Syllabus
M.Sc. Final Chemistry
M.Sc. (2nd) Theory
Specialization
(Organic Chemistry)
CHE-551
Paper I: Reaction Mechanisms, Pericyclic MM:60
Reaction, Photochemistry and
Stereochemistry
Block I : ORGANIC REACTION
MECHANISMS – II
Unit
– 1 : Reaction intermediates – I
Unit
– 2 : Reaction intermediates – II
Unit
– 3 : Molecular rearrangements – I
Unit
– 4 : Molecular rearrangements – II
Unit
– 5 : Elimination reactions
Block II : PERICYCLIC REACTIONS
Unit
– 6 : Classification and stereochemistry of pericyclic reactions
Unit
– 7 : Molecular orbitals and their symmetry properties
Unit
– 8 : Analysis of electrocyclic reactions
Unit
– 9 : Analysis of cycloaddition reactions
Unit
– 10 : Analysis of sigmatropic reactions
BLOCK III : ORGANIC PHOTOCHEMISTRY
Unit
– 11 : Electronic transistions
Unit
– 12 : Photochemistry of carbonyl compounds
Unit
– 13 : Photochemistry of alkenes and dienes
Unit
– 14 : Photochemistry of benzene derivatives
Unit
– 15 : Photochemistry of peroxides, nitrites, hypohalites, azo compounds and
Diazo compounds
BLOCK IV : STEREOCHEMISTRY – II
Unit
– 16 : Conformations of some acyclic molecules
Unit
– 17 : Conformations of disubstituted cyclohexanes, cyclohexenes and
Monosubstituted cyclohexanes
Unit
– 18 : Conformation of disubstituted cyclohexanes, cyclohexanes and
Cyclohexanones
Unit
– 19 : Conformations of a few other monocyclic and bicyclic systems
Unit
– 20 : Conformation and reactivity
CHE-
552 Papers II: Synthetic Organic Chemistry
MM: 60
BLOCK I: ORGANIC SYNTHESIS-I
Unit
–1: A brief review of
functionalisation and functional group transformation reactions
And oxidation of alkanes and
alkenes
Unit
– 2: Oxidation of alcohols
Unit
– 3: Reduction by catalytic
hydrogenations
Unit
– 4: Reduction by hydride transfer
agents
Unit
– 5 : Reductions by dissolving metals.
BLOCK II :ORGANIC SYNTHESIS – II
Unit
– 6: Formation of carbon-carbon single
bond
Unit
– 7: Formation of carbon-carbon double
bond
Unit
– 8: Synthetic applications of
organoboranes
Unit
– 9: Synthetic applications of
organosilanes
Unit
– 10: Protecting groups in organic synthesis
BLOCK III : SYNTHETIC STRATEGIES
Unit
– 11 : Introduction, target selection
and terminology
Unit
– 12 : Disconnection approach with
examples
Unit
– 13 : Strategic bond in carbocyclic
and heterocyclicsystems
Unit
– 14 : Applications of some important
strategies in organic synthesis
Unit
– 15 : Some selected synthesis
BLOCK IV : ASYMETRIC SYNTHESIS
Unit
– 16 : Topicity, configurational
descritors and stereoselectivity
Unit
– 17 : Principles of asymmetric
synthesis and analysis of stereoisomer mixtures
Unit
– 18 : Substrate controlled methods
Unit
– 19 : Auxilliary controlled methods
Unit
– 20 : Reagent controlled and catalyst
controlled synthesis
CHE-553 Paper III:
Natural Products, Heterocycles and Spectroscopy MM: 60
BLOCK I : NATURAL PRODUCTS – II
Unit
– 1: Alkaloids
Unit
– 3: Prostaglandins
Unit
– 4: Vitamins
Unit
– 5: Rotenoids and porphyrins
BLOCK II : ENZYMES AND BIOGENISIS
Unit
– 6: Enzymes and their reactivity
Unit
– 7: Biochemical path ways – I
Unit
– 8: Metabolism of fatty acids and proteins
Unit
– 9: Biosynthetic methods, general methods and feeding experiments
Unit –10: Biosynthesis
aromatic hydro carbons by acetate/malonate and
Shikimic acid pathway
BLOCK III : HETEREOCYCLIC COMPOUNDS
Unit
– 11 : Membered hetereocycles containing two hetero atoms
Unit
– 12 : Membered heterocycles containing more than two hetero atoms
Unit
– 13 : Membered heterocycles containing two hetero atoms
Unit
– 14 : Synthesis of pyrimidine, purine and xanthine bases
Unit
– 15 : And 4-membered heterocyclic compounds
BLOCK IV : SPECTROSCOPY – III
Unit – 16 : 13C NMR spectroscopy – I
Unit
– 17 : 13C NMR spectroscopy – ii
Unit
– 18 : 19F, 31P NMR spectroscopy
Unit
– 19 : Multipulse sequences in NMR spectroscopy
Unit
– 20 : Optical rotatory dispersion studies (ORD)
CHE-554 Paper IV: Drugs
and PharmaceuticaMM60
