T Y B Sc Chemistry_1 Syllabus Mumbai University by munotes
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UNIVERSITY OF MUMBAI
Syllabus for sem V & VI
Program: B.Sc.
Course: CHEMISTRY
(Credit Based Semester and Grading System with
effect from the academic year 201 6–2017)
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T.Y.B.Sc.
CHEMISTRY
Credit Based Semester and Gradin g System
To be implemented from the Academic year 201 6-2017
SEMESTER V
Theory
Course UNIT TOPICS Credits L / Week
1.1 Colligative Properties of Dilute
Solutions (8L)
1.1.1 Dilute solution, colligate
properties, Raou lt’s law, relative
lowering of vapour pressure.
1.1.2 Elevation in boiling point of a
solution, thermodynamic derivation
relating elevation in the boiling point
of a solution and the molar mass of the
non-volatile solute.
1.1.3 Depression in freezing point of a
solution, thermodynamic derivation
relating the depression in the freezing
point of a solution and the molar mass
of the non -volatile solute.
1.1.4 Osmotic pressure, van’t Hoff’s
equat ion for osmotic pressure,
(derivation is expected) and
USCH501 I determination of molar mass of the
2.5 1 solute. Abnormal molar masses of
solutes and van’t Hoff factor
(calculation of Degree of Association
and Degree of Dissociat ion.)
1.2 Phase Rule (7L)
1.2.1 Gibb’s phase rule and terms
involved in the equation.
1.2.2 Application of phase rule to ONE
component systems (i) water system,
(ii) sulphur system
1.2.3 Application of phase rule to
TWO component systems, condensed
systems, condens ed phase rule, eutectic
systems (Lead -Silver system),
desilverisation of lead.
1.2.4 Introduction to three component
system, explanation of phase diagram
for three liquids forming one
immiscible pair.
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2.1 Surface Chemistry & Catalysis
(9L)
2.1.1 Adsorption: Physical and
Chemical Adsorption, types of
adsorption isotherms . Langmuir’s
adsorption isotherm (Postulates and
derivation expected). B.E.T. equation
for multilayer adsorption, (derivation
not expected). significance of the terms
involved in the equation is
expected.),determination of surface
area of an adsorbent using B.E.T.
equation. Numericals on surface area
determination are expected.
2.1.2 Catalysis: Homogeneous and
heterogeneous catalysis, catalytic
activity and selectivity, promoters,
inhibitors, catal yst poisoning and
deactivation,
2.1.3 Acid -Base catalysis , mechanism
II and kinetics of acid -base catalyzed
reactions, effect of pH on acid -base
catalyzed reactions. Mechanism and
kinetics of enzyme catalyzed reaction
(Michaelis -Menten equation).
2.2 Colloids (6L)
2.2.1 Introduction to colloidal state of
matter.
2.2.2 Origin of charge on colloidal
particles. Concept of electrical double
layer, zeta potential, Helmholtz and
Stern model, Electro -kinetic
phenomena:1.Electrophoresis ,
2.Electrophoresis ,
3. Streaming potential
4. Sedimentation potential .
2.2.3 Colloidal electrolytes.
2.2.4 Donnan Membrane Equilibrium.
2.2.5 Surfactants, micelle formation,
applications of surfactants in
detergents, food industry, in pesticide
formulations.
3.1 Electrochemistry –
Electrochemical cells (15L)
3.1.1 Lewis concept of Activity and
Activity coefficient, Mean ionic
III activity and mean ionic activity
coefficient γ +- of an electrolyte,
expression for activities of electrolytes
of different valence type, ionic strength
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3.1.2 Classification of cells: 1.chemical
cells without transference
2.Concentration cells with and without
transference (derivations of
expression for concentration cell EMF
are expected) Origin of liquid -liquid
junction pot ential and its elimination
using a salt bridge.
3.1.3 Applications of EMF
.measurements in the determination
of 1. pH of a solution using
quinhydrone and glass electrode. 2
solubility and solubility product of
sparin gly soluble salts using chemical
cell and concentration cell method 3.
determination of liquid -liquid junction
potential .
4.1 Introduction to Polymers (8L)
4.1.1 Basic terms : macromolecule,
monomer, repeat unit, degree o f
polymerization.
4.1.2. Classification of polymers
based on (i) source, (ii) structure, (iii)
thermal response, (iv) physical
properties.
4.1.3. Molar masses of polymers : 1.
Number average molar mass, 2.Weight
average molar mass, 3. Viscosity
average molar mass, monodispersity,
polydispersity.
4.1.4. Methods of determining molar
masses of polymers : 1. Ultrcentrifuge
method ( Limiting velocity method
IV only). Viscosity meth od ( Mark - 1 Houwink equation).
4.1.5. Introduction to light emmiting
polymers ( characteristics, method of
preparation and it’s application are
expected ).
4.2 Crystalline State (7L)
4.2.1. Laws of Crystal lography
4.2.2 . Characteristics of simple cubic,
face centered and body centered cubic
system, inter planar distance in cubic
lattices ( only expressions for ratios of
inter planar distances are expected ).
4.2.3. Use of X- rays in the study of
crystal structure, Bragg’s equation (
derivation expected), X - ray diffraction
method of studying crystal lattices,
structure of NaCl and KCl,
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determination of Avagadro number.
4.2.4. Elementary idea of defects in
crystals - Frenkel defect and Schottky
defect.
1. Chemical Bonding And Solid State
Chemistry (15L)
1.1 Molecular Symmetry ( 7L)
1.1.1 Introduction and Importance.
1.1.2 Symmetry elements and
symmetry op erations.
1.1.3 Concept of a Point Group with
illustrations using the following point
USCH502 I gro ups: (i) C αv (HCl), (ii) D αh (H2),
2.5 1 (iii) C2v (H 2O), (iv) C 3v (NH 3), (v) C 2h
(trans – trichloroethylene), and (vi) D 3h
(BCl 3).
1.2 Molecular Orbital Theory for
Polyatomic Species (5L)
1.2.1 Simple triatomic species: H 3+ and
H3 (correlation between bond angle and
Molecular orbitals).
Term such as Walsh correlation diagram,
Symmetry Adapted Linear Combinations
(SALCs), Ligand Group orbitals (LGOs),
transformation of atomic orbitals into
appropriate symmetry types, exp ected to be
discussed
1.3 (3L)
Other molecules (considering
only σ-bonding): i) BeH 2, ii) H 2O,
Explanation of terms viz.crystal
lattice, lattice points, unit cells and
lattice constants.
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2. Solid Materials (15L)
2.1 Structures of Solids (10L)
2.1.1 Importance of solid state
chemistry.
2.1.2 Classificatio n of solids on the
basis of bonding.
2.1.3 Closest packing of rigid spheres
(hcp, ccp), packing density in simple
cubic, bcc, fcc and hcp lattices
(numerical problems expected).
Point defects with respect to Frenkel
and Schottky defects expected.
