JEE Advanced 2024 Chemistry Syllabus; Download PDF
The JEE Advanced Chemistry syllabus for the year 2024 is now available for download in PDF format on this page. Despite concerns among candidates about potential changes due to the reduction in the JEE Main syllabus, it's important to note that there have been no modifications made to the JEE Advanced syllabus from the previous year. IIT Madras is set to conduct the exam on May 26, and candidates must prepare for all topics outlined in the JEE Advanced Chemistry syllabus, regardless of their presence in the JEE Main syllabus.
JEE Advanced syllabus for Chemistry includes topics like General Topics, States of Matter: Gases and Liquids, Atomic Structure, Chemical Bonding and Molecular Structure, Chemical Thermodynamics, Chemical and Ionic Equilibrium, Electrochemistry, Chemical Kinetics, Solid State, Solutions, Surface Chemistry, Classification of Elements and Periodicity in Properties, Hydrogen, s-Block Elements, p-Block Elements, d-Block Elements, f-Block Elements, Coordination Compounds, Isolation of Metals, Principles of Qualitative Analysis, Environmental Chemistry, Basic Principles of Organic Chemistry, Alkanes, Alkenes and Alkynes, Benzene, Phenols, Alkyl Halides, Alcohols, Ethers, Aldehydes and Ketones, Carboxylic Acids, Amines, Haloarenes, Biomolecules, Polymers, Chemistry in Everyday Life, and Practical Organic Chemistry.
JEE Advanced Syllabus 2024 for Chemistry - Download PDF
For a more detailed overview and comprehensive understanding of the JEE Advanced Chemistry syllabus, candidates are encouraged to download the PDF from the provided link on this page. This will assist in formulating an effective and strategic preparation plan for success in the examination.
JEE Advanced Syllabus 2024 for Physics - Download PDF
JEE Advanced 2024 Chemistry Syllabus - Check Topics Here
The topics in JEE Advanced 2024 syllabus for chemistry are as follows:
JEE Advanced Chemistry Topics | Subtopics |
|---|---|
General Topics | Concept of atoms and molecules; Dalton’s atomic theory; Mole concept; Chemical formulae; Balanced chemical equations; Calculations (based on mole concept and stoichiometry) involving common oxidation-reduction, neutralisation, and displacement reactions; Concentration in terms of mole fraction, molarity, molality and normality. |
States of Matter: Gases and Liquids | Gas laws and ideal gas equation, absolute scale of temperature; 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; Diffusion of gases. Intermolecular interactions: types, distance dependence, and their effect on properties; Liquids: vapour pressure, surface tension, viscosity. |
Atomic Structure | Bohr model, spectrum of hydrogen atom; Wave-particle duality, de Broglie hypothesis; Uncertainty principle; Qualitative quantum mechanical picture of hydrogen atom: Energies, quantum numbers, wave function and probability density (plots only), shapes of s, p and d orbitals; Aufbau principle; Pauli’s exclusion principle and Hund’s rule. |
Chemical Bonding and Molecular Structure | Orbital overlap and covalent bond; Hybridisation involving s, p and d orbitals only; Molecular orbital energy diagrams for homonuclear diatomic species (up to Ne2); Hydrogen bond; Polarity in molecules, dipole moment; VSEPR model and shapes of molecules (linear, angular, triangular, square planar, pyramidal, square pyramidal, trigonal bipyramidal, tetrahedral and octahedral). |
Chemical Thermodynamics | Intensive and extensive properties, state functions, First law of thermodynamics; Internal energy, work (pressure-volume only) and heat; Enthalpy, heat capacity, standard state, Hess’s law; Enthalpy of reaction, fusion and vapourization, and lattice enthalpy; Second law of thermodynamics; Entropy; Gibbs energy; Criteria of equilibrium and spontaneity. |