BLOCK 1 : DRUG DISCOVERY, DESIGN
AND DEVELOPMENT
Unit
– 1 : Drug discovery, design and development
Unit
– 2 : Concepts of receptors, agonists and antagonists
Unit
– 3 : Drug development of Salbutamol, cimetidine and captopril
Unit
– 4 : Structure activity relationship studies – I
Unit
– 5 : SAR studies – II Development of oxaminiquine & SAR studies of
Sulphonamides and benzepines
BLOCK 2 : DRUGS ACTING ON DIFFERENT
TARGETS – I
Unit
– 6 : Combinatorial synthesis
Unit
– 7 : Quantitative structure activity relationships – (QSAR)
Unit
– 8 : Pharmacokinetics, prodrugs and clinical trials
Unit
– 9 : Drugs acting on metabolic process
Unit
– 10 : Drugs acting on cell walls and cell membranes
BLOCK 3 : DRUGS ACTING ON DIFFERENT
TARGETS – II
Unit
– 11 : Drugs acting on the nervous system
Unit
– 12 : enzyme inhibitors
Unit
– 13 : Drugs effecting cholinergic nervous system
Unit
– 14 : Drugs acting on histamine receptors and ion channels
Unit
– 15 : Drugs acting on genetic material
BLOCK 4 : MANUFACTURE AND ANALYSIS
OF DRUGS
Unit
– 16 : Introduction to chiral drugs
Unit
– 17 : Synthesis of chiral drugs
Unit
– 18 : Drugs and drug intermediate from fermentation
Unit
– 19 : Drug analysis
Unit
– 20 : Quality control methods in drug manufacturing and formulations
BLOCK 1 : DRUG DISCOVERY, DESIGN
AND DEVELOPMENT
This
block deals with drug discovery, design and development; it is divided into five
units:
Unit
– 1 : Drug discovery, design and development
Unit
– 2 : Concepts of receptors, agonists and antagonists
Unit
– 3 : Drug development of Salbutamol, cimetidine and captopril
Unit
– 4 : Structure activity relationship studies – I
Unit
– 5 : SAR studies – II Development of oxainiquine & SAR studies of
sulphonamides
benzodiazepines
Paper
V: Practical MM:200
|
Syllabus M.Sc. Previous Chemistry
session 2013-2014 M.Sc.
|
|
CHE501
|
INORGANIC CHEMISTRY
|
|
UNIT SCHEDULE
|
BLOCK 1
|
SYMMETRY OF MOLECULES
|
|
Unit 1
|
Symmetry Operations and Symmetry Elements
|
|
Unit 2
|
Mathematical Rules of Groups – Abelian and
Non-Abelian
|
|
Unit 3
|
Molecular Point Groups
|
|
Unit 4
|
Group Multiplication Tables
|
|
Unit 5
|
Symmetry and Properties of Molecules –
Molecular Polarity, Chirality and Optical Activity
|
|
BLOCK 2
|
THEORIES OF BONDING AND ELECTRONIC SPECTRA
OF METAL COMPLEXES
|
|
Unit 6
|
Crystal Field Theory – Splitting of Metal
d-Orbitals in Different Geometries
|
|
Unit 7
|
Ligand Field Parameters
|
|
Unit 8
|
Molecular Orbital Theory
|
|
Unit 9
|
Free Ion Terms and Energy Levels
|
|
Unit 10
|
Orgel Diagrams
|
|
BLOCK 3
|
REACTION MECHANISMS OF TRANSITION METAL
COMPLEXES
|
|
Unit 11
|
Labile and Inert Complexes
|
|
Unit 12
|
Substitution Reaction Mechanisms of
Octahedral complexes
|
|
Unit 13
|
Substitution Reaction Mechanisms of Square
Planar complexes
|
|
Unit 14
|
Electron Transfer Reaction Mechanisms
|
|
Unit 15
|
Reaction Mechanisms of Organometallic
Compounds
|
|
BLOCK 4
|
|
|
Unit 16
|
Stability constants of Metal Complexes and
Factors Influencing Stability
|
|
Unit 17
|
Methods of Determination of Stability
Constants
|
|
Unit 18
|
Ligational aspects of Diatomic Molecules
|
|
Unit 19
|
Metal Clusters
|
|
Unit 20
|
Coordination Chemistry of Metal Ions in
Biomolecules
|
|
CHE502
|
ORGANIC CHEMISTRY
|
|
UNIT SCHEDULE
|
BLOCK 1
|
STEREOCHEMISTRY OF ORGANIC COMPOUNDS
|
|
Unit 1
|
Molecular representation and classification
of stereoisomers
|
|
Unit 2
|
Molecular symmetry and chirality
enantiomers and disastereoisomers
|
|
Unit 3
|
Molecules with one and more than one chiral
centers
|
|
Unit 4
|
Absolute configurational nomenclature
determination of configuration and resolution of racemates
|
|
Unit 5
|
Axial,
planar and helical chirality and ii- or e, z- diastereoisomerism
|
|
BLOCK 2
|
ORGANIC REACTION MECHANISM
|
|
Unit 6
|
Basic concepts, electronic effects,
electro-negativity resonance, acid and basic character of organic
|
|
Unit 7
|
Reaction pathways
|
|
Unit 8
|