2.1.4 Structure metallic solids.
2.1.5 Tetrahedral and octahedral
interstitial voids in ccp lattice,
tetrahedral holes,limiting radius
ratios
II for different coordination numbers and
their significance, calculation of
limiting radius ratio for coordination
number 4.
2.1.7 Structures of sodium chloride and
cesium chloride. 2.2 Superconductivity (05L)
2.2.1 Superconductivity, Meissner
effect.
2.2.2 Different superconducting
materials viz,convential
superconductors, organic
superconductors, alkali metal fullerides
(A3C60) and hi gh temperature
Superconductors.
2.2.3 Applications of superconducting
materials .
3. Chemistry of elements (15L)
3.1 Inner transition elements (3L)
3.1.1 Introduction: position of f -block
elements and comparison between
lanthanides and actinides
3.1.2 The shapes of f-orbitals.
3.1 Lanthanides Series (10L)
III 3.2.1 Chemistry of lanthanides with
reference to (i) lanthanide contraction,
(ii) Oxidation states (iii) magnetic and
spectral properties, 3.2.2 Occurrence, extraction and
separation of lanthanides by Solvent
extraction. 3.2.3 Applications of lanthanides.
1
1
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3.3 Actinides Series (2L)
3.3.1 Chemistry of Uranium and with
reference to occurrence, extraction
(solvent extraction method),
3.3.2 Properties and applications.
4. Solution Chemistry
4.1 Acid -base Chemistry in Aqueous
Medium (8L)
4.1.1 Acidity of mono - and polyatomic
cations.
4.1.2 Basicity of mono - and polyatomic
anions (discussion for 4 .1.1 as well as
4.1.2 to Include Latimer equation and
IV predominance diagrams). 1 4.2 Chemistry in Non -aqueous
Solvents (7L)
4.2.1 Classification of solvents and
importance of non -aqueous solvents.
4.2.2 Characteristi cs and study of
liquid ammonia, dinitrogen tetraoxide
and acetic acid as non -aqueous
solvents with respect to (i) acid -base
reactions and (ii) redox reactions.
1.1. Mechanism of Organic
Reactions (15L)
1.1.1 Thermo dynamic and Kinetic
control of organic reactions: Concept
with mechanisms of the following
reactions: addition of HX to butadiene;
sulfonation of naphthalene.
Nucleophilicity/ electrophilicity vs
Basicity/acidity.
1.1.2 Mechanism of elimination
reactions, with stereochemistry: E1 and
E2 reactions: regioselectivity (Saytzeff
and Hofmann rules).
USCH503 I 1.1.3 Mechanism of reactions of 2.5 1 carbonyl compounds with
nucleophiles: 1.1.3.1 Formation of
acetals/ketals from aldehydes and
ketone s. 1.1.3.2 Reaction of aldehydes
and ketones with primary and
secondary amines. 1.1.3.3 Acyl
nucleophilic substitution (tetrahedral
mechanism): Acid catalysed
esterification of Carboxylic acids and
base promoted hydrolysis of esters.
1.1.4 Mechanism of rearrangements
with examples and stereochemistry
wherever applicable. 1.1.4.1 Migration
to electron deficient carbon: Pinacol,
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Benzylic acid. 1.1.4.2 Migration to
electron deficient nitrogen: Beckm ann,
Hofmann.
1.1.5 Mechanism of the following
reactons with synthetic application:
Claisen condensation, Michael
addition.
2. Stereochemistry (15L)
2.1.1 Molecular chirality and element
of symmetry: Mirror Plane symmetry
(inversion centre), rotation -reflection
(alternating) axis, Chirality of
compounds without stereogenic
centre: cummulenes, spirans and
biphenyls.
2.1.2 Stability ofcycloalkanes: Strains
in cycloalkanes -angle,eclipising,
transannu lar (3 to 8 membered).
Conformations of cyclohexane, mono -
and di - alkyl cyclohexanes and their
relative stabilities.
II 2.1.3 Stereo selectivity and Stereo
specificity: Idea of enantioselectivity
(ee) and diastereosele ctivity
(de).Topicity -enantiotopic and
diastereotopic atoms, groups and faces.
Stereochemistry of -
(1) Substitution reactions - SN1, S N2,
SNi (reaction of alcohol with thionyl
chloride). (2) E 2-anti-elimination -Base
induced dehydrohalogenation of 1 -
bromo -1,2- diphenylpropane.
(3) Addition reactions to olefins -i)
catalytic hydrogenation ii) bromination
(electrophilic anti addition) (iii)syn -
hydroxylation (molecular addition)
with OsO 4 and KM nO4.
3.1 Carbohydrates (10L)
3.1.1 Introduction: Classification,
Sources, Reducing and non -reducing
sugars DL notation.
3.1.2 Structures of monosaccharides:
Fischer projection (4 -6 carbon
III monosaccharides and Haworth
formula -Furanose and pyranose forms
of pentoses and hexoses.
Interconversion :open and Haworth
forms of monosaccharides with 5 and
6 carbons. Chair conformation with
stereochemistry of D -glucose and D -
fructose. St ability of chair forms of D -
1
1
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glucose.
3.1.3 Determination of open chain
configuration - of D-glucose assuming
the configuration of D -arabinose; and
of D-fructose assuming the
configuration of D -glucose.
3.1.4 Anomers and epimers of
monosaccharides. Enantiomers and
diastereomers of glucose. Mutarotation
(with mechanism) in D -glucose.
3.1.5 Chain lengthening and shortening
reaction: Modified kiliani -fischer
synthesis. Wohl method.
3.1.6 Reactions of D-glucose and D -
fructose: (a) osazone formation (b)
reduction - H2/Ni, NaBH 4 c)oxidation -
bromine water, HNO 3, HIO 4. D)
interconversion of D -glucose
and D -fructose e) acetylation f)
methylation [e and f with cyclic
pyranose form].
3.1.7 Commercial importance of
carbohydrates in pharmaceutical,
paper,food and Textile industries.
3.2. IUPAC Nomenclature (5L)
IUPAC systematic and accepted trivial
nomenclature of the following classes
of compounds, including substituted
ones (up to 2 substituents/ functional
group s):
3.2.1 (a)Bicyclic compounds - spiro -
,fused, and bridged (upto 11carbon
atoms) -saturated and unsaturated
compounds.
3.2.2 (b) Biphenyls.
3.2.3 (c) Cummulenes upto 3 double
bonds (d) Monocyclic (5 and 6
membered) aromatic and non -aromatic
heterocyclic compounds containing a
maximum of two hetero atoms among
N,O,S.
3.1.1 Introduction:Classification,
Sources, Reducing and non -reducing
sugars DL notation.
3.1.2 Structures of monosaccharides:
Fischer projection (4 - 6 carbon
monosaccharides and Haworth
formula -Furanose and pyrano se forms
of pentoses and hexoses.
Interconversion :open and Haworth
forms of monosaccharides with 5 and
6 carbons. Chair conformation with
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stereochemistry of D -glucose and D -
fructose. Stability of chair forms of D -
glucose.
3.1.3 Determ ination of open chain
configuration - of D-glucose assuming
the configuration of D -arabinose; and
of D-fructose assuming the
configuration of D -glucose.
