation (Wilkinson’s Catalyst)
2. Hydroformylation (Co and Rh salts)
3. Wacker Process
4. Monsanto acetic acid process
5. Water gas reactions
6. Synthetic gasoline (Fischer Tropsch reaction)
Reference Books:
• Cotton, F.A.; Wilkinson, G. & Gaus, P.L. Basic Inorganic Chemistry3rd Ed.; Wiley India,
• Huheey, J. E.; Keiter, E.A. & Keiter, R.L. Inorganic Chemistry, Principles of Structure and Reactivity 4th
Ed., Harper Collins 1993, Pearson,2006.
• Sharpe, A.G. Inorganic Chemistry, 4th Indian Reprint (Pearson Education) 2005
• Douglas, B. E.; McDaniel, D.H. & Alexander, J.J. Concepts and Models in Inorganic Chemistry3rd Ed.,
John Wiley and Sons, NY, 1994.
• Greenwood, N.N. & Earnshaw, A. Chemistry of the Elements, Elsevier 2nd Ed, 1997 (Ziegler Natta Catalyst
and Equilibria in Grignard Solution).
• Lee, J.D. Concise Inorganic Chemistry 5th Ed., John Wiley and sons 2008.
• Powell, P. Principles of Organometallic Chemistry, Chapman and Hall, 1988.
• Collman, J. P. et al.Principles and Applications of Organotransition Metal Chemistry. Mill Valley, CA:
University Science Books, 1987.
• Crabtree, R. H. The Organometallic Chemistry of the Transition Metals. j New York, NY: John Wiley, 2000.
• Spessard, G. O. & Miessler, G.L. Organometallic Chemistry. Upper Saddle River, NJ: Prentice-Hall, 1996.
BSc Medical/Non-Medical/Chemistry Honours (Third Semester )

Chemistry Practical – III A
( 2017 onwards)
Paper : Chemistry Practical -III A Credits: 1.5

Code : BC-234
Total Marks : 50
Sessional : 30
Learning Objectives : To provide scientific skills to the students in qualitative mixture analysis.
Learning Outcome : In this practical course, the students will acquire practical skills in inorganic
qualitative analysis.
Qualitative mixture analysis
Qualitative analysis of mixtures containing 3 anions and 3 cations. Emphasis should be given to the
understanding of chemistry of different reactions.
Radicals suggested:
CO3 , NO2 , S , SO3 , S2O3 , CH3COO , F- , Cl- , Br-, I- , NO3-, BO33-, C2O42- , PO43- , NH4+, K+,
2- - 2- 2- 2- -
Pb2+, Cu2+ , Cd2+, Bi3+ , Sn2+ , Sb3+ , Fe3+ , Al3+ , Cr3+, Zn2+ , Mn2+ , Co2+ , Ni2+ , Ba2 + , Sr2+, Ca2+, Mg2+
Mixtures should preferably contain one interfering anion, or insoluble component (BaSO4, SrSO4, PbSO4,
CaF2 or Al2O3) or combination of anions e.g. CO32- and SO32-, NO2- and NO3-, Cl- and Br-, Cl- and I-, Br- and
I-, NO3- and Br-, NO3- and I-.
Spot tests should be done whenever possible.
i. Measurement of 10 Dq by spectrophotometric method
ii. Verification of spectrochemical series.
iii. Controlled synthesis of two copper oxalate hydrate complexes: kinetic vs thermodynamic
factors.
iv. Preparation of acetylacetanato complexes of Mn2+/Cu2+ /Fe3+. Find the λmax of the complex.
v. Synthesis of ammine complexes of Ni(II) and its ligand exchange reactions (e.g. bidentate
ligands like acetylacetone, DMG, glycine) by substitution method.
Reference Books
• Vogel’s Qualitative Inorganic Analysis, Revised by G. Svehla. Pearson Education, 2002.
• Marr & Rockett Practical Inorganic Chemistry. John Wiley & Sons 1972.
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Semester V
----------------------------------------------------------------------------------------------------
BSc Medical/Non-Medical/Chemistry Honours (Fifth Semester)
Chemistry-V
(2017 onwards)
Paper : Chemistry-V Credits : 04

Code : BC-351
Total Marks : 100
Theory: 60
Sessional: 40
Learning Objectives : The course intends to enlighten the students on the chemistry of acids and
bases, nitrogen containing organic compounds, polynuclear hydrocarbons and electrochemistry.
Learning Outcomes : The students will acquire a knowledge about the general inorganic chemistry,
a few organic compounds and electrochemistry
UNIT – I
Acids and Bases
Brönsted-Lowry concept of acid-base reactions, solvated proton, relative strength of acids, types of acid-base reactions,
levelling solvents, Lewis acid-base concept, Classification of Lewis acids, Hard and Soft Acids and Bases (HSAB)
Application of HSAB principle.
General Principles of Metallurgy

