JEE Advanced Chemistry syllabus

Organic Chemistry:

• Concepts: Hybridisation of carbon; Sigma and pi-bonds; Shapes of simple organic molecules; Structural and geometrical isomerism;  Optical isomerism of compounds containing up to two asymmetric centres, (R,S and E,Z nomenclature excluded); IUPAC nomenclature of simple organic compounds (only hydrocarbons, mono-functional and bi-functional compounds); Conformations of ethane and butane (Newman projections); Resonance and hyperconjugation; Keto-enol tautomerism; Determination of empirical and molecular formulae of simple compounds (only combustion method); Hydrogen bonds: definition and their effects on physical properties of alcohols and carboxylic acids; Inductive and resonance effects on acidity and basicity of organic acids and bases; Polarity and inductive effects in alkyl halides; Reactive intermediates produced during 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 decarboxylation 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 hydration 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; Effect of  o-, m- and p-directing groups in monosubstituted benzenes.
• henols: Acidity, electrophilic substitution reactions (halogenation, nitration and sulphonation); Reimer-Tieman reaction, Kolbe reaction.
• Characteristic reactions of the following (including those mentioned above):  Alkyl halides: rearrangement reactions of alkyl carbocation, Grignard reactions,  nucleophilic substitution reactions;  Alcohols: esterification, dehydration and oxidation, reaction with sodium, phosphorus halides, ZnCl2/concentrated HCl, conversion of alcohols into aldehydes and ketones; Ethers:Preparation by Williamson’s  Synthesis; Aldehydes and Ketones: oxidation, reduction, oxime and hydrazone formation; aldol condensation, Perkin reaction; Cannizzaro reaction; haloform reaction and nucleophilic addition reactions (Grignard addition);  Carboxylic acids: formation of esters, acid chlorides and amides, ester hydrolysis; Amines: basicity of substituted anilines and aliphatic amines, preparation from nitro compounds, reaction with nitrous acid, azo coupling reaction of diazonium salts of aromatic amines, Sandmeyer and related reactions of diazonium 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); Oxidation, reduction, glycoside formation and hydrolysis of sucrose.
• Amino acids and peptides: General structure (only primary structure for peptides) and physical properties.
• Properties and uses of some important polymers: Natural rubber, cellulose, nylon, teflon and PVC.
• Practical organic chemistry: Detection of elements (N, S, halogens); Detection and identification of the following functional groups: hydroxyl (alcoholic and phenolic), carbonyl (aldehyde and ketone), carboxyl, amino and nitro; Chemical methods of separation of mono-functional organic compounds from binary mixtures.

Inorganic Chemistry:

• Isolation/preparation and properties of the following non-metals: Boron, silicon, nitrogen, phosphorus, oxygen, sulphur and halogens; Properties of allotropes of carbon (only diamond and graphite), phosphorus and sulphur.
• Preparation and properties of the following compounds: Oxides, peroxides, hydroxides, carbonates, bicarbonates, chlorides and sulphates of sodium, potassium, magnesium and calcium; Boron: diborane, boric acid and borax; Aluminium: alumina, aluminium chloride and alums; Carbon: oxides and oxyacid (carbonic acid); Silicon: silicones, silicates and silicon carbide;  Nitrogen: oxides, oxyacids and ammonia; Phosphorus: oxides, oxyacids (phosphorus acid, phosphoric acid) and phosphine; Oxygen: ozone and hydrogen peroxide; Sulphur: hydrogen sulphide, oxides, sulphurous acid, sulphuric acid and sodium thiosulphate; Halogens: hydrohalic acids, oxides and oxyacids of chlorine, bleaching powder; Xenon fluorides.
• Transition elements (3d series): Definition, general characteristics, oxidation states and their stabilities, colour (excluding the details of electronic transitions) and calculation of spin-only magnetic moment; Coordination compounds: nomenclature of mononuclear coordination compounds, cis-trans and ionisation isomerisms, hybridization and geometries of mononuclear coordination compounds (linear, tetrahedral, square planar and octahedral).
• Preparation and properties of the following compounds: Oxides and chlorides of tin and lead; Oxides, chlorides and sulphates of Fe2+, Cu2+ and Zn2+; Potassium permanganate, potassium dichromate, silver oxide, silver nitrate, silver thiosulphate.
• Ores and minerals: Commonly occurring ores and minerals of iron, copper, tin, lead, magnesium, aluminium, zinc and silver.
• Extractive metallurgy: Chemical principles and reactions only (industrial details excluded); Carbon reduction method (iron and tin); Self reduction method (copper and lead); Electrolytic reduction method (magnesium and aluminium); Cyanide process (silver and gold).
• Principles of qualitative analysis: Groups I to V (only Ag+, Hg2+, Cu2+, Pb2+, Bi3+, Fe3+, Cr3+,  Al3+, Ca2+, Ba2+, Zn2+, Mn2+ and Mg2+); Nitrate, halides (excluding fluoride), sulphate and sulphide.