Chemical and Ionic Equilibrium | Law of mass action; Significance of ÈŸÜ© and ÈŸÜ©ٓ in chemical equilibrium; Equilibrium constant (Kp and Kc) and reaction quotient, Le Chatelier’s principle (effect of concentration, temperature and pressure); Solubility product and its applications, 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; Electrochemical work, Nernst equation; Electrochemical series, emf of galvanic cells; Faraday’s laws of electrolysis; Electrolytic conductance, specific, equivalent and molar conductivity, Kohlrausch’s law; Batteries: Primary and Secondary, fuel cells; Corrosion. |
Chemical Kinetics | Rates of chemical reactions; Order and molecularity of reactions; Rate law, rate constant, half-life; Differential and integrated rate expressions for zero and first order reactions; Temperature dependence of rate constant (Arrhenius equation and activation energy); Catalysis: Homogeneous and heterogeneous, activity and selectivity of solid catalysts, enzyme catalysis and its mechanism. |
Solid State | Classification of solids, crystalline state, seven crystal systems (cell parameters a, b, c, α, β, γ), close packed structure of solids (cubic and hexagonal), packing in fcc, bcc and hcp lattices; Nearest neighbours, ionic radii and radius ratio, point defects |
Solutions | Henry’s law; Raoult’s law; Ideal solutions; Colligative properties: lowering of vapour pressure, elevation of boiling point, depression of freezing point, and osmotic pressure; van’t Hoff factor. |
Surface Chemistry | Elementary concepts of adsorption: Physisorption and Chemisorption, Freundlich adsorption isotherm; Colloids: types, methods of preparation and general properties; Elementary ideas of emulsions, surfactants and micelles (only definitions and examples). |
Classification of Elements and Periodicity in Properties | Modern periodic law and the present form of periodic table; electronic configuration of elements; periodic trends in atomic radius, ionic radius, ionization enthalpy, electron gain enthalpy, valence, oxidation states, electronegativity, and chemical reactivity. |
Hydrogen | Position of hydrogen in periodic table, occurrence, isotopes, preparation, properties and uses of hydrogen; hydrides – ionic, covalent and interstitial; physical and chemical properties of water, heavy water; hydrogen peroxide-preparation, reactions, use and structure; hydrogen as a fuel. |
s-Block Elements | Alkali and alkaline earth metals-reactivity towards air, water, dihydrogen, halogens, acids; their reducing nature including solutions in liquid ammonia; uses of these elements; general characteristics of their oxides, hydroxides, halides, salts of oxoacids; anomalous behaviour of lithium and beryllium; preparation, properties, and uses of compounds of sodium (sodium carbonate, sodium chloride, sodium hydroxide, sodium hydrogen carbonate) and calcium (calcium oxide, calcium hydroxide, calcium carbonate, calcium sulphate). |
p-Block Elements | Oxidation state and trends in chemical reactivity of elements of groups 13-17; anomalous properties of boron, carbon, nitrogen, oxygen, and fluorine with respect to other elements in their respective groups. Group 13: Reactivity towards acids, alkalis, and halogens; preparation, properties, and uses of borax, orthoboric acid, diborane, boron trifluoride, aluminium chloride, and alums; uses of boron and aluminium. Group 14: Reactivity towards water and halogen; allotropes of carbon and uses of carbon; preparation, properties, and uses of carbon monoxide, carbon dioxide, silicon dioxide, silicones, silicates, zeolites. Group 15: Reactivity towards hydrogen, oxygen, and halogen; allotropes of phosphorous; preparation, properties, and uses of dinitrogen, ammonia, nitric acid, phosphine, phosphorus trichloride, phosphorus pentachloride; oxides of nitrogen and oxoacids of phosphorus. Group 16: Reactivity towards hydrogen, oxygen, and halogen; simple oxides; allotropes of sulfur; preparation/manufacture, properties, and uses of dioxygen, ozone, sulfur dioxide, sulfuric acid; oxoacids of sulfur. Group 17: Reactivity towards hydrogen, oxygen, and metals; preparation/manufacture, properties, and uses of chlorine, hydrogen chloride and interhalogen compounds; oxoacids of halogens, bleaching powder. Group 18: Chemical properties and uses; compounds of xenon with fluorine and oxygen. |
