JEE ADVANCED 2014 Syllabus

JEE Advanced 2014

JEE Advanced 2014 Chemistry Syllabus Physical chemistry

General topics: conception of atoms and molecules; Dalton’s atomic theory; Mole concept; Chemical formulae; Balanced chemical equations; Calculations (based on mole concept) involving common oxidoreduction, neutralisation, and displacement reactions; Concentration in terms of mole fraction, molarity, concentration and normality.

Gaseous and liquid states: temperature scale of temperature, gas equation; Deviation from quality, van der Waals equation; kinetic theory of gases of gases, average, root mean sq. and most probable velocities and their relation with temperature; Law of partial pressures; Vapour pressure; Diffusion of gases.

Atomic structure and chemical bonding: Bohr model, spectrum of atom, quantum numbers; property, Broglie hypothesis; Uncertainty principle; Qualitative quantum mechanical image of atom, shapes of s, p and d orbitals; Electronic configurations of parts (up to number 36); Aufbau principle; Pauli’s law of nature and Hund’s rule; Orbital overlap and valence bond; sexual union involving s, p and d orbitals only; Orbital energy diagrams for homonuclear matter species; chemical element bond; Polarity in molecules, moment (qualitative aspects only); VSEPR model and shapes of molecules (linear, angular, triangular, sq. tabular, pyramidal, sq. pointed, symmetrical  bipyramidal, tetrahedral and octahedral).

Energetics: initial law of thermodynamics; Internal energy, work and warmth, pressure-volume work; heat content, Hess’s law; Heat of reaction, fusion and vapourization; Second law of thermodynamics; Entropy; Free energy; Criterion of naturalness.

Chemical equilibrium: Law of mass action; constant, lupus erythematosus Chatelier’s principle (effect of concentration, temperature and pressure); Significance of ΔG and ΔG° in chemical equilibrium; Solubility product, common particle impact, hydrogen ion concentration and buffer solutions;  Acids and bases (Bronsted and Lewis concepts); reaction of salts.

Electrochemistry: chemical science cells and cell reactions; normal conductor potentials; chemist equation and its relevancy ΔG; electromotive force series, electrical phenomenon of galvanic cells; Faraday’s laws of electrolysis; Electrolytic electrical phenomenon, specific, equivalent and molar conduction, Kohlrausch’s law; Concentration cells.

Chemical kinetics: Rates of chemical reactions; Order of reactions; Rate constant; initial order reactions; Temperature dependence of rate constant (Arrhenius equation).

Solid state: Classification of solids, crystalline state, seven crystal systems (cell parameters a, b, c, α, β, γ), shut packed structure of solids (cubic), packing in independent agency, bcc and hcp lattices; Nearest neighbours, ionic radii, straightforward ionic compounds, purpose defects.

Solutions: Raoult’s law; mass determination from lowering of pressure level, elevation of boiling purpose and depression of temperature.

Surface chemistry: Elementary ideas of surface assimilation (excluding surface assimilation isotherms); Colloids: varieties, strategies of preparation and general properties; Elementary concepts of emulsions, surfactants and micelles (only definitions and examples).

Nuclear chemistry: Radioactivity: isotopes and isobars; Properties of α, β and γ rays; mechanics of disintegration (decay series excluded), carbon dating; Stability of nuclei with reference to proton-neutron ratio; transient discussion on fission and fusion reactions.

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Inorganic Chemistry

Isolation/preparation and properties of the subsequent non-metals: element, silicon, nitrogen, phosphorus, oxygen, sulphur and halogens; Properties of allotropes of carbon (only diamond and graphite), phosphorus and sulphur.

Preparation and properties of the subsequent compounds: Oxides, peroxides, hydroxides, carbonates, bicarbonates, chlorides and sulphates of metallic element, potassium, metallic element and calcium; Boron: diborane, chemical element acid and borax; Aluminium: corundom, chloride and alums; Carbon: oxides and acid (carbonic acid); Silicon: silicones, silicates and semiconductor carbide;  Nitrogen: oxides, oxyacids and ammonia; Phosphorus: oxides, oxyacids (phosphorus acid, phosphorous acid) and phosphine; Oxygen: gas and chemical element peroxide; Sulphur: chemical element compound, oxides, sulphurous acid, vitriol and metallic element thiosulphate; Halogens: hydrohalic acids, oxides and oxyacids of halogen, bleaching powder; chemical element fluorides.

Transition parts (3d series): Definition, general characteristics, reaction states and their stabilities, color (excluding the small print of electronic transitions) and calculation of spin-only magnetic moment; Coordination compounds: terminology of mononucleate coordination compounds, cis-trans and ionisation isomerisms, crossbreeding and geometries of mononucleate coordination compounds (linear, tetrahedral, sq. tabular and octahedral).