Physical chemistry

• General topics: Concept of atoms and molecules; Dalton’s atomic theory; Mole concept; Chemical formulae; Balanced chemical equations; Calculations (based on mole concept) involving common oxidation-reduction, neutralisation, and displacement reactions; Concentration in terms of mole fraction, molarity, molality and normality.
• Gaseous and liquid states: Absolute scale of temperature, ideal gas equation; Deviation from ideality, van der Waals equation; Kinetic theory of gases, average, root mean square 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 hydrogen atom, quantum numbers; Wave-particle duality, de Broglie hypothesis; Uncertainty principle; Qualitative quantum mechanical picture of hydrogen atom, shapes of s, p and d orbitals; Electronic configurations of elements (up to atomic number 36); Aufbau principle; Pauli’s exclusion principle and Hund’s rule; Orbital overlap and covalent bond; Hybridisation involving s, p and d orbitals only; Orbital energy diagrams for homonuclear diatomic species;  Hydrogen bond; Polarity in molecules, dipole moment (qualitative aspects only); VSEPR model and shapes of molecules (linear, angular, triangular, square planar, pyramidal, square pyramidal, trigonal bipyramidal, tetrahedral and octahedral).
• Energetics: First law of thermodynamics; Internal energy, work and heat, pressure-volume work; Enthalpy, Hess’s law; Heat of reaction, fusion and vapourization; Second law of thermodynamics; Entropy; Free energy; Criterion of spontaneity.
• Chemical equilibrium:  Law of mass action; Equilibrium constant, Le Chatelier’s principle (effect of concentration, temperature and pressure); Significance of ΔG and ΔG° in chemical equilibrium; Solubility product, common ion effect, pH and buffer solutions;  Acids and bases (Bronsted and Lewis concepts); Hydrolysis of salts.
• Electrochemistry: Electrochemical cells and cell reactions; Standard electrode potentials; Nernst equation and its relation to ΔG; Electrochemical series, emf of galvanic cells; Faraday’s laws of electrolysis; Electrolytic conductance, specific, equivalent and molar conductivity, Kohlrausch’s law; Concentration cells.
• Chemical kinetics:  Rates of chemical reactions; Order of reactions; Rate constant; First 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), close packed structure of solids (cubic), packing in fcc, bcc and hcp lattices; Nearest neighbours, ionic radii, simple ionic compounds, point defects.
• Solutions:  Raoult’s law; Molecular weight determination from lowering of vapour pressure, elevation of boiling point and depression of freezing point.
• Surface chemistry:  Elementary concepts of adsorption (excluding adsorption isotherms); Colloids: types, methods of preparation and general properties; Elementary ideas of emulsions, surfactants and micelles (only definitions and examples).
• Nuclear chemistry:  Radioactivity: isotopes and isobars; Properties of α, β and γ rays; Kinetics of radioactive decay (decay series excluded), carbon dating; Stability of nuclei with respect to proton-neutron ratio; Brief discussion on fission and fusion reactions.

ORGANIC CHEMISTRY 

 Principles  Related  to  Practical  Chemistry

•  Detection of extra elements (N,S, halogens) in organic compounds; Detection of the following functional groups: hydroxyl (alcoholic and phenolic), carbonyl (aldehyde and ketone), carboxyl and amino groups in organic compounds.
•  Chemistry involved in the preparation of the following: Inorganic compounds: Mohr’s salt, potash alum.
• Organic compounds: Acetanilide, pnitroacetanilide, aniline yellow, iodoform.
• Chemistry involved in the titrimetric excercises – Acids bases and the use of indicators, oxalic-acid vs KMnO4, Mohr’s salt vs KMnO4.
•  Chemical principles involved in the qualitative salt analysis: Cations – Pb2+ , Cu2+, AI3+, Fe3+, Zn2+, Ni2+, Ca2+, Ba2+, Mg2+, NH4+.
• Anions- CO3 2-, S2-, SO4 2-, NO2-, NO3-, CI -, Br, I. (Insoluble salts excluded).