3.1.4 Anomers and epimers of
monosaccharides. Enantiomers and
diast ereomers glucose. Mutarotation
(with mechanism) in D -glucose.
3.1.5 Chain lengthening and shortening
reaction: Modified kiliani -fischer
synthesis. Wohl method.
3.1.6 Reactions of D -glucose and D -
fructose: (a) osazone formati on (b)
reduction - H2/Ni, NaBH 4 c)oxidation -
bromine water, HNO 3, HIO 4. D)
interconversion of D -glucose
and D -fructose e) acetylation f)
methylation [e and f with cyclic
pyranose form].
3.2. IUPAC Nomenclature (5L)
IUPAC systematic and accepted trivial
nomenclature of the following classes
of compounds, including substituted
ones (up to 2 substituents/functional
groups):
3.2.1 (a)Bicyclic compounds - spiro -
,fused, and bridged (upto 11ca rbon
atoms) -saturated and unsaturated
compounds.
3.2.2 (b) Biphenyls.
3.2.3 (c) Cummulenes upto 3 double
bonds (d) Monocyclic (5 and 6
membered) aromatic and non -aromatic
heterocyclic compounds containing a
maximum of two hetero
atoms among N,O,S.
4.1. Heterocyclic Chemistry (8L)
4.1.1 Introduction: Electronic structure
and aromaticity of furan,
pyrrole,thiophene and pyridine.
IV 4.1.2 Synthesis: Synthesis of furans,
1 pyrroles, an d thiophenes by Paal -Knor
synthesis. Pyridines by Hantzsch
synthesis and from 1,5 -diketones.
4.1.3 Reactivity: Reactivity towards
electrophilic substitution reactions - of
furan, pyrrole and thiophene on basis
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of stability of intermediate; and of
pyridine on the basis of electron
distribution.Nucleophilic substitution
reaction of pyridine on the basis of
electron distribution.
4.1.4 Reactions of heterocycles: The
following reactions of furan, pyrrole
and thioph ene: Halogenation ,
Nitration, Sulphonation, Vilsmeir
formylation reaction, Friedel -Crafts
reaction. Furan: Diels -Alder reaction.
Ring opening of furan. Pyrrole: Acidity
and basicity of pyrrole -Comparison of
basicity of pyrrole and
pyrrolidine, Acid cata lyzed
polymerization of pyrrole. Pyridine:
Basicity. Comparison of basicity of
pyridine, pyrrole and piperidine.
Sulphonation of pyridine, with and
without catalyst. Reduction.Oxidation
of alkyl pyridines and action of
sodamide (Chichibabin reaction).N -
methylation of pyridine. Quaternization
of piperdine, pyrrolidine and Hofmann
elimination of the quaternary salts.
4.2. Organic Synthesis (7L)
4.2.1 Introduction: Criteria for ideal
organic synthesis. Yield and
selectivity. Multi - component synthesis
– with example s, Mannich reaction,
Hanztsch synthesis of
pyridines (without mechanism).
4.2.2 Illustrative synthesis of
industrially important compounds:
Ibuprofen (chiral synthesis),
paracetamol (green synthesis), L -
ascorbic acid (from D -glucose),
norfloxacin, thyroxine, van illin,
methyl dihydrojasmonate (Hedione),
Bifenox -I, pigment red 242, indigo, 2 -
hydroxy -3-amino -5-nitrobenzene
sulphonic acid.
4.2.3 Newer methods of organic
synthesis: Introduction to the use of the
following in organic synthesis:
Ultrasound, microwaves, PTC.
4.1.1 Introduction: aromaticity of
furan,pyrrole,thiophene and
pyridine.
4.1.2 Synthesis: Synthesis of furans,
pyrroles, and thiophenes by Paal -Knor
synthesis. Pyridines by Hantzsch
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synthesis and from 1,5 -diketones. 4.1.3
Reactivity: Reactivity towards
electrophilic s ubstitution reactions - of
furan, pyrrole and thiophene on basis
of stability of intermediate; and of
pyridine on the basis of electron
distribution. Nucleophilic substitution
reaction of pyridine on the basis of
electron distribution.
4.1.4 Reactions of heterocycles: The
following reactions of furan, pyrrole
and thiophene: Vilsmeir formylation
reaction, Friedel -Crafts reaction.
Furan: Diels -Alder reaction. Ring
opening of furan. Pyrrole: Acidity and
basicity of pyrrole -Comparison of
basicity o f pyrrole and pyrrolidine,
Acid catalyzed polymerization of
pyrrole. Pyridine: Basicity.
Comparison of basicity of pyridine,
pyrrole and piperidine. Sulphonation
of pyridine, with and without catalyst.
Reduction.Oxidation of alkyl
pyridines and action of s odamide
(Chichibabin reaction). N -methylation
of pyridine.Quaternization of
piperdine, pyrrolidine and Hofmann
elimination of the quaternary salts.
4.2. Organic Synthesis (7L)
4.2.1 Introduction: Criteria for ideal
organic synthesis. Yield and
selectivity. Multi - component
synthesis – with examples, Mannich
reaction, Hanztsch synthesis of
pyridines (without mechanism).
4.2.2 Illustrative synthesis of
industrially important compounds:
Ibuprofen (chiral synthesis),
paracetamol (green synthesis), L -
ascorbic acid (from D -glucose),
norfloxacin, nalidixic acid, vanillin,
methyl dihydrojasmonate (Hedione),
Bifenox -I, pigment red 242, 2 -
hydroxy -3-amino -5-nitrobenzene
sulphonic acid.
4.2.3 Newer methods of organic
synthesis: Introduction to the use of
the following in organic synthesi s:
Ultrasound, microwaves, PTC.
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1. Treatment of analytical data -I and
sampling (15 L)
1.1 Treatment of Analytical Data
(7L)
Types of errors, determinate and
indeterminate errors, minimization of
errors, constant and propo rtionate
errors, accuracy and precision,
measures of dispersion and central
tendency: mean, median, average
deviation, relative average deviation,
standard deviation, variance,
coefficient of variation.[Numerical
I problem s expected] 1 1.2 Sampling (8L)
Terms involved, importance of
sampling, sampling techniques,
sampling of gases, ambient and stack
sampling, equipment used, sampling of
homogeneous and heterogeneous
liquids, sam pling of static and flowing
liquids, methods and equipments used,
sampling of solids, importance of
particle size and sample size, samples
used, need for the reduction in the
USCH504 sample size, methods of reduction in 2.5
samp le size, collection, preservation
and dissolution of the sample.
2. Titrimetric analysis -I and UV -
Visible spectroscopy. (15L)
2.1 Acid -base Titrations (5L)
Construction of titration curves and
choice of indicators in th e titration of
[1] strong acid and strong base, [2]
strong acid and weak base, [3] weak
acid and strong base, [4] weak acid and
weak base.
2.2 Precipitation titrations (4L)
II Argentimetric titrations, construction
1 of the titration curve, Volhard’s
method, Mohr’s method, adsorption
indicators, theory and applications .