Chief modes of occurrence of metals based on standard electrode potentials. Ellingham diagrams for reduction of
metal oxides using carbon and carbon monoxide as reducing agent. Electrolytic Reduction, Hydrometallurgy. Methods
of purification of metals: Electrolytic Kroll process, Parting process, van Arkel-de Boer process and Mond’s process,
Zone refining.
UNIT – II
Nitrogen Containing Functional Groups
Preparation and important reactions of nitro and compounds, nitriles and isonitriles ; Amines:
Effect of substituent and solvent on basicity; Preparation and properties: Gabriel phthalimide
synthesis, Carbylamine reaction, Mannich reaction, Hoffmann’s exhaustive methylation,
Hofmann-elimination reaction; Distinction between 1°, 2° and 3° amines with Hinsberg

reagent and nitrous acid. Diazonium Salts: Preparation and their synthetic applications.
UNIT – III
Polynuclear Hydrocarbons
Reactions of naphthalene phenanthrene and anthracene Structure, Preparation and
structure elucidation and important derivatives of naphthalene and anthracene;
Polynuclear hydrocarbons.
UNIT – IV
Electrochemistry
Quantitative aspects of Faraday’s laws of electrolysis, rules of oxidation/reduction of ions based on half-cell potentials,
applications of electrolysis in metallurgy and industry. Chemical cells, reversible and irreversible cells with examples.
Electromotive force of a cell and its measurement, Nernst equation; Standard electrode (reduction) potential and its
application to different kinds of half-cells. Application of EMF measurements in determining (i) free energy, enthalpy
and entropy of a cell reaction, (ii) equilibrium constants, and (iii) pH values, using hydrogen, quinone-hydroquinone,
glass and SbO/Sb2O3 electrodes. Concentration cells with and without transference, liquid junction potential;
determination of activity coefficients and transference numbers.
Reference Books:
• Glasstone, S., An Introduction to Electrochemistry, East West press pvt. Ltd.
• Brette, C.M..A. & Brette, A. O., Electrochemistry- Principles, methods and applications, Oxford University Press ,
Inc., Newyork, Ist Edn.(1993)
• Bard, A.J. & Faulkner L.R.,Electrochemical methods – Fundamental and applications, 2nd Ed., John Wiley & Sons,
Inc. ,Newyork
• Morrison, R. T. & Boyd, R. N. Organic Chemistry, Dorling Kindersley (India) Pvt. Ltd. (Pearson Education).
• Finar, I. L. Organic Chemistry (Volume 1), Dorling Kindersley (India) Pvt. Ltd. (Pearson Education).
• Finar, I. L. Organic Chemistry (Volume 2: Stereochemistry and the Chemistry of Natural Products), Dorling
Kindersley (India) Pvt. Ltd. (Pearson Education).
• Lee, J.D., Concise Inorganic Chemistry, ELBS, 1991.
• Miessler, G. L. & Donald, A. Tarr. Inorganic Chemistry 4th Ed.,Pearson, 2010.
• Atkin, P. Shriver & Atkins’ Inorganic Chemistry 5th Ed. Oxford University Press (2010).

Chemistry Practical – V
( 2017 onwards)
Paper: Chemistry Practical - V Credits: 02

Code: BC-352
Total Marks: 50
Practical/ Viva voce: 20
Sessional : 30
Learning Objectives: To provide a skilled practical hand in quantitative analysis, qualitative organic
analysis and experimental skills in potentiometric titrations.
Learning Outcomes: The students will acquire practical skills in quantitative and qualitative analysis and
titrations.
Section A : Inorganic Chemistry: Gravimetric Analysis:

 Estimation of nickel (II) using Dimethylglyoxime (DMG).
 Estimation of copper as CuSCN
 Estimation of iron as Fe2O3 by precipitating iron as Fe(OH)3.
 Estimation of Al (III) by precipitating with oxine and weighing as Al(oxine)3 (aluminium oxinate).
Section B: Organic Chemistry: Qualitative Analysis

 Detection of extra elements.
 Qualitative analysis of unknown organic compounds containing simple
functional groups (alcohols, carboxylic acids, phenols and carbonyl
compounds) and preparation of respective derivatives.
 Functional group test for nitro, amine and amide groups with their
respective derivative preparation.
Section C: Physical Chemistry: Potentiometry

Perform the following potentiometric titrations:
 Strong acid vs. strong base
 Weak acid vs. strong base
 Dibasic acid vs. strong base
 Potassium dichromate vs. Mohr's salt
Adsorption
 Verify the Freundlich and Langmuir isotherms for adsorption of acetic acid on activated charcoal.
Reference Books:
 Mendham, J., A. I. Vogel’s Quantitative Chemical Analysis,6th Ed., Pearson, 2009.