Electrophilic addition to carbon-carbon
double bonds
|
|
Unit 9
|
Aliphatic nucleophilic substitution
|
|
Unit 10
|
Neighbouring group participation, ambident
nucleophiiles, aromatic nucleophilic substitution and aliphatic electrophilic
substitution
|
|
BLOCK
|
3 AROMATICITY, BENZENOID NON-BENZENOID
AROMATIC COMPOUNDS AND HETEROCYCLIC COMPOUNDS
|
|
Unit 11
|
Concept of aromaticity
|
|
Unit 12
|
Nonbenzenoid aromatic compounds synthesis
and reactions of 3,5,7- mebered carobcyclic systems
|
|
Unit 13
|
Azulenes and polycyclic aromatic compounds
|
|
Unit 14
|
Heterocyclic compounds
|
|
Unit 15
|
Fused hetero bicyclic and tricyclic
systems: carbazole, quinoline isoquinoline and acridine
|
|
BLOCK
|
4 NATURAL PRODUCTS
|
|
Unit 16
|
Natural products terpenes and terpenoids
|
|
Unit 17
|
Alkaloids
|
|
Unit 18
|
Carbohydrates monosaccharides
|
|
Unit 19
|
Carbohydrates disaccharides
|
|
Unit 20
|
Carbohydrates polysaccharides
|
|
CHE503
|
PHYSICAL CHEMISTRY
|
|
UNIT SCHEDULE
|
BLOCK 1
|
QUANTUM CHEMISTRY
|
|
Unit 1
|
Basic quantum chemistry
|
|
Unit 2
|
Wave Mechanics of some simple systems with
Constant potential energy
|
|
Unit 3
|
Hydrogen – like atoms
|
|
Unit 4
|
Approximation Methods and Interaction of
Radiation and Matter
|
|
Unit 5
|
Theories of Chemical Bonding – Diatomic
Molecules
|
|
BLOCK 2
|
THERMODYNAMICS
|
|
Unit 6
|
Concept of Thermodynamic Law – First law of
Thermodynamics
|
|
Unit 7
|
The Second law of thermodynamics
|
|
Unit 8
|
Spontaneity and Equilibrium
|
|
Unit 9
|
Ideal and Non-ideal solutions and activity
coefficients
|
|
Unit 10
|
Nernst Heat Theorem and Thirst law of
Thermodynamics
|
|
BLOCK 3
|
ELECTRO CHEMISTRY
|
|
Unit 11
|
Electrochemical Cells First law of
thermodynamics
|
|
Unit 12
|
Polarization
|
|
Unit 13
|
Electro Analytical Techniques
|
|
Unit 14
|
Activity
|
|
Unit 15
|
Corrosion
|
|
BLOCK 4
|
CHEMICAL KINETICS AND PHOTO CHEMISTRY
|
|
Unit 16
|
Theories of Reaction rates
|
|
Unit 17
|
Kinetics of Complex Reactions
|
|
Unit 18
|
Reactions in Solutions
|
|
Unit 19
|
Photochemistry
|
|
Unit 20
|
Photochemical Reaction Mechanisms
|
|
CHE504
|
SPECTROSCOPY, COMPUTERS AND MATHEMATICS/
BIOLOGY
|
|
UNIT SCHEDULE
|
BLOCK 1
|
MATHEMATICS FOR BIOLOGY STUDENTS
|
|
Unit 1
|
Co-ordinate System
|
|
Unit 2
|
Differential Calculus
|
|
Unit 3
|
Matrics
|
|
Unit 4
|
Integral Calculus
|
|
Unit 5
|
Differential Equations
|
|
BLOCK 2
|
BIOLOGY
|
|
Unit 6
|
Cell Structure and Functions
|
|
Unit 7
|
Carbohydrates
|
|
Unit 8
|
Fatty Acids
|
|
Unit 9
|
Amino Acids, Peptides and Proteins
|
|
Unit 10
|
Nucleic Acids
|
|
BLOCK 3
|
SPECTROSCOPY – I
|
|
Unit 11
|
Rotational Spectra
|
|
Unit 12
|
Vibrational Spectroscopy – 1
|
|
Unit 13
|
Vibrational Spectroscopy – 2
|
|
Unit 14
|
Vibrational Spectroscopy – 3
|
|
Unit 15
|
Roman Spectroscopy
|
|
Unit 16
|
Electron Spectroscopy
|
|
BLOCK 4
|
SPECTROSCOPY – II
|
|
Unit 17
|
H NMR Spectroscopy – 1
|
|
Unit 18
|
H NMR Spectroscopy – 2
|
|
Unit 19
|
NMR of Paramagnetic Compounds
|
|
Unit 20
|
Mass Spectrometry – 1
|
|
Unit 21
|
Mass Spectrometry – 2
|
|
BLOCK 5
|
COMPUTERS
|
|
Unit 22
|
Introduction to Compounds
|
|
Unit 23
|
Basic Language
|
|
Unit 24
|
C Language
|
|
Unit 25
|
Chemistry Applications using Basic
Programme
|
|
Unit 26
|
Chemistry Application using C Language
|
|
PRACTICAL
COURSE
|
|
||
|
CHE505
|
INORGANIC
CHEMISTRY
|
|
|
UNIT SCHEDULE
|
BLOCK
1
|
INORGANIC
SALT MIXTURE SEMI-MICRO QUALITATIVE ANALYSIS
|
|
Unit
1
|
Introduction
to Semi Micro Analysis
|
|
Unit
2
|
Classification
of Cations Into Groups for Qualitative Analysis
|
|
Unit
3
|
Reactions
of Cations
|
|
Unit
4
|
General
Group Seperation and Analysis of Individual Groups
|
|
Unit
5
|
Model
Semi – Micro Analysis of Cations (A Known Salt Mixture-I)
|
|
Unit
6
|
Model
Semi – Micro Analysis of Cations (A Known Salt Mixture-II) Record analysis of unknown Salt Mixture
|
|
BLOCK
2
|
PREPARATION,
CALIBRATION AND VOLUMETRIC ESTIMATIONS
|
|
Unit
7
|
1.