Preparation and properties of the subsequent compounds: Oxides and chlorides of tin and lead; Oxides, chlorides and sulphates of Fe2+, Cu2+ and Zn2+; permanganate of potash, salt, silver compound, nitrate, silver thiosulphate.

Ores and minerals: ordinarily occurring ores and minerals of iron, copper, tin, lead, magnesium, aluminium, metallic element and silver.

Extractive metallurgy: Chemical principles and reactions solely (industrial details excluded); Carbon reduction technique (iron and tin); Self reduction technique (copper and lead); Electrolytic reduction technique (magnesium and aluminium); industrial process (silver and gold).

Principles of qualitative analysis: teams I to V (only Ag+, Hg2+, Cu2+, Pb2+, Bi3+, Fe3+, Cr3+, Al3+, Ca2+, Ba2+, Zn2+, Mn2+ and Mg2+); Nitrate, halides (excluding fluoride), sulfate and compound.

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Organic Chemistry

Concepts: sexual union of carbon; letter and pi-bonds; Shapes of easy organic molecules; Structural and geometrical state;  Optical isomerism of compounds containing up to 2 uneven centres, (R,S andE,Z terminology excluded); IUPAC terminology of easy organic compounds (only hydrocarbons, mono-functional and bi-functional compounds); Conformations of alkane and alkane series (Newman projections); Resonance and hyperconjugation; Keto-enol tautomerism; Determination of empirical and molecular formulae of easy compounds (only combustion method); chemical element bonds: definition and their effects on physical properties of alcohols and radical acids; Inductive and resonance effects on acidity and basicity of organic acids and bases; Polarity and inductive effects in radical halides; Reactive intermediates made throughout homolytic and heterolytic bond cleavage;  Formation, structure and stability of carbocations, carbanions and free radicals.

Preparation, properties and reactions of alkanes: Homologous series, physical properties of alkanes (melting points, boiling points and density); Combustion and halogenation of alkanes; Preparation of alkanes by Wurtz reaction and chemical action reactions.

Preparation, properties and reactions of alkenes and alkynes: Physical properties of alkenes and alkynes (boiling points, density and dipole moments); Acidity of alkynes; Acid catalysed association of alkenes and alkynes (excluding the stereochemistry of addition and elimination); Reactions of alkenes with KMnO4 and ozone; Reduction of alkenes and alkynes; Preparation of alkenes and alkynes by elimination reactions; Electrophilic addition reactions of alkenes with X2, HX, HOX (X=halogen) and H2O;  Addition reactions of alkynes; Metal acetylides.

Reactions of benzene: Structure and aromaticity; Electrophilic substitution reactions: halogenation, nitration, sulphonation, Friedel-Crafts alkylation and acylation; impact of  o-, m- and p-directing teams in monosubstituted benzenes.

Phenols: Acidity, electrophilic substitution reactions (halogenation, nitration and sulphonation); Reimer-Tieman reaction, Kolbe reaction.

Characteristic reactions of the subsequent (including those mentioned above): radical halides: arrangement reactions of radical carbocation, Grignard reactions,  nucleophilic substitution reactions;  Alcohols: esterification, dehydration and reaction, reaction with metallic element, phosphorus halides, ZnCl2/concentrated HCl, conversion of alcohols into aldehydes and ketones; Ethers:Preparation by Williamson’s  Synthesis; Aldehydes and Ketones: reaction, reduction, organic compound and hydrazone formation; organic compound condensation, Perkin reaction; Cannizzaro reaction; alkyl halide reaction and nucleophilic addition reactions (Grignard addition); radical acids: formation of esters, acid chlorides and amides, organic compound hydrolysis; Amines: basicity of substituted anilines and acyclic  amines, preparation from nitro compounds, reaction with acid, radical coupling reaction of cation salts of aromatic amines, Sandmeyer and connected reactions of cation salts; carbylamine reaction; Haloarenes: nucleophilic aromatic substitution in haloarenes and substituted haloarenes (excluding Benzyne mechanism and Cine substitution).

Carbohydrates: Classification; mono- and di-saccharides (glucose and sucrose); reaction, reduction, organic compound formation and reaction of plant product.

Amino acids and peptides: General structure (only primary structure for peptides) and physical properties.

Properties and uses of some vital polymers: Natural rubber, cellulose, nylon, teflon and PVC.

Practical organic chemistry: Detection of parts (N, S, halogens); Detection and identification of the subsequent purposeful groups: group (alcoholic and phenolic), carbonyl (aldehyde and ketone), carboxyl, amino and nitro; Chemical strategies of separation of mono-functional organic compounds from binary mixtures.JEE Advanced 2014 Mathematics Syllabus CLICK HERE