 Ahluwalia, V.K. & Aggarwal, R. Comprehensive Practical Organic Chemistry: Preparation and
Quantitative Analysis, University Press (2000).
 Ahluwalia, V.K. & Dhingra, S. Comprehensive Practical Organic Chemistry: Qualitative Analysis,
University Press (2000).
 Khosla, B. D.; Garg, V. C. & Gulati, A. Senior Practical Physical Chemistry, R. Chand & Co.: New Delhi
(2011).
 Garland, C. W.; Nibler, J. W. & Shoemaker, D. P. Experiments in Physical Chemistry8th Ed.; McGraw-Hill:
New York (2003).

Analytical Clinical Biochemistry
( 2017 onwards)
(SEC) Paper : Analytical Clinical Biochemistry Credits: 02

Code: BC-353
Total Marks : 50
Theory: 30
Sessional : 20
Learning Objectives: This course on analytical clinical biochemistry intends to enlighten the students
on the knowledge of various biomolecules supporting life processes and their laboratory testing.
Learning Outcomes: Completion of the course will provide students enough information and
testing modes of the carbohydrates, proteins, lipids, enzymes, DNA and RNA.
NOTE: The Question paper is divided in to two sections A and B, both compulsory.
Section A comprises of 6 questions (3 from each unit) of one mark each. Section B
comprises of 2 questions (1 from each unit with two alternatives) of 12 marks each.
UNIT – I
Basic understanding of the structures, properties and functions of carbohydrates, lipids and proteins
Carbohydrates: Biological importance of carbohydrates, Metabolism, Cellular currency of energy (ATP), Glycolysis,
Alcoholic and Lactic acid fermentations, Krebs cycle. Isolation and characterization of polysachharides.
Identification and estimation of the following:

1. Carbohydrates – qualitative and quantitative.
2. Lipids – qualitative
Proteins: Classification, biological importance; Primary and secondary and tertiary structures of proteins: α-helix and
β- pleated sheets, Isolation, characterization, denaturation of proteins.
1. Qualitative identification of Proteins

2. Isolation of protein.
3. Determination of protein by the Biuret reaction.
Enzymes: Nomenclature, Characteristics (mention of Ribozymes), Classification; Active site, Mechanism of enzyme
action, Stereospecificity of enzymes, Coenzymes and cofactors, Enzyme inhibitors, Introduction to Biocatalysis:
Importance in “Green Chemistry” and Chemical Industry.
UNIT – II
Lipids: Classification. Biological importance of triglycerides and phosphoglycerides and cholesterol; Lipid membrane,
Liposomes and their biological functions and underlying applications.
1. Determination of the iodine number of oil.

2. Determination of the saponification number of oil.
Structure of DNA (Watson-Crick model) and RNA, Genetic Code, Biological roles of DNA and RNA: Replication,
Transcription and Translation, Introduction to Gene therapy. .
1. Determination of nucleic acids
Biochemistry of disease: A diagnostic approach by blood/ urine analysis.
Blood: Composition and functions of blood, blood coagulation. Blood collection and preservation of samples.
Anaemia, Regulation, estimation and interpretation of data for blood sugar, urea, creatinine, cholesterol and bilirubin.
1. Determination of cholesterol using Liebermann- Burchard reaction
Urine: Collection and preservation of samples, Formation of urine. Composition and estimation of constituents of
normal and pathological urine.
Reference Books:
• Cooper, T.G. Tool of Biochemistry. Wiley-Blackwell (1977).
• Wilson, K. & Walker, J. Practical Biochemistry. Cambridge University Press (2009).
• Varley, H., Gowenlock, A.H & Bell, M.: Practical Clinical Biochemistry, Heinemann, London (1980).
• Devlin, T.M., Textbook of Biochemistry with Clinical Correlations, John Wiley & Sons, 2010.
• Berg, J.M., Tymoczko, J.L. & Stryer, L. Biochemistry, W.H. Freeman, 2002.
• Talwar, G.P. & Srivastava, M. Textbook of Biochemistry and Human Biology, 3rd Ed. PHI Learning.
• Nelson, D.L. & Cox, M.M. Lehninger Principles of Biochemistry, W.H. Freeman, 2013.