Preparation of Complexes Tetrammine Copper (II)
Sulphate. Hydrate
2.
Preparation of hexamine nickel (II) chloride [Ni
(NH3)6] Cl2
3.
Preparation of Chloropentammine Cobalt (III)
chloride
4.
Preparation of (Tris) Diaminoethane Nickel (II)
Sulphate [Ni (en)3] SO4
5.
Preparation of Sodium (tris) Oxalatoferrate (III)
Na3 [Fe (C2O4)3]
|
|
Unit
8
|
Calibration
of Analytical Apparatus
|
|
Unit
9
|
1.
Estimation of Ca2+ by Substitution
Titration Using EDTA
2.
Estimation of Ni2+ by back Titration
Using EDTA
3.
Estimation of Mn2+ and Mg2+
by back Titration Using EDTA
|
|
Unit
10
|
1. Estimation of
Cu in [Fe(c2o4)3]
2. Estimation of
Fe in Na3 [Fe (C2o4)3]
3. Determination
of ion exchange Capacity of a Resin.
|
|
BLOCK
3
|
ESTIMATION
INVOLVING VOLUMETRY AND GRAVIMETRY
|
|
Unit
11
|
Estimation
of Cu2+ and Ni2+ Present in a sample Solution
|
|
Unit
12
|
Estimation
of Ag+ and Ca2+ in a Sample Solution
|
|
CHE506
|
ORGANIC
CHEMISTRY
|
|
UNIT SCHEDULE
|
BLOCK
1
|
ACCIDENTS
IN LABORATORY – FIRST AID
|
|
Unit
1
|
Safety
in Chemical Laboratory
|
|
BLOCK
2
|
METHODS
AND MANIPULATION
|
|
Unit
2
|
Laboratory
Equipment & Technique
|
|
BLOCK
3
|
SYSTEMATIC
QUALITATIVE ANALYSIS OF CARBON COMPOUNDS
|
|
Unit
3
|
Systematic
Qualitative analysis of a model organic compounds
|
|
Unit
4
|
Systematic
Qualitative analysis of a model organic compounds
|
|
Unit
5
|
Identification
of organic compounds by systematic qualitative analysis
|
|
BLOCK
4
|
PREPARATION
OF ORGANIC COMPOUNDS
|
|
Unit
6
|
1. Preparation of
1,2,3,4,6- Penta-O-acetyl – β-D glucopyranose
2. Preparation of
2,4,6 – Tribromo Aniline
3. Preparation of
1,3,5 – Tribromo Benzene
4. Preparation of
1,3 – Dinitro Benzene
|
|
Unit
7
|
1. Preparation of
m-Nitro Aniline
2. Preparation of
2,4-Dihydroxy Acetophenone
3. Preparation of
4-Methyl – 7 – hydroxyl coumarin
|
|
Unit
8
|
1. Preparation of
Benzoly glycine
2. Preparation of
1,2,3,4 – Tetrahydro carbazole
3. Preparation of
9,10 – Dihydro anthracene -9, 10- α,β – Succinic anhydride
|
|
BLOCK
5
|
QUANTITATIVE
ORGANIC ANALYSIS
|
|
Unit
9
|
Estimation
of Phenol
|
|
Unit
10
|
Estimation
of Primary Aromatic Amine
|
|
Unit
11
|
Estimation
of Methyl Ketone
|
|
Unit
12
|
Estimation
of reducing sugars
|
|
BLOCK
6
|
CHROMATORAPHY
– SEPARATION TECHNIQUE
|
|
Unit
13
|
1. Chromatography
2. Paper
Chromatography
3. Gas-Liquid
Chromatography
|
|
Unit
14
|
Seperation
of a solid mixture by column chromatography
|
|
CHE507
|
PHYSICAL CHEMISTRY
|
|
UNIT SCHEDULE
|
BLOCK 1
|
PHYSICAL PROPERTIES & DISTRIBUTION
STUDY
|
|
Unit 1
|
Determination
of density and viscosity of liquids
|
|
Unit 2
|
Distribution
of I2 between CCI4 and acqueous KI solution and calculation of formation
constant of KI3
|
|
Unit 3
|
Adsorption
of acetic acid on activated charcoal and Verification of Freundlion
adsorption isotherm
|
|
BLOCK 2
|
KINETIC STURY
|
|
Unit 4
|
Kinetics
of acids catalyzed hydrolysis of methyl acetate
|
|
Unit 5
|
kinetics
of Persulphate – Iodide reaction
|
|
BLOCK 3
|
CONDUCTIVITY STUDY
|
|
Unit 6
|
1.
Titration of strong acid with strong base
2.
Titration of weak acid with strong base
3.
Titration of mixture of acids with strong base
|
|
Unit 7
|
1.
Determination of cell constant
2.
Determination of solubility product
3.
Determination of dissociation constant of acetic
acid
|
|
BLOCK 4
|
POTENTIOMETRY
|
|
Unit 8
|
1.
Titration of strong acid with strong base
2.
Titration of weak acid with strong base
|
|
Unit 9
|
1.
Redox titration of Fe2+ with KMno4
2.
Single electrode Potential of Cu/Cu2+
|
|
BLOCK 5
|
PH METRY
|
|
Unit 10
|
1.
Measurement of PH of the given solution
2.
Preparation of buffers
3.