2.3 U.V. Visible Spectroscopy (4L)
Photometers and spectrophotometers,
Instrumentation in the case of single
and doubl e beam spectrophotometers,
Qualitative and quantitative analysis,
calibration cure method.
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3. Methods of separation -I (15L)
3.1 Solvent Extraction (8L)
Partition coefficient and distribution
ratio, extraction efficiency, separation
factor, role of complexing agents in
solvent extraction, chelation, ion pair
formation, solvation, types of solvent
III extraction: batch, continuous.
1 [Numerical problems expected]
3.2 Chromatography (2 L)
Introduction to chromatographic
techniques, classification of
chromatographic techniques.
3.3 Planar Chromatography (5L)
Principle, techniques and applications
of [1] Paper chromatography [2] Thin
layer chromatography
4. Optical methods (15L)
4.1 Atomic Spectroscopy (7L)
Absorption and emission spectra,
energy level diagrams, process
involved in atomization, flame
photometry, flame atomizer, types of
burners, monochromators and
detectors, atomic absorption
spectroscopy; flame and electrothermal
atomizer, sources, instrumentation,
quantitative applications of atomic
absorption and flame photometry,
IV calibration curve method, standard
1 addition and internal standard method.
4.2 Molecular Fluorescence and
Phosphorescence Spectroscopy (4L)
Theory, instrumentation and
applications
4.3 Turbidimetry and Nephelometry
(4L)
Scattering of light, effect of
concentr ation, particle size and
wavelength on light scattering,
instrumentation and applications.
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Practicals
Practicals of Course USCH501
Physical Practicals
Chemical Kinetics –
To determine the order between K 2S2O8 & KI
by fractional change method.
Viscosity –
To determine the molecular weight of high
polymer polyvinyl alcohol (PVA) by
viscosity measurement.
OR
To determine the radius of a glycerol
molecule by viscosity measurement.
Potentiometry –
1. To determine the amount of Fe(II) in the
given solution by titration with a
standard K 2Cr2O7 solution and hence to
find the formal redox potential of
Fe3+/Fe2+
2. To determine the solubility product and
solubility of AgCl potentiometrically
USCHP05 using chemical cell. 3 8
OR
3. To determine the solubility product and
solubility of AgCl potentiometrically
using concentration cell.
Colorimetry –
To determine the amount of Fe(III) present
in the given solution by using salicylic acid
by colorimetric titration.(static method)
( =525 nm)
pH –Metry –
To determine acidic and basic dissociation
constants of amino acid hence to calculate
isoelectric point.
Course USCH502
Inorganic Practicals
Inorganic preparations
1. Potassium diaquo bis -
(oxalate)cuprate
(II)K 2[Cu(C 2O4)2.(H 2O]
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2. CuCl2 -2DMSO
3. Bis(ethylene
diamine)iron(II)sulphate[C 2H4(
NH 2)2FeSO 4.4H 2O].
4. Skill based Qualita tive
preparation of Chromium
(II)acetate Cr(OAc) 2 so that the
following outcomes are
achieved:
Setting up reactor for Cr(II)
ions
Identification of oxidation
states of Chromium
Preparation of
chromium(II)acetate
Isolation of the product
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Volumetric analysis
1. Determination of
magnesium from
the supplied
commercial sample
of Milk of magnesia
tablet
2. Estimation of Nickel(II) complexome -
trically using murexide indicator
(Students are expected to standardize
supplied EDTA solut ion using ZnSO 4.7H 20)
Practicals of Course USCH503
Organic Practicals
i. Separation of binary (solid -slid)
mixture.(Weights and physical constant of both
crude components of the mixture are to be
reported. (Minimum 4 mixtures)
ii. Identification of an organic compound of
known chemical type. (Minimum 4 mixtures)
Syllabus for Organic Chemistry Sem -VI
Organic preparations
i. Acetylation of hydroquinone.
ii. Nitration of nitrobenzene.
iii. Hydrolysis of ethyl benzoate.
iv. Bromination of acetanilid e.
Course USCH504
Analytical Practicals
1. Estimation of persulphate in the given
sample by the method of back
titration.
USCHP06 2. Determination of the calcium and the 3 8 magnesium content of a dolomite
sample.
3. Determination of glucose content of a
honey sample by Wilstater’s method.
4. Determination of the amount of
fluoride in the given solution
colorimetrically.
5. Determination of Vitamin C content
of a given ta blet by titration with
sodium hydroxide pH metrically
Page 20
T.Y.B.Sc.
Chemistry
Credit Based Semester and Grading System
To be implemented from the Academic year 201 6-2017
SEMESTER VI
Theory
Course UNIT Credits L / Week
1.1 Molecul ar Spectroscopy –I (15L)
1.1.1 Dipole moment: Dipole moment,
polarization of a bond, bond moment,
dipole moment and molecular structure.
1.1.2 Rotational Spectrum: Rotational
spectrum of a diatomic molecule, rigid
rotor, moment of inertia, energy levels,
conditions for obtaining pure rotational
spectrum, selection rule, nature of
spectrum, determination of inter nuclear
distance and isotopic shift.
1.1.3 Vibration ( IR ) spectrum:
Vibrational motion, degrees of freedom,
modes of vibration, vibrational spectrum of
a diat omic molecule, simple harmonic
oscillator, energy levels, zero point energy,
conditions for obtaining vibrational
spectrum, selection rule, nature of
I spectrum. 1
1.1.4 Vibration -Rotation spectrum of
USCH601 diatomic molecule v ibrating rotor, energy
2.5 levels, selection rule, nature of spectrum, R
and P branches, anharmonic oscillator :
energy levels, selection rule, fundamental
band, overtones . Application of vibration -
rotation spectrum in determining Force
constant, determina tion and significance.
Introduction to infrared spectra of simple
molecules like H 2O and CO 2
1.1.5 Raman Spectroscopy : Scattering of
electromagnetic radiation, Rayleigh
scattering, Raman scattering, nature of
Raman spectrum , Stoke’s lines,anti -
Stoke’s lines, Raman shift, quantum theory
of Raman spectrum, comparative study of
IR and Raman spectra, rule of mutual
exclusion.(example of CO 2molecule).
2.1 Basics of Quantum Chemistry (10L)
II 2.1.1 Classical mechanics, limitations of
1 classical mechanics, Black body radiation,
photoelectric effect, Compton effect.
2.1.2 Introduction to quantum mechanics,
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Planck’s theory of quantization, wave
particle duality, de -Broglie equation,
Heisenberg’s uncertainty principle.
2.1.3 Progressive and standing waves,
boundary conditions, Schrodinger’s time
independent wave equation(derivation not
expected)., interpretation and properties of
wave function.
2.1.4 Postulates of quantum mechanics (
following a re to be considered),1. state
function and it’s significance2. Concept of
operators : definition, addition, subtraction
and multiplication of operators,
commutative and non - commutative
operators, linear operator, Hamiltonian
operator, 3. Eigen function and eigen value,
eigen value equation.