d-Block Elements | Oxidation states and their stability; standard electrode potentials; interstitial compounds; alloys; catalytic properties; applications; preparation, structure, and reactions of oxoanions of chromium and manganese. |
f-Block Elements | Lanthanoid and actinoid contractions; oxidation states; general characteristics. |
Coordination Compounds | Werner’s theory; Nomenclature, cis-trans and ionization isomerism, hybridization and geometries (linear, tetrahedral, square planar and octahedral) of mononuclear coordination compounds; Bonding [VBT and CFT (octahedral and tetrahedral fields)]; Magnetic properties (spin-only) and colour of 3d-series coordination compounds; Ligands and spectrochemical series; Stability; Importance and applications; Metal carbonyls. |
Isolation of Metals | Metal ores and their concentration; extraction of crude metal from concentrated ores: thermodynamic (iron, copper, zinc) and electrochemical (aluminium) principles of metallurgy; cyanide process (silver and gold); refining. |
Principles of Qualitative Analysis | Groups I to V (only Ag+ , Hg2+, Cu2+, Pb2+, Fe3+, Cr3+, Al3+, Ca2+, Ba2+, Zn2+, Mn2+ and Mg2+); Nitrate, halides (excluding fluoride), carbonate and bicarbonate, sulphate and sulphide. |
Environmental Chemistry | Atmospheric pollution; water pollution; soil pollution; industrial waste; strategies to control environmental pollution; green chemistry. |
Basic Principles of Organic Chemistry | Hybridisation of carbon; σ and π-bonds; Shapes of simple organic molecules; aromaticity; Structural and geometrical isomerism; Stereoisomers and stereochemical relationship (enantiomers, diastereomers, meso) of compounds containing only up to two asymmetric centres 6 (R,S and E,Z configurations excluded); Determination of empirical and molecular formulae of simple compounds by combustion method only; IUPAC nomenclature of organic molecules (hydrocarbons, including simple cyclic hydrocarbons and their mono-functional and bi-functional derivatives only); Hydrogen bonding effects; Inductive, Resonance and Hyperconjugative effects; Acidity and basicity of organic compounds; Reactive intermediates produced during homolytic and heterolytic bond cleavage; Formation, structure and stability of carbocations, carbanions and free radicals. |
Alkanes | Homologous series; Physical properties (melting points, boiling points and density) and effect of branching on them; Conformations of ethane and butane (Newman projections only); Preparation from alkyl halides and aliphatic carboxylic acids; Reactions: combustion, halogenation (including allylic and benzylic halogenation) and oxidation. |
Alkenes and Alkynes | Physical properties (boiling points, density and dipole moments); Preparation by elimination reactions; Acid catalysed hydration (excluding the stereochemistry of addition and elimination); Metal acetylides; Reactions of alkenes with KMnO4 and ozone; Reduction of alkenes and alkynes; Electrophilic addition reactions of alkenes with X2, HX, HOX, (X=halogen); Effect of peroxide on addition reactions; cyclic polymerization reaction of alkynes. |
Benzene | Structure; Electrophilic substitution reactions: halogenation, nitration, sulphonation, FriedelCrafts alkylation and acylation; Effect of directing groups (monosubstituted benzene) in these reactions. |
Phenols | Physical properties; Preparation, Electrophilic substitution reactions of phenol (halogenation, nitration, sulphonation); Reimer-Tiemann reaction, Kolbe reaction; Esterification; Etherification; Aspirin synthesis; Oxidation and reduction reactions of phenol. |
Alkyl Halides | Rearrangement reactions of alkyl carbocation; Grignard reactions; Nucleophilic substitution reactions and their stereochemical aspects. |
Alcohols | Physical properties; Reactions: esterification, dehydration (formation of alkenes and ethers); Reactions with: sodium, phosphorus halides, ZnCl2/concentrated HCl, thionyl chloride; Conversion of alcohols into aldehydes, ketones and carboxylic acids. |