Determmination of PKa of weak acid
|
|
BLOCK 6
|
COLORIMETRY
|
|
Unit 11
|
Verification
of Lambert-Beer’s Law
|
|
BLOCK 7
|
POLARIMETRY
|
|
Unit 12
|
Determination of specific rotation of
Sucrose
Study of kinetics of acid catalysed
hydrolysis of Sucrose
|
|
CHE508
|
SPECTROSCOPY, COMPUTERS AND MATHEMATICS/
BIOLOGY
|
|
|
BLOCK 1
|
ABSORPTION SPECTROSCOPY
|
|
Unit 1
|
Infrared Spectroscopy
|
|
Unit 2
|
Analysis of the I.R. Spectra Problems
|
|
Unit 3
|
Proton Magnetic Resonance Spectroscopy
|
|
Unit 4
|
Analysis of 1HNMR spectrum problem
|
|
Unit 5
|
ultraviolet – visible spectroscopy
|
|
Unit 6
|
Mass Spectroscopy
|
|
Unit 7
|
Analysis of Mass Spectra Problems
|
|
Unit 8
|
Structural determination of organic compounds using the
Combined spectral data
|
|
BLOCK 2
|
COMPOUND APPLICATION IN CHEMISTRY PRACTICALS
|
|
Unit 9
|
Basic Language Practicals
|
|
Unit 10
|
C Language Practicals
|
Syllabus B.Sc. I, II & III
Chemistry Syllabus B.Sc. Programme (jlk;u foKku)
BSCCH12 B.Sc. First Year
Course
I- Inorganic Chemistry (CH01) Credit 03
(izFke iz”u i= % vdkcZfud
jlk;u ¼lh,p&01½
vf/kdre vad 50 le; 3 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
1 vk;fud Bksl % Hkkx&I
2 vk;fud Bksl % Hkkx&II
3 lgla;kstd cU/k&I % la;kstdrk cU/k fl)kUr
4 lgla;kstd cU/k&II % bysDVªWku U;wu ;kSfxdksa o
/kkrqvks esa cU/ku
5 lgla;kstd cU/k&III % v.kq d{kd fl)kUr
6 f}/kzqo vk?kw.kZ
7 s&CykWd rRo & I
8 s&CykWd rRo & II
9 p&CykWd rRoksa ds xq.kksa dh
vkorZrk & I
10 p&CykWd rRoksa ds xq.kksa dh
vkorZrk & II
11 p&CykWd rRoksa ds ;kSfxd
12 Qqyjhuksa] dkckZbMksa vkSj QyqvksjksdkcZuksa dk jlk;u
13 flfydsV] VsVªklYQj] VsVªkukbVªkbM
14 vUrj gSykstu ;kSfxd ,oa ikWyh gSykbM
15 mR—’V xSlsa
Course
II-Organic Chemistry (CH02) Credit
03
( f}rh; iz”u i= % dkcZfud
jlk;u ¼lh,p&02½
vf/kdre vad 50 le; 3 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
1 dkcZfud vfHkfØ;kvksa dh lkekU; /kkj.kk &I
2 dkcZfud vfHkfØ;kvksa dh lkekU; /kkj.kk &II
3 f=foe jlk;u fokKku &I
4 f=foe jlk;u fokKku &II
5 f=foe jlk;u fokKku III: T;kferh; leko;ork
6 f=foe jlk;u fokKku &IV : la:ih;
leko;ork
7 ,sYdsu ,oa pØh; ,sYdsu I
8 ,sYdhu ,oa pØh; ,sYdhsu II
9 ,sYdhu ,oa pØh; ,sYdhsu& III
10 MkbbZu
11 ,Ydkbu
12 ,sjhu ,oa ,sjkseSfVdrk
13 ,sjkseSfVd bysDVªkWuLusgh izfrLFkkiu
14 ,sfYdy ,oa ,sfjy gSykbM~l & I
15 ,sfYdy ,oa ,sfjy gSykbM~l & II
Course
III-Physical Chemistry (CH03)
Credit 03
r`rh; iz”u i= % HkkSfrd jlk;u ¼lh,p&03½
vf/kdre vad 50 le; 3 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
1 xf.kfr; ladYiuk,¡ ¼v½
2 xf.kfr; ladYiuk,¡ ¼c½
3 dEI;wVj ¼v½
4 dEI;wVj ¼c½
5 xSlh; voLFkk % Hkkx&I ¼vkn”kZ
xSlsa½
6 xSlh; voLFkk % Hkkx&II ¼okLrfod
xSlsa½
7 nzo voLFkk
8 Bksl voLFkk
9 fØLVy }kjk X&fdj.kksa dk
foorZu
10 dksyk;Mh voLFkk
11 Bkslksa esa nzo&tsy
12 jklk;fud cyxfrdh Hkkx &I
13 jklk;fud
cyxfrdh Hkkx & II
14 jklk;fud
cyxfrdh Hkkx & III
15 jklk;fud cyxfrdh Hkkx & IV
Course
IV(CH04) Practical Chemistry
izk;ksfxd iz”u i= % izk;ksfxd jlk;u ¼lh,p&04½