2.2 Applied Electrochemistry (5L)
2.2.1 Polarization, concentration
polarization and it’s elimination
2.2.2 Decomposition potential,
experimental determination of
decomposition potential, factors affecting
decomposition potential (nature of
electrolyte, nature of electrodes and
temperature) Tafel’s equation for hydrogen
overvoltage, Overvoltage, experimental
determination of over -voltage,
2.2.3
Electroplating ---objectives and procedures
3.1 Renewable Energy Sources (5L)
3.1.1. Lithium ion cell.
3.1.2 . Fuel cells; Choice of fuel and
oxidant, Bacon’s H 2 and O 2 fuel cell.
3.1.3 . Solar cells, solar e nergy, photovoltaic
effect, semiconductors as solar energy
converters, silicon solar cell
3.1.4 . Hydrogen : Fuel of the future,
production of hydrogen by direct
electrolysis of water, advantages of
III hydrogen as a universal e nergy medium. 1 3.2 Nuclear Magnetic Resonance
Spectroscopy (6L)
3.2.1 . Nuclear spin, magnetic moment,
nuclear ‘g’ factor, energy levels, Larmor
precession, Relaxation processes in n.m.r. (
spin-spin relaxation and spin -lattice
relaxation).
3.2.2 . NMR Spectrometer, chemical shift,
shielding and deshielding of protons, low
resolution n.m.r. spectrum of methanol and
ethanol.
Page 22
Page 23
3.3 Chemical Kinetics (4 L)
3.3.1 Collision theory of reacti on rates,
application of collision theory to 1. uni -
molecular reaction and 2. bimolecular
reaction ( Lindemann theory, derivation
expected). Merits and drawbacks of
collision theory.
3.3.2 Classification of reactions as slow,
fast and ultra -fast. stu dy of kinetics of fast
reactions by Stop flow method.
4.1 Nuclear Chemistry
4.1.1 Types of nuclear radiations and their
characteristics, behaviour of ion pairs in
electric field, detecton and measurement of
nuclear radiations using G. M. Counter
and Scintillation Counter.
4.1.2 Kinetics of radioactive decay, units of
radioactivity (Curie, Bequerel, Rutherford)
4.1.3 Radioactive equilibrium ( secular and
transient), determination of radioactive
constants for radio -elements having 1.
moderate half life, 2. long half life
IV 3.extremely long or short half life. 1 4.1.4 Use of radioisotpes as tracers in 1.
chemical investigations - reaction
mechanism, 2. age determination - dating by
carbon-14
4.1.5 Nuclear reactions – nuclear
transmutation, artificial radioactivity Q -
value of nuclear reaction, threshold energy.
4.1.6 Fissile and fertile material, nuclear
fission, chain reaction, factor controlling
fission process. ( multiplication factor and
critical size or mass of fissionable
material)., nuclear power reactor and
breeder reactor.
Coordination Chemistry (15L)
1.1 Crystal Field Theory (CFT)
1.1.1 Basic tenets of Crystal field theory
and effect of crystal field on central metal
valence orbitals .
1.1.2 Splitting of d orbitals in octahedral,
USCH602 I tetrahedral and square planar complexes. 2.5 1
1.1.3 Crystal field splitting energy
(10 / o) for octahedral complexes and
factors affecting the magnitude of
o.
1.1.4 Crystal field stabil ization energy
(CFSE), calculation of CFSE, for
octahedral and tetrahedral complexes with
Page 24
d1 to d10 metal ion configurations.
1.1.5 Effect of crystal field splitting on
i) Ionic radius and ii) Lattice energy.
1.1.6 Theoretical failure of the CFT model.
1.1.7 Experimental evidence for co -
valence in co -ordination compounds.(i)
ESR spectrum of [IrCl 6]2- (ii) NMR
spectrum of tris (acetyl acetanato)
vanadium complex, (iii) Intensities of d-d
transitions, and (iv) Nephelauxetic effect.
Consequences of crystal field sp litting on
various properties such as ionic radii,
hydration energy, lattice energy, enthalpies
of formation, colour and magnetic
properties.
1.2 Molecular Orbital Theory (MOT) of
Coordination Complexes
1.2.1 Application to octahedral complexes
in ca se of (i) [Ti(H 2O)]3+, (ii) Fluoro
complexes of Fe(II) and Fe (III) and (iii)
Cyano complexes of Fe(II) and Fe (III).
1.2.2 Effect of pi -bonding an ligand field
splitting parameter in M→L and L→M
interactions.
1.3 Electronic States and Terms for
Polyelectronic Atoms
1.3.1 Introduction: electronic
configuration and electronic states, Term
symbols, coupling of spin momenta
(Ms),orbital momenta (M l)and spin - orbit
coupling or Russell -Saunders coupling.
1.3.2 Determination of Terms for p2
electronic configuration (as in a
carbon atom).
1.3.3 Terms and micro -states for transition
metal atoms/ions.
2. Properties of Coordination compounds
(15L)
2.1 Stability of Complexes (5L)
2.1.1 Thermodynamic stability and kinetic
stability of complexes with examples.
2.1.2 Stability constants: Stepwise and
overall constants and their inter -
relationship.
2.1.3 Factors affecting thermodynamic
II stability. 1 2.1.4 Potentiometric method of
determination of stability constants with
example of silver -ammon ia complex.
2.2 Substitution Reactions in Octahedral
Complexes (5L)
Page 25
2.2.1 Introduction, types of reactions in
complexes.
2.2.2 Ligand substitution reactions: basic
mechanisms.
2.2.3 Inert and labile complexes and
Page 26
electronic configurations and lability of
complexes.
2.2.4 Acid hydrolysis, base hydrolysis and
anation reactions.
2.3 Electronic Spectra (5L)
2.3.1 Types of electronic transitions like
intra –ligand transitions, charge transfer
transitions and intra -metal transitions and
(d-d or ligand field tr ansitions for
transition metals).
2.3.2 Rules for electronic transitions: Spin
and Orbital or Laporte selection rules.
Orgel Diagrams for D Terms (i.e, d1 , d4 and
d6 .d9 electronic configurations) and its use
in interpretation of visible electronic
absorption spectra of these configurations.
Organometallic Chemistry (15L)
3.1 Organometallic Compounds of main
group metals (6L)
3.1.1 Introduction: General synthetic
methods: (i) Oxidative addition, (ii) Metal -
Metal exchange (Transmetallation), (iii)
Carbanion -Halide exchange, (iv) Metal
Hydrogen exchange and (v) Methylene
insertion reactions.
3.1.2 Chemical rections: (i) Reactions with
oxygen, (ii) Alkylation and arylation
reactions (iii) Reactions with protic
reagents and (iv) Complex formation
III reaction s.
3.2 Organometallic compounds of
transition metals (9L)
3.2.1 Synthesis , structure, reactions and of
ferrocene.
3.2.2 Bonding in ferrocene on the basis of
VBT.
3.2.3 Bonding in Re and Mo halide
complexes.