Chemistry – V A
( 2017 onwards)
Paper : Applied Organic Chemistry Credits: 04

Code : BC-354
Total Marks : 100
Theory : 60
Sessional : 40
Learning Objectives : This course on organic chemistry intends to make students get an idea about
various natural products like alkaloids, terpenes alongwith dyes, polymers and different synthetic drugs and
pharmaceuticals.
Learning Objectives: In this course, the students will acquire knowledge about the chemistry of natural
products, dyes, polymers and medicinal organic chemistry.
UNIT – I
Drugs & Pharmaceuticals
Drug discovery, design and development; Basic Retrosynthetic approach. Synthesis of the representative
drugs of the following classes: analgesics agents, antipyretic agents, antiinflammatory agents (Aspirin,
paracetamol, lbuprofen); antibiotics (Chloramphenicol); antibacterial and antifungal agents (Sulphonamides;
Sulphanethoxazol, Sulphacetamide, Trimethoprim); antiviral agents (Acyclovir), Central Nervous System
agents (Phenobarbital, Diazepam),Cardiovascular (Glyceryl trinitrate), antilaprosy (Dapsone), HIV-AIDS
related drugs (AZT- Zidovudine).
UNIT – II
Dyes
Classification, Colour and constitution; Mordant and Vat Dyes; Chemistry of dyeing; Synthesis and
applications of: Azo dyes – Methyl Orange and Congo Red (mechanism of Diazo Coupling); Triphenyl
Methane Dyes -Malachite Green, Rosaniline and Crystal Violet; Phthalein Dyes – Phenolphthalein and
Fluorescein; Natural dyes –structure elucidation and synthesis of Alizarin and Indigotin; Edible Dyes with
examples.
UNIT – III
Polymers
Introduction and classification including di-block, tri-block and amphiphilic polymers; Number
average molecular weight, Weight average molecular weight, Degree of polymerization, Polydispersity
Index. Polymerisation reactions -Addition and condensation -Mechanism of cationic, anionic and free
radical addition polymerization; Metallocene-based Ziegler-Natta polymerisation of alkenes;
Preparation and applications of plastics – thermosetting (phenol-formaldehyde, Polyurethanes) and
thermosoftening (PVC, polythene); Fabrics – natural and synthetic (acrylic, polyamido, polyester);
Rubbers–natural and synthetic: Buna-S, Chloroprene and Neoprene; Vulcanization; Polymer additives;
Introduction to liquid crystal polymers; Biodegradable and conducting polymers with examples
UNIT – IV
Alkaloids
Natural occurrence, General structural features, Isolation and their physiological action . Hoffmann’s exhaustive
methylation, Emde’s modification, Structure elucidation and synthesis of Hygrine and Nicotine. Medicinal
importance of Nicotine, Hygrine, Quinine, Morphine, Cocaine, and Reserpine.
Terpenes
Occurrence, classification, isoprene rule; Elucidation of stucture and synthesis of Citral, Neral and α-
terpinol.
Reference Books:
 Morrison, R. T. & Boyd, R. N. Organic Chemistry, Dorling Kindersley (India) Pvt. Ltd. (Pearson
Education).
 Patrick, G. L. Introduction to Medicinal Chemistry, Oxford University Press, UK, 2013.
 Singh, H. & Kapoor, V.K. Medicinal and Pharmaceutical Chemistry, Vallabh Prakashan,
Pitampura, New Delhi, 2012.
 Foye, W.O., Lemke, T.L. & William, D.A.: Principles of Medicinal Chemistry, 4th Ed., B.I.
Waverly Pvt. Ltd. New Delhi.
 Finar, I. L. Organic Chemistry (Volume 1& 2), Dorling Kindersley (India) Pvt. Ltd. (Pearson Education).
 Singh, J.; Ali, S.M. & Singh, J. Natural Product Chemistry, Prajati Parakashan (2010).
 Berg, J.M., Tymoczko, J.L. & Stryer, L. (2006) Biochemistry. 6th Ed. W.H. Freeman and Co.

Chemistry Practical – V A
( 2017 onwards)
Paper : Chemistry Practical -V A Credits: 01.5