vf/kdre vad 50 le; 4 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
Hkkx I
% vdkcZfud jlk;u
1 xq.kkRed ifj{k.k % ewyHkwr vo/kkj.kk,¡
2 vEyh; ewydksa ¼_.kk;uksa½ dk Øec) xq.kkRed fo”ys’k.k
3 {kkjdh; ewydksa ¼/kuk;uksa½ dk “kq’d ifj{k.k
4 {kkjdh; ewydksa dk vknzZ ifj{k.k ds vuqlkj oxhZdj.k o
muds vknzZ ijh{k.k
Hkkx II
% dkcZfud jlk;u
5 iz;ksx”kkyk rduhd
6 rRoksa dk ijh{k.k
7 fØ;kRed lewgksa das ijh{k.k
8 dkcZfud ;kSfxdksa dk fof”k’V ijh{k.kksa
}kjk vfHkfu/kkZj.k ,oa
muds laHkkfor O;qRiUu
9 i`’B ruko
10 foLdkflrk
11 jklk;fud cyxfrdh
12 forj.k xq.kkad
Course
VII(CH07) Physical Chemistry
Credit 03
r`rh; iz”u i= % HkkSfrd jlk;u ¼lh,p&07½
vf/kdre vad 50 le; 3 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
1 Å’ekxfrdh Hkkx & I
2 Å’ekxfrdh Hkkx & II
3 Å’ekxfrdh Hkkx & III
4 Å’ekxfrdh Hkkx & IV
5 Å’ekxfrdh Hkkx & V
6 Å’ekxfrdh Hkkx & VI
7 jlk;fud lkE;
8 izkoLFkk dk fu;e Hkkx &I
9 izkoLFkk fu;e Hkkx & II
10 izkoLFkk fu;e Hkkx & III
11 oS/kqr jlk;u Hkkx &I
12 oS/kqr jlk;u Hkkx & II
13 oS/kqr jlk;u Hkkx & III
14 oS/kqr jlk;u Hkkx & IV
15 oS/kqr jlk;u Hkkx & V
Course
VIII (CH08) Physical Chemistry
izk;ksfxd iz”u i= % izk;ksfxd jlk;u ¼lh,p&08½
vf/kdre vad 50 le; 4 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
1 midj.ksa dk va”kkadu ,oa ekud foy;uksa dks cukus dh fof/k;k¡
2 vk;rukRed fo”ys’k.k % vEy&{kkj vuqekiu
3 vk;ruh fo”ys’k.k % jsMkWDl ,oa ladqyferh; vuqekiu
4 HkkjkRed fo”ys’k.k
5 iryh ijr ØkseSVksxzkQh
6 isij ØkseSVksxzkQh
7 xq.kkRed fo”ys’k.k % dkcZfud ;kSfxdksa ds fof”k’V ijh{k.k&I
8 xq.kkRed fo”ys’k.k % dkcZfud ;kSfxdksa ds fof”k’V ifj{k.k&II
9 O;qRiUuksa dk fojpu
10 laØe.k rki
11 izkoLFkk lkE;
12 Å’ek jlk;u
Syllabus Chemistry B.Sc. IIed
year
CHEMISTRY रसायन विज्ञान
|
CH-05
|
सीएच 05 Credit 03
|
|||
|
INORGANIC CHEMISTRY
|
अकार्बनिक रसायन
|
|||
|
Unit 1
|
The
element of first transition series
|
इकाई 1
|
प्रथम संक्रमण
श्रेणी के
तत्वों का
रसायन
|
|
|
Unit 2
|
The
element of second transition series
|
इकाई 2
|
द्वितीय संक्रमण
श्रेणी के
तत्वों का
रसायन
|
|
|
Unit 3
|
The
element of third transition series
|
इकाई 3
|
तृतीय संक्रमण
श्रेणी के
तत्वों का
रसायन
|
|
|
Unit 4
|
Oxidation and reduction - I
|
इकाई 4
|
ऑक्सीकरण और
अपचयन – I
|
|
|
Unit 5
|
Oxidation and reduction - II
|
इकाई 5
|
ऑक्सीकरण और
अपचयन – II
|
|
|
Unit 6
|
Co-ordinate compounds - I
|
इकाई 6
|
उपसहसंयोजक यौगिक
– I
|
|
|
Unit 7
|
Co-ordinate compounds - II
|
इकाई 7
|
उपसहसंयोजक यौगिक
– II
|
|
|
Unit 8
|
Chemistry of Lanthenaid series Elements - I
|
इकाई 8
|
लैन्थेनाइड तत्वों
का रसायन
– I
|
|
|
Unit 9
|
Chemistry of Lanthenaid series Elements - II
|
इकाई 9
|
लैन्थेनाइड तत्वों
का रसायन
– II
|
|
|
Unit 10
|
Chemistry
of Actinaid Series Elements -I
|
इकाई 10
|
ऐक्टिनाइड तत्वों
का रसायन
– I
|
|
|
Unit 11
|
Chemistry
of Actinaid Series Elements -II
|
इकाई 11
|
ऐक्टिनाइड तत्वों
का रसायन
– II
|
|
|
Unit 12
|
Acid and base
|
इकाई 12
|
अम्ल तथा
क्षारक
|
|
|
Unit 13
|
Anhydrous solvent - I
|
इकाई 13
|
निर्जल विलायक
– I
|
|
|
Unit 14