•  Chemical principles involved in the following experiments:

1. Enthalpy of solution of CuSO4

2. Enthalpy of neutralization of strong acid and strong base.

3. Preparation of lyophilic and lyophobic sols.

4. Kinetic study of reaction of iodide ion with hydrogen peroxide at room temperature.

ORGANIC CHEMISTRY 

 Chemistry  in  Everyday  Life

Chemicals in medicines – Analgesics, tranquilizers, antiseptics, disinfectants, antimicrobials, antifertility drugs, antibiotics, antacids, antihistamins – their meaning and common examples.

Chemicals in food – Preservatives, artificial sweetening agents – common examples.

Cleansing agents – Soaps and detergents, cleansing action.

ORGANIC CHEMISTRY 

 Biomolecules

General introduction and importance of biomolecules.

CARBOHYDRATES – Classification: aldoses and ketoses; monosaccharides (glucose and fructose) and constituent monosaccharides of oligosacchorides (sucrose, lactose and maltose).

PROTEINS – Elementary Idea of ı – amino acids, peptide bond, polypeptides;

Proteins: primary, secondary, tertiary and quaternary structure (qualitative idea only), denaturation of proteins, enzymes.

VITAMINS – Classification and functions.

NUCLEIC ACIDS – Chemical constitution of DNA and RNA.

Biological functions of nucleic acids.

ORGANIC CHEMISTRY 

 Polymers

General introduction and classification of polymers, general methods of polymerization-addition and condensation, copolymerization;

Natural and synthetic rubber and vulcanization; some important polymers with emphasis on their monomers and uses – polythene, nylon, polyester and bakelite.

ORGANIC CHEMISTRY 

 Organic  Compounds  Containing  Nitrogen

General methods of preparation, properties, reactions and uses.

Amines: Nomenclature, classification, structure, basic character and identification of primary, secondary and tertiary amines and their basic character.

Diazonium Salts: Importance in synthetic organic chemistry.

ORGANIC CHEMISTRY 

Organic  Compounds  Containing  Oxygen

General methods of preparation, properties, reactions and uses.

ALCOHOLS, PHENOLS AND ETHERS

Alcohols: Identification of primary, secondary and tertiary alcohols; mechanism of dehydration.

Phenols: Acidic nature, electrophilic substitution reactions: halogenation, nitration and sulphonation, Reimer – Tiemann reaction.

Ethers: Structure.

Aldehyde and Ketones: Nature of carbonyl group;Nucleophilic addition to >C=O group, relative reactivities of aldehydes and ketones; Important reactions such as – Nucleophilic addition reactions (addition of HCN, NH3 and its derivatives),

Grignard reagent; oxidation; reduction (Wolff Kishner and Clemmensen); acidity of ı – hydrogen, aldol condensation, Cannizzaro reaction, Haloform reaction; Chemical tests to distinguish between aldehydes and Ketones.

CARBOXYLIC ACIDS

Acidic strength and factors affecting it.

ORGANIC CHEMISTRY

 Organic  Compounds  Containing  Halogens

General methods of preparation, properties and reactions; Nature of C-X bond;

Mechanisms of substitution reactions.

Uses; Environmental effects of chloroform & iodoform.

ORGANIC CHEMISTRY

 Hydrocarbons

Classification, isomerism, IUPAC nomenclature, general methods of preparation, properties and reactions.

Alkanes – Conformations: Sawhorse and Newman projections (of ethane);

Mechanism of halogenation of alkanes.

Alkenes – Geometrical isomerism; Mechanism of electrophilic addition: addition of hydrogen, halogens, water, hydrogen halides (Markownikoff’s and peroxide effect); Ozonolysis and polymerization.

Alkynes – Acidic character; Addition of hydrogen, halogens, water and hydrogen halides; Polymerization.

Aromatic hydrocarbons – Nomenclature, benzene – structure and aromaticity;

Mechanism of electrophilic substitution: halogenation, nitration, Friedel – Craft’s alkylation and acylation, directive influence of functional group in monosubstituted benzene.