Some Selected Topics (15L)
4.1 Inorganic Polymers (3L)
4.1.1Vari ous methods of classification with
examples. IV 4.1.2 Chemistry of borazine with reference
to preparation , properties, structures,
bonding and applications.
4.2 Characteristics and Treatment
1
1
Page 27
of Liquid Effluent (06L)
4.2.2 Characterization of waste:
biochemical oxygen demand (BOD),
chemical oxygen demand (COD), total
organic carbon (TOC), aerobic and
anaerobic processes.
4.2.3 Removing of solid
contaminants, physical and chemical
principles such as coagulation, flocculation
and sedimentation.
4.2.4 Primary,secondary and
tertiary of liquid effluents.
4.3 Nanomaterials(04L)
4.3.2 Introduction and importance
of nanomaterials.
4.3.3 Properties (Comparison
between bulk and nanomaterials): (i)
Optical proper ties, (ii) Electrical
conductivity, and (iii) Mechanical
properties.
4.3.4 Forms of nanomaterials:
nanofilms, nanolayers, nanotubes,
nanowires, and nanoparticles.
4.3.5 Chemical methods of
preparation: (i) Colloidal route, and (ii) Sol -
gel method.
4.5 Inorganic Pharm aceuticals (2L)
4.4.2 Gastrointestinal agents viz.,
(i) antacids (aluminium hydroxide, milk of
magnesia, sodium bicarbonate and (ii)
cathartics (magnesium sulphate and sodium
phosphate).
Topical agents viz., (i) protectives and
adsorbents (talc, calamine ), (ii)
antimicrobial agents (potassium
permanganate, tincture iodine, boric acid )
and astringents (alum).
1.1 Spectroscopy (15L)
1.1.1 Introduction : Electromagnetic
spectrum, units of wavelength and
USCH603 I frequency.
2.5 1 1.1.2 UV - Visible Spectroscopy: Basic
theory, solvents, nature of UV -VIS
spectrum, concept of Chromophore,
auxochrome,bathochromic
shift,Hypsochromic shift hyperchromic
Page 28
effect and chromophore -auxochrome
interactions.
1.1.3 IR Spectrocopy: Basic theory, nature
of IR spectrum, selection rule , fingerprint
region.
1.1.4 PMR Spectroscopy: Basic theory of
NMR, nature of PMR spectrum, chemical
shift (∂ unit), standard for PMR, solvents
used. Factors affecting chemical shift:
(1) induc tive effect (2) anisotropic effect
(with reference to C=C, CΞC, C=O and
benzene ring). Spin - spin coupling and
coupling constant. Proton exchange -
application of deuterium exchange
,Application of PMR in structure
determination.
1.1.5 Spectral characteristics of following
classes of organic compounds, including
benzene and monosubstituted benzenes,
with respect to UV -VIS, IR,PMR:
(1)alkanes (2)alkenes and polyenes (3)
alkynes (4) haloalkanes (5) alcohols
(6) carbonyl compounds (7) ethers (8)
carboxylic acids (9) e sters (10)amines
(11) amides (broad regions characteristic of
different groups are expected).
1.1.6 Mass Spectrometry: Basic
theory.Nature of mass spectrum. General
rules of fragmentation. Importance of -
molecular ion peak, isotopic peaks,
basepeak, Nitrogen ru le.Illustrative
fragmentation of alkanes and aliphatic
carbonyl compounds (No Mclafferty
rearrangement).
1.1.7 Problems of structure elucidation of
simple organic compounds using individual
or combined use of the above spectroscopic
technique are expected.(index of
hydrogen deficiency should be the first step
in solving the problems).
2.1 Polymers (11L)
2.1.1 Introduction: General idea of
monomers, polymers, and polymerization,
natural and synthetic polymers.
II Homoplymers and copolymers. 1 Class ification of polymers - Plastic, fibres,
resins, elastomers. Thermoplastics and
thermosets. Copolymers -alternating, block,
random, graft.
2.1.2 Mechanism of free radical addition
Page 29
polymerization.
2.1.3 Elastomers: Natural and synthetic
rubbers. Diene polymerization: 1,2 - and
1,4- addition (cis and trans) polymerization
of isoprene. 1,3 -Butadiene -styrene
copolymer.
2.1.4 Stereochemistry of polymers:
Tacticity. Role of Ziegler -Natta catalyst
(co- ordination polymerization) in directin g
the tacticity in polypropylene (no
mechanism).
2.1.5 Preparation & use of polymers:
(1) Addition polymers: (a) polyethylene
(b)polypropylene (c) PVC (d) polystyrene
(e) polyacrylonitrile (f) polyvinylalcohol
(g) Teflon.
(2) Condensation Polymers: (a) Polyesters
(b) polya mides (c) polyurethans (d)phenol -
formaldehyde resin (e) epoxy resin (f)
polycarbonates.
2.1.6 Recyclable polymers. Biodegradable
polymers and their uses. Biomedical use of
polymers.
2.1.7 Additives to polymers: Plasticizers
,stabilizers and fillers.(The st udents are
expected to identify monomers in a given
polymer and draw the structure of a polymer
from a given set of monomers).
2.2 Photochemistry
2.2.1 Introduction: Difference between
thermal and photochemical reactions.
Jablonski diagram, singlet and t riple states,
allowed and forbidden transitions, fate of
excited molecules, photosensitization. 2.2.2
Photochemical reactions of olefins:
photoisomerisation, photochemical
rearrangement of 1,4 -dienes (di π methane)
2.2.3 Photochemistry of carbonyl
compounds: Norrish I, Norrish II cleavages,
Photo reduction (e.g. benzophenone to
benzpinacol).
3.1 Cat alysts and Reagents (5L)
Study of the following catalysts and
reagents with respect to functional group
transformations and selectivity (no
mechanism). III 3.1.1 Catalysts : Catalysts for 1 hydrogenation:
Raney Ni,Pt and PtO 2: C=C, CN, N O2,
aromatic ring; Pd/C: C=C, COCl →CHO
(Rosenmund); Lindlar catalyst: alkynes;
Wilkinson’s catalyst for
Page 30
stereo selective reduction of olefins.
3.1.2 Reagents : (1)LiAlH 4 and Red -Al:
reduction of CO,COOR, CN, NO 2. (2)
NaBH 4: reduction of CO (3) SeO 2:
hydroxylation of allylic and benzylic
positions,oxidation of CH 2, alpha to CO to
CO.(5)mCPBA and R -OOH/H 2O2 for
epoxidation of C=C. (6) NBS: allylic and
benzylic bromination of position alpha to
CO.
3.2 Natural Products (10L)
3.2.1 Introduction: Primary and secondary
metabolites. Introduction to the following
natural products with respect to the sources
and classes. (Structures of the
compounds specified below are expected).
(a) Terpene: Isop rene and special isoprene
rule.α -terpeniol, citral,camphor, α -pinene.
(b) Alkaloids: nicotine,atropine.
(c) Vitamins: Vitamins A and C.
(d) Hormones: adrenaline, thyroxine.
(e) Steroids: cholesterol, progesterone.