|
Anhydrous solvent – II
|
इकाई 14
|
निर्जल विलायक
– II
|
|
|
Unit 15
|
Anhydrous solvent - II
|
इकाई 15
|
निर्जल विलायक
– III
|
|
|
CH-06
|
सीएच 06 Credit 03
|
|||
|
ORGANIC CHEMISTRY
|
कार्बनिक रसायन
|
|||
|
Unit 1
|
Spectrometry-
I
|
इकाई 1
|
स्पेक्ट्रमिकी – I
|
|
|
Unit 2
|
Spectrometry-
II
|
इकाई 2
|
स्पेक्ट्रमिकी –II
|
|
|
Unit 3
|
Alcohol- I
|
इकाई 3
|
ऐल्कोहॉल – I
|
|
|
Unit 4
|
Alcohol-
II
|
इकाई 4
|
ऐल्कोहॉल – II
|
|
|
Unit 5
|
Phenol
|
इकाई 5
|
फीनॉल
|
|
|
Unit 6
|
Ether and
Epoxide
|
इकाई 6
|
ईथर एवं
इपॉक्साइड
|
|
|
Unit 7
|
Aldehyde and Ketones- I
|
इकाई 7
|
ऐल्डिहाइड एवं
कीटोन – I
|
|
|
Unit 8
|
Aldehyde and Ketones- II
|
इकाई 8
|
ऐल्डिहाइड एवं
कीटोन – II
|
|
|
Unit 9
|
Aldehyde and Ketones- III
|
इकाई 9
|
ऐल्डिहाइड एवं
कीटोन – III
|
|
|
Unit 10
|
Carboxylic
acid- I
|
इकाई 10
|
कार्बोक्सिलिक अम्ल
– I
|
|
|
Unit 11
|
Carboxylic acid- II
|
इकाई 11
|
कार्बोक्सिलिक अम्ल
– II
|
|
|
Unit 12
|
Carboxylic
acid- IIII
|
इकाई 12
|
कार्बोक्सिलिक अम्ल
- III (अम्ल
व्युत्पन्न)
|
|
|
Unit 13
|
Nitro compounds
|
इकाई 13
|
नाइट्रोयौगिक
|
|
|
Unit 14
|
Amenes
|
इकाई 14
|
ऐमीन
|
|
|
Unit 15
|
Diazonium
salts
|
इकाई 15
|
डाइजोनियम लवण
|
|
|
CH-07
|
सीएच 07
|
|||
|
PHYSICAL CHEMISTRY
|
भौतिक रसायन
|
|||
|
Unit 1
|
Thermodynamics
Part - I
|
इकाई 1
|
ऊष्मागतिकी भाग
– I
|
|
|
Unit 2
|
Thermodynamics Part-II
|
इकाई 2
|
ऊष्मागतिकी भाग
–II
|
|
|
Unit 3
|
Thermodynamics Part - III
|
इकाई 3
|
ऊष्मागतिकी भाग
– III
|
|
|
Unit 4
|
Thermodynamics part - IV
|
इकाई 4
|
ऊष्मागतिकी भाग
– IV
|
|
|
Unit 5
|
Thermodynamics Part - V
|
इकाई 5
|
ऊष्मागतिकी भाग
– V
|
|
|
Unit 6
|
Thermodynamics Part - VI
|
इकाई 6
|
ऊष्मागतिकी भाग
– VI
|
|
|
Unit 7
|
Chemical equilibrium
|
इकाई 7
|
रसायनिक साम्य
|
|
|
Unit 8
|
Phase
Rules -I
|
इकाई 8
|
प्रावस्था का
नियम भाग
–I
|
|
|
Unit 9
|
Phase
Rules -II
|
इकाई 9
|
प्रावस्था नियम
भाग – II
|
|
|
Unit 10
|
Phase
Rules -III
|
इकाई 10
|
प्रावस्था नियम
भाग – III
|
|
|
Unit 11
|
Electro-chemistry Part - I
|
इकाई 11
|
वैधुत रसायन
भाग – I
|
|
|
Unit 12
|
Electro-chemistry
Part – II
|
इकाई 12
|
वैधुत रसायन
भाग – II
|
|
|
Unit 13
|
Electro-chemistry
Part – III
|
इकाई 13
|
वैधुत रसायन
भाग – III
|
|
|
Unit 14
|
Electro-chemistry
Part – IV
|
इकाई 14
|
वैधुत रसायन
भाग – IV
|
|
|
Unit 15
|
Electro-chemistry
Part – V
|
इकाई 15
|
वैधुत रसायन
भाग - V
|
|
|
CH-08
|
सीएच
08 Credit 03
|
||
|
PRACTICAL
CHEMISTRY
|
प्रायोगिक
रसायन
|
||
|
Unit 1
|
Methods of
instrument calibration and preparation of standard solutions
|
इकाई
1
|
उपकरणें
का अंशांकन
एवं मानक
विलयनों को
बनाने की
विधियाँ
|
|
Unit 2
|
Volumetric anylysis: acid - base titration
|
इकाई
2
|
आयतनात्मक
विश्लेषण: अम्ल-क्षार
अनुमापन
|
|
Unit 3
|
Volumetric anylysis: redox titration
|
इकाई
3
|
आयतनी
विश्लेषण: रेडॉक्स
एवं संकुलमितीय
अनुमापन
|
|
Unit 4
|
Weight analysis
|
इकाई
4
|
भारात्मक
विश्लेषण
|
|
Unit 5
|
Thin layer chromatography
|
इकाई
5
|
पतली
परत क्रोमैटोग्राफी
|
|
Unit 6
|
Paper Chromatography
|
इकाई
6
|
पेपर
क्रोमैटोग्राफी
|
|
Unit 7
|