Code : BC-355
Total Marks : 50
Sessional : 30
Learning Objectives: To provide hands on extraction and isolation of plant pigments and food other
products and preparation of polymers, dyes and pharmaceuticals.
Learning Outcomes: On successful completion of this practical course, the students will be able to perform
synthetic, extractive and qualitative operations.
Practicals
1. Extraction of caffeine from tea leaves.
2. Extraction of β-carotene from carrot/ seasonal vagetables.
3. Isolation of casein from milk.
4. Isolation of lactose from milk.
5. Preparation of sodium polyacrylate.
6. Preparation of urea formaldehyde.
7. Analysis of Carbohydrate: aldoses and ketoses, reducing and non-reducing sugars.
8. Qualitative analysis of unknown organic compounds containing monofunctional groups (carbohydrates, aryl halides,
aromatic hydrocarbons) and simple bifunctional groups, for e.g. salicylic acid, cinnamic acid, nitrophenols, etc.
9. Preparation of Aspirin.
10. Preparation of paracetamol
11. Preparation of methyl orange.
Reference Books:
• Vogel, A.I. Quantitative Organic Analysis, Part 3, Pearson (2012).
• Singh J., Advanced Practical Chemistry, Pragati Prakashan(2012).
• Ed.; W.H. Freeman & Co.: New York (2003).

BSC Medical (General & Honours Scheme) - 21-5-19 For 2017 Batch

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BSc Medical/Non-Medical/Chemistry Honours, BOS 21st May, 2019

Maharishi Markandeshwar(Deemed to be University)

SCHEME FOR B.Sc. (Batch 2017-20 & 2018 onwards)

(12+3 SYSTEM OF EDUCATION)

SCHEME FOR B.Sc. (Medical)

B.Sc I, II & III (Medical)

Name of the Discipline: B.Sc. (Medical)-General (CBCS)

SCHEME B.Sc. (Medical: July 2018 onwards)

S.No. Cour Paper Paper Hrs/Week Cr. Marks

THIRD SEMESTER (2017-20 & 2018 onwards)

S.No. Course Paper Paper Hrs/Week Cr. Marks

FIFTH SEMESTER(2017-20 & 2018 onwards)

S.No. Course Paper Paper Hrs/Week Cr. Marks

Sem. Core Course (Credit)(Hours) Ability Ability Elective Discipline

Total Credit = 153

SCHEME-B.Sc. (Medical with Honours in chemistry)

S.No. Course Paper Paper Hrs/Week Cr. Marks

1 Core BC-351 Chemistry-V 4 - - 4 100(60+40)

SCHEME FOR B.Sc. (Batch 2017-20 & 2018 onwards)

(12+3 SYSTEM OF EDUCATION)

SCHEME FOR B.Sc. (Non-Medical)

B.Sc I,II & III (Non-Medical)

B.Sc. Non-Medical (PHYSICS, CHEMISTRY,MATHEMATICS)

Sem. Core Course (Credit)(Hours) Ability Ability Elective Discipline Specific

Scheme for B.Sc. (Non-Medical: (2017-20 & 2018 onwards)

FIRST SEMESTER(2018 onwards)

THIRD SEMESTER (2017 onwards)

FIFTH SEMESTER (2017 onwards)

B. SC. Non- Medical with Honours in Chemistry

Honours= Total Credits= 26.5 Teaching hours= 33

B.Sc. (Non-Medical with Honours in Chemistry)

THIRD SEMESTER (2017 onwards)

S.No. Course Paper Paper Hrs/Week Cr. Marks

FIFTH SEMESTER(2017 onwards)

S.No. Course Paper Paper Hrs/Week Cr. Marks

Batch 2018 onwards

Chemical Bonding and Molecular Structure

Basics of Organic Chemistry

BSc Medical/Non-Medical/Chemistry Honours (First Semester)

Paper : Chemistry Practical - I Credits : 02

o Ammonium chloride-ammonium hydroxide

NOTE : 1. Any other experiment that can be conducted in the class.

 Mendham, J., A. I. Vogel’s Quantitative Chemical Analysis6th Ed., Pearson, 2009.

B.Sc Medical/Non-Medical (First Semester)

BOOKS RECOMMENDED FOR STUDY

1) A Practical English Grammar by Thomson and Martinet

Paper : Chemistry-III Credits: 04

Chemistry of s and p Block Elements-II

Chemistry of Alcohols, Phenols, Ethers and Epoxides

BSc Medical/Non-Medical/Chemistry Honours (Third Semester )

Paper : Chemistry Practical - III Credits: 02

Section A : Inorganic Chemistry: Complexometric Titrations

Section B: Organic Chemistry: Organic preparations

 Determination of heat capacity of calorimeter for different volumes.

 Study of the solubility of benzoic acid in water and determination of ΔH.

BSc Medical/Non-Medical/Chemistry Honours (Third Semester)

Word Processing and Power Point

BSc Medical/Non-Medical/Chemistry Honours (Third Semester)

Paper: Organometallic Chemistry Credits: 04

BSc Medical/Non-Medical/Chemistry Honours (Third Semester )

Paper : Chemistry Practical -III A Credits: 1.5

Paper : Chemistry-V Credits : 04

General Principles of Metallurgy