3.2.2 Struct ure determination of natural
products: 3.2.2.1 Ozonolysis in terpenoids -
Examples of open chain and monocyclic
monoterpenes. 3.2.2.2 Hofmann exhaustive
methylation and degradation in alkaloids –
simple open chain and monocyclic
amines.3.2.2.3 Structure determination of
citral and nicotine through degradation
studies. Total synthesis of degradation
studies. Total synthesis of (i) Citral from
3-methylbutan -1-ol (ii) Nicotine from
nicotinic acid.
3.2.4 Commercial importance of
terpenoids and alkaloids:
Synthesis of camphor from α -
pinene, α and β ionones,
geraniol and nerol from citral.
3.2.5
4.1 Organometallic Chemistry (5L)
4.1.1 Intoduction: Carbon -metal bon d-
Nature, types reactivity.
4.1.2 Organo magnesium Compounds :
IV Grignard reagent :Preparation, structure,
1 and stability, Reaction with compounds
containing acidic hydrogen,carbonyl
compounds, cyanides and CO 2.
4.1.3 Organolithium Compounds :
Preparation using alkyl/aryl halides.
Reactions with compounds containing
Page 31
acidic hydrogen, alkyl halides, carbonyl
compounds, cyanides and CO 2. Lithium
dialkyl cuprates: Preparation and reactions
with aliphatic /aromatic/vinylic halides.
4.1.4 Organozinc compounds : Preparation
of dialkyl zinc. Reaction with water, acid
chlorides and alkyl halides. Reformatsky
reaction (with mechanism).
4.2 Chemistry of some Important
Biomolecules: (10L)
4.2.1 α -Amino acids:
Structure,configuration,Essential amino
acids and their abbreviations, classification,
Properties: pH dependency of ionic
structure and isoelectric point. Methods of
preparations: Strecker synthesis,
amid omalonate synthesis, Erlenmeyer
azalactone synthesis.
4.2.2 Polypeptides and Proteins:
Polypeptides: Peptide bond. Nomenclature
and representation of polypeptides.
Merrifields solid phase peptide synthesis
(example of di - and tri- peptides for
nomenclature and synthesis). Proteins:
Sources, types,functions,colloidal nature,
separation based on isoelectric point,
denaturation and functions. Partial and total
hydrolysis. General idea of primary,
secondary, tertiary and quartenary
structures.
4.2.3 Nucleic acids: Selective hydrolysis of
nucleic acids.Sugars and bases in nucleic
acids. Stuctures of nucleosides an
nucleotides in DNA and RNA. Structure of
nucleic acids (DNA and RNA): Base
pairing in nucleic acids. Importance of
nucleic acids -self duplication, protein
synthesis.
Electroanalytical methods. (15L)
1.1 D.C. Polaroghraphy (11L): Polarizable
and nonpolarizable electrodes, basic
principles, residual current, diffusion
USCH604 I current, limiting current, dropping mercury
2.5 1 electrode, supporting electrolyte half wave
potential, derivation of the polarographic
wave equation for a reversible reaction.
Ilkovic equation, oxygen interference and
its removal, maxima and maxima
suppressors, polarographic cell, qualitative
Page 32
and quantitativeanalysis, calibration curve
and standard addition method, applications.
[Numerical problems exp ected]
1.2 Amperometric Titrations: Basic
principles, rotating platinum electrode and
nature of the titration curves, applications,
advantages and limitations.
Methods of separation -II (15L)
2.1 Gas chromatography (6L): Gas liquid
chromatography, basic principles retention
time, retention volume, resolution, peak
width theoretical plates. HETP,
instrumentation, columns, detectors,
applications.
II 2.2 High Performance Liquid
1 Chromatograp hy (4L): Instrumentation,
types of elution, U.V. and I.R. detector and
applications
2.3 Ion Exchange Chromatography (5L):
Types of ion exchangers, mechanism of ion
exchange, selectivity coefficients and
separation factors, cap acity and its
determination, factors affecting the
separation of ions, applications.
Treatment of analytical data -II and
Titrimetric analysis -II (15L)
3.1 Treatment of Analytical Data (6L):
Distribution of random errors, Gaussian
curve, students’ t, confidence limits and
confidence interval, criteria for rejection of
result: 2.5d rule,4.0 rule and Q test, F teset,
testing for significance, null hypothesis,
method of averages, least squares method.
Numerical problems expected]
3.2 Complexometric Titrations (5L):
III General introduction, EDTA titrations,
1 advantages and limitations of EDTA as the
titrant, absolute and conditional formation
constants of metal EDTA complex es,
construction of titration curves, types of
EDTA titrations,methods of increasing the
selectivity of EDTA as a titrant,
metallochromic indicators, theory and
applications.
3.3 Redox Titrations (4L): General
introductio n, theory of redox indicators,
criterion for choosing an indicator for a
redox titration, construction of the titration
curves in the case of (1) Fe (II) Vs. Ce(IV )
Page 33
(2) Fe (II) Vs. dichromate, use of diphenyl
amine and f erroin as redox indicators.
Concepts in Quality and miscellaneous
methods (15L)
4.1 Total quality management (5L) :
concept of quality, quality control, quality
assurance total quality management, ISO
series, Good labora tory practices
4.2 Mass Spectrometry (2L): Basic
IV principles, introduction of components only 1 4.3 Thermal Methods (5L): Classification
of thermal methods, thermogravimetric
analysis,basic principles, instrumentation
factors affecting the TG curve, applications
4.4 Introduction to Radio Analytical
Techniques (3L): Classification of the
techniques, introduction to neutron
activation analysis and its applications.
Practicals
Practicals of Course USCH601
Physical Practicals
Chemical Kinetics –
To determine the energy of activation for the
acid catalysed hydrolysis of methyl acetate.
Partition coefficient
To determine the equilibrium constant for the
reactionKI + I 2 KI3 by partition method.
(Partion coefficient of I 2 between CCl 4 and
water is to be given)
USCHP07 Potentiometry – 3 8
1. To determine the strength of the given
strong acid (HCl) by potentiometric
titration using quinhydrone electrode
(Calculation of pH fr om E cell and the
plot of (a)
against V
(b) pH against V graphs are expected).
OR
To determine pKa value of the given
weak monobasic acid (CH 3COOH)
by e.m.f. measurements.
2. To determine E cal at room temperature
Page 34
and using this value, determ ine
standard reduction potential of
Ag/Ag+ electrode at room
temperature.
Conductometry –
To determine the amount of dibasic acid
(Oxalic acid) by conductometric titration
against strong base.
OR
To determine the relative strength of
monochloroaceti c acid and acetic acid
conductometrically.
Course USCH602
Inorganic Practicals
Inorganic preparations
1. Mercury tetrathiocyanato Cobaltate (II)
Hg[Co(SCN) 4]
2. Magnesium oxinate[Mg(Ox) 2]
3. Tris-acetyl acetonato iron(III)
[Fe(AcAc) 3]
4. Tetrammine copper(II) sulp hate.
[Cu(NH 3)4]SO 4.H2O
Inorganic estimations/ Analysis
1. Estimation of copper iodometrically
using sodium thiosulphate. ( Students are
expected to standardize supplied sodium
thiosulphate solution using potassium
dichromate)
2. Estimation of lead by compl exomety
using EDTA solution. ( Students are expected
to standardize the supplied EDTA solution.