Ethers | Preparation by Williamson’s synthesis; C-O bond cleavage reactions. |
Aldehydes and Ketones | Preparation of: aldehydes and ketones from acid chlorides and nitriles; aldehydes from esters; benzaldehyde from toluene and benzene; Reactions: oxidation, reduction, oxime and hydrazone 7 formation; Aldol condensation, Cannizzaro reaction; Haloform reaction; Nucleophilic addition reaction with RMgX, NaHSO3, HCN, alcohol, amine. |
Carboxylic Acids | Physical properties; Preparation: from nitriles, Grignard reagents, hydrolysis of esters and amides; Preparation of benzoic acid from alkylbenzenes; Reactions: reduction, halogenation, formation of esters, acid chlorides and amides. |
Amines | Preparation from nitro compounds, nitriles and amides; Reactions: Hoffmann bromamide degradation, Gabriel phthalimide synthesis; Reaction with nitrous acid, Azo coupling reaction of diazonium salts of aromatic amines; Sandmeyer and related reactions of diazonium salts; Carbylamine reaction, Hinsberg test, Alkylation and acylation reactions. |
Haloarenes | Reactions: Fittig, Wurtz-Fittig; Nucleophilic aromatic substitution in haloarenes and substituted haloarenes (excluding benzyne mechanism and cine substitution). |
Biomolecules | Carbohydrates: Classification; Mono- and di-saccharides (glucose and sucrose); Oxidation; Reduction; Glycoside formation and hydrolysis of disaccharides (sucrose, maltose, lactose); Anomers. Proteins: Amino acids; Peptide linkage; Structure of peptides (primary and secondary); Types of proteins (fibrous and globular). Nucleic acids: Chemical composition and structure of DNA and RNA. |
Polymers | Types of polymerization (addition, condensation); Homo and copolymers; Natural rubber; Cellulose; Nylon; Teflon; Bakelite; PVC; Bio-degradable polymers; Applications of polymers. |
Chemistry in Everyday Life | Drug-target interaction; Therapeutic action, and examples (excluding structures), of antacids, antihistamines, tranquilizers, analgesics, antimicrobials, and antifertility drugs; Artificial sweeteners (names only); Soaps, detergents, and cleansing action. |
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. |
Books to Prepare for JEE Advanced 2024 Chemistry
Books play a vital role in preparing for JEE Advanced 2024 Chemistry, and here are some recommended ones by experts:
NCERT: Considered the holy bible for Chemistry, NCERT textbooks are essential for building a strong foundation.
Physical Chemistry by O.P. Tandon: Recommended for its comprehensive coverage of physical chemistry topics.
Organic Chemistry by Morrison and Boyd: A popular choice for understanding organic chemistry concepts.
Inorganic Chemistry by J.D. Lee: Known for its in-depth coverage of inorganic chemistry principles.
Organic Chemistry by Paula Yurkanis Bruice: Another excellent resource for mastering organic chemistry.
JEE Advanced Chemistry Syllabus 2024 vs. JEE Main Chemistry Syllabus 2024:
Topics included in JEE Advanced and not in JEE Main Chemistry:
- Perkins reaction
- Qualitative Analysis of Carbonate ions
- Electrochemistry: Equivalent Conductivity
- Nuclear Chemistry: Radioactivity; Properties of alpha, beta, and gamma 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.
Topics included in JEE Main but not in JEE Advanced Chemistry:
Biomolecules: Vitamins – Classification and functions; Nucleic acids – Chemical constitution of DNA and RNA.
Chemistry in Everyday Life: Chemicals in medicines – Analgesics, tranquillizers, antiseptics, disinfectants, antimicrobials, antifertility drugs, antibiotics, antacids, antihistamines – their meaning and common examples. Chemicals in food – Preservatives, artificial sweetening agents – common examples. Cleansing agents – Soaps and detergents, cleansing action.
These books, coupled with a thorough understanding of the syllabus differences, will aid in effective preparation for both JEE Main and JEE Advanced Chemistry.