ORGANIC CHEMISTRY

 Some  Basic  Principles  of  Organic  Chemistry

Tetravalency of carbon; Shapes of simple molecules – hybridization (s and p);

Classification of organic compounds based on functional groups: – C = C – , – Ch C – and those containing halogens, oxygen, nitrogen and sulphur;

Homologous series; Isomerism – structural and stereoisomerism.

Nomenclature (Trivial and IUPAC)

Covalent bond fission – Homolytic and heterolytic: free radicals, carbocations and carbanions; stability of carbocations and free radicals, electrophiles and nucleophiles.

Electronic displacement in a covalent bond – Inductive effect, electromeric effect, resonance and hyperconjugation.

ORGANIC CHEMISTRY

 Purification and Characterisation of  Organic  Compounds

• Purification – Crystallization, sublimation, distillation, differential extraction and chromatography – principles and their applications.
• Qualitative analysis – Detection of nitrogen, sulphur, phosphorus and halogens.
• Quantitative analysis (basic principles only) – Estimation of carbon, hydrogen, nitrogen, halogens, sulphur, phosphorus.
• Calculations of empirical formulae and molecular formulae; Numerical problems in organic quantitative analysis.

INORGANIC CHEMISTRY 

 Environmental Chemistry

• Environmental pollution – Atmospheric, water and soil.
• Atmospheric pollution – Tropospheric and Stratospheric
• Tropospheric pollutants – Gaseous pollutants: Oxides of carbon, nitrogen and sulphur, hydrocarbons; their sources, harmful effects and prevention; Green house effect and Global warming; Acid rain;
• Particulate pollutants: Smoke, dust, smog, fumes, mist; their sources, harmful effects and prevention.
• Stratospheric pollution- Formation and breakdown of ozone, depletion of ozone layer – its mechanism and effects.
• Water Pollution – Major pollutants such as, pathogens, organic wastes and chemical pollutants; their harmful effects and prevention.
• Soil pollution – Major pollutants such as: Pesticides (insecticides,. herbicides and fungicides), their harmful effects and prevention.
• Strategies to control environmental pollution.

INORGANIC CHEMISTRY 

Co-Ordination Compounds

• Introduction to co-ordination compounds, Werner’s theory; ligands, coordination number, denticity, chelation; IUPAC nomenclature of mononuclear co-ordination compounds, isomerism; Bonding-Valence bond approach and basic ideas of Crystal field theory, colour and magnetic properties; Importance of co-ordination compounds (in qualitative analysis, extraction of metals and in biological systems).

INORGANIC CHEMISTRY

 d – and f – Block Elements

• Transition Elements
• General introduction, electronic configuration, occurrence and characteristics, general trends in properties of the first row transition elements – physical properties, ionization enthalpy, oxidation states, atomic radii, colour, catalytic behaviour, magnetic properties, complex formation, interstitial compounds, alloy formation; Preparation, properties and uses of K2 Cr2 O7 and KMnO4.
• Inner Transition Elements
• Lanthanoids – Electronic configuration, oxidation states and lanthanoid contraction.
• Actinoids – Electronic configuration and oxidation states.

INORGANIC CHEMISTRY 

 P – Block Elements

• Group – 13 to Group 18 Elements

General Introduction: Electronic configuration and general trends in physical and chemical properties of elements across the periods and down the groups; unique behaviour of the first element in each group.

Groupwise study of the p – block elements

• Group – 13

Preparation, properties and uses of boron and aluminium; properties of boric acid, diborane, boron trifluoride, aluminium chloride and alums.

• Group – 14

Allotropes of carbon, tendency for catenation; Structure & properties of silicates, and zeolites.

• Group – 15

Properties and uses of nitrogen and phosphorus; Allotrophic forms of phosphorus; Preparation, properties, structure and uses of ammonia, nitric acid, phosphine and phosphorus halides, (PCl3, PCl5); Structures of oxides and oxoacids of phosphorus.

• Group – 16

Preparation, properties, structures and uses of ozone; Allotropic forms of sulphur; Preparation, properties, structures and uses of sulphuric acid (including its industrial preparation); Structures of oxoacids of sulphur.

• Group – 17

Preparation, properties and uses of hydrochloric acid; Trends in the acidic nature of hydrogen halides; Structures of Interhalogen compounds and oxides and oxoacids of halogens.

• Group –18

Occurrence and uses of noble gases; Structures of fluorides and oxides of xenon.