Suggested standard for standardization:
ZnSO 4.7H 2O)
Practicals of Course USCH603
Organic Practicals
Binary Mixture Separation
USCHP08 Seperation of mixture containing (VL + NVL)
3 8 & (S + VL) components.
Organic Preparations
1. Aniline/p‐toluidine → N‐Acetyl derivative
2. Salicylic acid/nitrobenzene/ Acetanilide
→ Nitro derivative
Page 35
3. β‐ naphthol → Methyl Eth er derivative
(Using dimethyl sulphate)
4. Acetanilide →
p‐bromoacetanilide derivative
5. Aniline/ p‐toluidine → Schiff base
with benzaldehyde
6. Hydroquinone/beta naphthol →
Acetyl derivative
7. Methyl salicylate/ethyl benzoate → Acid
derivative (Hydrolysis)
8. Benzaldehyde/p‐nitrobenzaldehyde →
Acid (Oxidation)
Course USCH604
Analytical Practicals
1. Determination of chemical oxygen
demand of a water sample.
2. Determination of percentage purity of
a sample of common salt using a
cation exchanger.
3. Determination of po tassium content of
a commercial salt sample by flame
photometry.
4. Determination of acetic acid content
of a vinegar sample by potentiometric
titration with sodium hydroxide using
quinhydrone.
5. Determination of Cr (VI) in the given
solution as dichromate by the method
of least squares,
spectrophotometrically
Page 36
Reference List for Paper -I (Physical Chemistry)
1. Physical Chemistry, Ira Levine, 5th Edition, 2002 Tata McGraw Hill
Publishing Co.Ltd.
2. Physical Chemistry, P.C. Rakshit, 6th Edition, 2001, Sarat Book
Distributors, Kolkota.
3. Physical Chemistry, R.J. Silbey, & R.A. Alberty, 3rd edition , John
Wiley & Sons, Inc [part 1]
4. Physical Chemistry, G. Castellan, 3rd edition, 5th Reprint, 1995
Narosa Publishing House.
5. Modern Electrochemistry, J.O.M Bockri s & A.K.N. Reddy, Maria
Gamboa – Aldeco 2nd Edition, 1st Indian reprint,2006 Springer
6. Visible & U.V. Spectroscopy, Analytical Chemsitry by Open Learning
R. Demny and R. Sinclair M 1991 John Wiley & Sons
7. Classical Methods , Vol 1 Analytical Chemistry by O pen Learning D.
Cooper & C. Devan,1991 John Wiley & Sons
8. Physical Chemistry, G.M. Barrow, 6th Edition, Tata McGraw Hill
Publishing Co. Ltd. New Delhi.
9. The Elements of Physical Chemistry, P.W. Atkins, 2nd Edition, Oxford
Universtity Press Oxford
10. Physical C hemistry, G.K. Vemullapallie, 1997, Prentice Hall of India,
Pvt.Ltd. New Delhi.
References for Paper -II.(Inorganic Chemistry).
1. D. Banerjea, Coordination chemistry, Tata McGraw Hill, New Delhi,
(1993).
2. D. F. Shriver and P. W. Atkins, Inorganic chemistry, 3rd Ed., Oxford
University Press, (1999).
3. K. F. Purcell and J. C. Kotz, Inorganic chemistry, Saunders, Hongkong,
(1977).
4. N. N. Greenwood and E. Earnshaw, Chemistry of elements, Pergamon
Press, Singapore, (1989).
5. W. L. Jolly, Modern inor ganic chemistry, 2nd Ed. McGraw Hill Book
Co., (1991).
6. B. E. Douglas and H. McDaniel, Concepts and models in inorganic
chemistry, 3rd Ed., John Wiley & Sons, Inc., New York, (1994).
7. G. N. Mukherjee and A. Das, Elements of bioinorganic chemistry, Dhuri
and Sons, Calcutta, (1988).
8. R. W. Hay, Bioinorganic chemistry, Ellis Harwood, England, (1984).
Page 37
9. R. C. Mehrotra and A. Singh, Organometallic chemistry: A unified
approach, Wiley Eastern, New Delhi, (1991).
10. For synthesis of iron ethylenediamine sulphate refer Pr actical Inorganic
Chemistry by G. Marr and B. W. Rockett,Van Nostrand Reinhold
Company London1972. P 34.
11. For preparation of CuCl 2.2DMSO Refer Microscale Inorganic Chemistry
by Z. Szafran, Ronald M. Pike and Mono M. Singh. Pub. John Wiley and
Sons1991.p.218 .
References For Paper -III (Organic Chemistry)
1. Organic Chemistry, Francis A Carey, Pearson Education, 6th Edition,
Special Indian Edition 2008
2. Organic Chemistry, R.T. Morrison and R.N. Boyd, 6th Edition, Pearson
Edition
3. Organic Chemistry, T.W.G. Solomon a nd C.B. Fryhle, 8th Edition, John
Wiley & Sons, 2004
4. A guide to mechanism in Organic Chemistry, 6th Edition, Peter Sykes,
Pearson Education
5. Fundamentals of Organic Chemistry , G. Marc Loudon, 4th Edition
Oxford
6. Organic Chemistry, L.G. Wade Jr and M.S. Sing h, 6th Edition,2008
7. Organic Chemistry Baula Y. Bruice, Pearson Edition, 2008
8. Organic Chemistry,J.G. Smith, 2nd Editionm Special Indian Edition, Tata
McGraw Hill
9. Organic Chemistry, S.H. Pine, McGraw Hill Kogakusha Ltd.
10. Stereochemistry, P.S. Kalsi, New Age International Ltd. 4th Edition,2006
Reference List for Paper -IV (Analytical Chemistry)
1. D. Harvey, Modern Analytical Chemistry, The McGraw -Hill Pub. 1st
Edition (2000)
2. H.S. Ray, R Sridhar and K.P. Abraham, Extraction of Nonferrous Metals,
Affilia tedEast -West Press Pvt. Ltd. New Delhi (1985) reprint 2007.
3. G.H. Jeffery, J. Bassett, J. Mendham and R.C. Denney , Vogel’s Textbook
of Qunatitative Chemical Analysis, Fifth edition, ELBS Publication (1996)
4. D.A. Skoog D.M. West and F.J. Holler, Fundametals of Analytical
Chemistry, 7thEdition (printed in India in 2001) ISBN Publication.
5. Analytical Chemistry, J.G. Dick,1973 Tata McGraw Hill Publishing Co. Ltd.
New Delhi.
6. Quantitative analysis, Dey & Underwood, Prentice Hall of India, Pvt. Ltd.
Page 38
New Delhi
7. Funda mentals of Analytical Chemistry, Skoog etal 8th edition, Saunders
college publishing.