Qualitative analysis: typical tests of
organic compounds -I
|
इकाई
7
|
गुणात्मक
विश्लेषण: कार्बनिक
यौगिकों के
विशिष्ट परीक्षण-I
|
|
Unit 8
|
Qualitative
analysis: typical tests of organic compounds -II
|
इकाई
8
|
गुणात्मक
विश्लेषण: कार्बनिक
यौगिकों के
विशिष्ट परिक्षण-II
|
|
Unit 9
|
Derivatives ******
|
इकाई
9
|
व्युत्पन्नों
का विरचन
|
|
Unit 10
|
Transition temperature
|
इकाई
10
|
संक्रमण
ताप
|
|
Unit 11
|
Phase equilibrium
|
इकाई
11
|
प्रावस्था
साम्य
|
|
Unit 12
|
Thermal chemistry
|
इकाई
12
|
ऊष्मा
रसायन
|
ch-,llh- Hkkx r`rh;
BSCCH12
Course
IX(CH09) Inorganic Chemistry
Credit 03
izFke iz”u i= % vdkcZfud jlk;u ¼lh,p&09½
vf/kdre vad 50 le; 3 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
1 dBksj ,ao e`nq vEy rFkk {kkjd &I
2 dBksj ,ao e`nq vEy rFkk {kkjd &II
3 laØe.k /kkrq ladqyksa esa /kkrq&fyxs.M cU/ku&I
4 laØe.k /kkrq ladqyksa esa /kkrq&fyxs.M cU/ku&II
5 laØe.k /kkrq ladqyksa ds pqEcdh; xq.k&I
6 laØe.k /kkrq ladqyksa ds pqEcdh; xq.k&II
7 laØe.k /kkrq ladqyksa ds bysDVªkWu LisDVªkW&I
8 laØe.k /kkrq ladqyksa ds bysDVªkWu LisDVªkW&II
9 /kkrq ladqyksa ds Å’ekxfrdh; ,ao xfrdh; i{k
10 dkcZ/kkfRod jlk;u&I
11 dkcZ/kkfRod jlk;u&II
12 dkcZ/kkfRod jlk;u&II
13 tSo vdkcZfud jlk;u
14 flfydkWu
15 QkWLQsthUl
Course
X(CH10) Physical Chemistry
Credit 03
f}rh; iz”u i= % dkcZfud jlk;u ¼lh,p&10½
vf/kdre vad 50 le; 3 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
1 LisDVªksLdksih&I
2 LisDVªksLdksih&II
3 dkcZ/kkfRod ;kSfxd
4 dkcZlYQj ;kSfxd
5 gsVªkslkbZfDyd&I
6 gsVªkslkbZfDyd&II
7 bZuksysV }kjk dkcZfud la”ys’k.k
8 dkcksZgkbMªsV&I
9 dkcksZgkbMªsV&II
10 ,sehuks vEy
11 isIVkbM ,ao izksVhu
12 U;wfDyd vEy
13 olk]rsy ,ao viektZd
14 la”ysf’kr cgqyd
15 la”ysf’kr jatd
Course
XI(CH11) Physical Chemistry
r`rh; iz”u i= % HkkSfrd jlk;u ¼lh,p&11½
vf/kdre vad 50 le; 3 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
1 DokVe ;kfU=dh ¼Hkkx&I½
2 DokVe ;kfU=dh ¼Hkkx&II½
3 DokVe ;kfU=dh ¼Hkkx&III½
4 DokVe ;kfU=dh ¼Hkkx&IV½
5 DokVe ;kfU=dh ¼Hkkx&V½
6 LisDVªfedh ¼Hkkx&I½
7 LisDVªfedh ¼Hkkx&II½
8 LisDVªfedh ¼Hkkx&III½
9 izdk”k jlk;u ¼Hkkx & I½
10 izdk”k jlk;u ¼Hkkx & II½
11 HkkSfrd xq.k ,ao vkf.od lajpuk ¼Hkkx & I½
12 HkkSfrd xq.k ,ao vkf.od lajpuk ¼Hkkx & II½
13 foy;u]ruq foy;u rFkk v.kqla[; xq.k ¼Hkkx&I½
14 foy;u]ruq foy;u rFkk v.kqla[; xq.k ¼Hkkx & II½
15 foy;u]ruq foy;u rFkk v.kqla[; xq.k ¼Hkkx & III ½
Course
XII(CH12) Practical Chemistry Credit 03
izk;ksfxd iz”u i= % izk;ksfxd jlk;u ¼lh,p&12½
vf/kdre vad 50 le; 4 ?k.Vs U;wure mÙkh.kkZad 18
bdkbZ la[;k bdkbZ dk “kh’kZd
1 fo”ys’k.k ,ao fojpu
2 foyk;d fu’d’kZ.k fof/k }kjk fu’d’kZ.k ,ao vkdyu
3 vk;u foue; fof/k }kjk dk i`FkDdj.k ,oa vkdyu
4 lkekU; iz;ksx”kkyk rduhfd;k¡
5 nks Bksl vo;o ;qDr dkcZfud feJ.k dk xq.kkRed fo”ys’k.k%
feJ.k dk i`FkDdhdj.k ,ao nksuksa vo;oksa dh igpku
6 O;qRiUuksa dk fojpu
7 dkcZfud ;kSfxdksa dk la”ys’k.k ;k cukuk
8 oS|qr jlk;u
9 viorZufefr ,ao /kzqo.kfefr
10 v.kqHkkj fu/kkZj.k
11 o.kZfefr
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