GATE 2014 Syllabus for Chemistry (CY)
PHYSICAL
CHEMISTRY
Structure: Quantum theory: principles and techniques;
applications to a particle in a box, harmonic oscillator, rigid rotor and
hydrogen atom; valence bond and molecular orbital theories, Hückel
approximation; approximate techniques: variation and perturbation; symmetry,
point groups; rotational, vibrational, electronic, NMR, and ESR spectroscopy
Equilibrium: Kinetic theory of gases; First law of
thermodynamics, heat, energy, and work; second law of thermodynamics and
entropy; third law and absolute entropy; free energy; partial molar quantities;
ideal and non-ideal solutions; phase transformation: phase rule and phase
diagrams – one, two, and three component systems; activity, activity
coefficient, fugacity, and fugacity coefficient; chemical equilibrium, response
of chemical equilibrium to temperature and pressure; colligative properties;
Debye-Hückel theory; thermodynamics of electrochemical cells; standard
electrode potentials: applications – corrosion and energy conversion; molecular
partition function (translational, rotational, vibrational, and electronic).
Kinetics: Rates of chemical reactions, temperature
dependence of chemical reactions; elementary, consecutive, and parallel
reactions; steady state approximation; theories of reaction rates – collision
and transition state theory, relaxation kinetics, kinetics of photochemical
reactions and free radical polymerization, homogeneous catalysis, adsorption
isotherms and heterogeneous catalysis.
INORGANIC
CHEMISTRY
Main
group elements: General
characteristics, allotropes, structure and reactions of simple and industrially
important compounds: boranes, carboranes, silicones, silicates, boron nitride,
borazines and phosphazenes. Hydrides, oxides and oxoacids of pnictogens (N, P),
chalcogens (S, Se & Te) and halogens, xenon compounds, pseudo halogens and
interhalogen compounds.Shapes of molecules and hard- soft acid base concept.
Structure and Bonding (VBT) of B, Al, Si, N, P, S, Cl compounds. Allotropes of
carbon: graphite, diamond, C60. Synthesis and
reactivity of inorganic polymers of Si and P.
Transition
Elements: General
characteristics of d and f block elements; coordination chemistry: structure
and isomerism, stability, theories of metal- ligand bonding (CFT and LFT),
mechanisms of substitution and electron transfer reactions of coordination
complexes. Electronic spectra and magnetic properties of transition metal
complexes, lanthanides and actinides. Metal carbonyls, metal- metal bonds and
metal atom clusters, metallocenes; transition metal complexes with bonds to hydrogen,
alkyls, alkenes and arenes; metal carbenes; use of organometallic compounds as
catalysts in organic synthesis. Bioinorganic chemistry of Na, K. Mg, Ca, Fe,
Co, Zn, Cu andMo.
Solids: Crystal systems and lattices, miller
planes, crystal packing, crystal defects; Bragg’s Law, ionic crystals, band
theory, metals and semiconductors, Different structures of AX, AX2, ABX3 compounds,
spinels.
Instrumental
methods of analysis: Atomic absorption
and emission spectroscopy including ICP-AES, UV- visible spectrophotometry,
NMR, mass, Mossbauer spectroscopy (Fe and Sn), ESR spectroscopy, chromatography
including GC and HPLC and electro-analytical methods (Coulometry, cyclic
voltammetry, polarography – amperometry, and ion selective electrodes).
ORGANIC
CHEMISTRY
Stereochemistry: Chirality of organic molecules with or
without chiral centres. Specification of configuration in compounds having one
or more stereogeniccentres. Enantiotopic and diastereotopic atoms, groups and
faces. Stereoselective and stereospecific synthesis. Conformational analysis of
acyclic and cyclic compounds. Geometrical isomerism. Configurational and
conformational effects on reactivity and selectivity/specificity.
Reaction
mechanism: Methods of
determining reaction mechanisms. Nucleophilic and electrophilic substitutions
and additions to multiple bonds. Elimination reactions. Reactive intermediates-
carbocations, carbanions, carbenes, nitrenes, arynes, free radicals. Molecular
rearrangements involving electron deficient atoms.
Organic
synthesis: Synthesis,
reactions, mechanisms and selectivity involving the following- alkenes,
alkynes, arenes, alcohols, phenols, aldehydes, ketones, carboxylic acids and
their derivatives, halides, nitro compounds and amines. Use of compounds of Mg,
Li, Cu, B and Si in organic synthesis. Concepts in multistep synthesis-
retrosynthetic analysis, disconnections, synthons, synthetic equivalents,
reactivity umpolung, selectivity, protection and deprotection of functional
groups.
Pericyclic
reactions: Electrocyclic, cycloaddition
and sigmatropic reactions. Orbital correlation, FMO and PMO treatments.
Photochemistry: Basic principles. Photochemistry of alkenes,
carbonyl compounds, and arenes. Photooxidation and photoreduction. Di-Ï€-
methane rearrangement, Barton reaction.
Heterocyclic
compounds: Structure,
preparation, properties and reactions of furan, pyrrole, thiophene, pyridine,
indole and their derivatives.
Biomolecules: Structure, properties and reactions of mono-
and di-saccharides, physicochemical properties of amino acids, chemical
synthesis of peptides, structural features of proteins, nucleic acids,
steroids, terpenoids, carotenoids, and alkaloids.
Spectroscopy: Principles and applications of UV-visible,
IR, NMR and Mass spectrometry in the determination of structures of organic
molecules.
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