Excelling in the JEE Advanced 2026 Chemistry section requires a deep understanding of the entire JEE Advanced syllabus 2026. A focused study is important. The JEE Advanced Chemistry syllabus is carefully aligned with the Class 11 and Class 12 NCERT textbooks. This alignment ensures nationwide consistency in preparation standards. Aspiring candidates are advised to download the detailed Chemistry syllabus from the official website.
In this article, we will look into the JEE Advanced Chemistry syllabus 2026. Moreover, we will also look at the unit-wise weightage and topic-wise weightage for the JEE Advanced Chemistry paper.
JEE Advanced Chemistry Syllabus 2026
A detailed analysis of the JEE Advanced Chemistry syllabus for 2026 has been conducted. This analysis is based on trends from the previous year. The Chemistry syllabus for JEE Advanced 2026 is divided into three main sections:
- Physical Chemistry
- Inorganic Chemistry
- Organic Chemistry.
Furthermore, the JEE Advanced Chemistry syllabus aligns with the Class 11 and Class 12 NCERT textbooks. This alignment ensures consistency across the country. Overall, the syllabus features a total of twenty chapters.
Students can now download the JEE Advanced 2025 Chemistry Syllabus: PDF from the JEE Advanced official website.
Below is the JEE Advanced Chemistry syllabus 2026:
| Chapter Name | SubTopics |
| Physical Chemistry | |
| General topics | Concept of atoms and moleculesDalton’s atomic theory Mole concept; Chemical formulaeBalanced chemical equations Calculations (based on mole concept and stoichiometry) involving common oxidation-reduction, neutralisation, and displacement reactionsConcentration 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 the hydrogen atomWave-particle duality, de Broglie hypothesisUncertainty principleQualitative quantum mechanical picture of the hydrogen atom: Energies, quantum numbers, wave function and probability density (plots only), shapes of s, p and d orbitalsAufbau principlePauli’s exclusion principle and Hund’s rule |
| Chemical Bonding and Molecular Structure | Orbital overlap and covalent bond Hybridisation involving s, p and d orbitals onlyMolecular 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 enthalpySecond law of thermodynamics Entropy; Gibbs energy; Criteria of equilibrium and spontaneity |
| Chemical Equilibrium and Ionic Equilibrium | Law of mass action Significance of ∆𝐺 and ∆𝐺 ⊖ 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 (Brønsted and Lewis concepts)Hydrolysis of salts |
| Electrochemistry | Electrochemical cells and cell reactions Standard electrode potentialsElectrochemical work, Nernst equation Electrochemical series, emf of galvanic cellsFaraday’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 reactionsOrder 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, the Freundlich adsorption isotherm; Colloids: types, methods of preparation and general properties; Elementary ideas of emulsions, surfactants and micelles (only definitions and examples). |
| Inorganic Chemistry | |
| Classification of Elements and Periodicity in Properties(Periodic Table) | Modern periodic law and the present form of the 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 the 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, and salts of oxoacids; anomalous behavior 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 phosphorus; 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 (Metallurgy) | 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. |
| Organic 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 (R, S and E, Z configurations excluded);Determination of empirical and molecular formulae of simple compounds by the combustion method only. IUPAC nomenclature of organic molecules (hydrocarbons, including simple cyclic hydrocarbons and their monofunctional and bi-functional derivatives only); Hydrogen bonding effects; Inductive, Resonance and Hyperconjugative effects;Acidity and basicity of organic compounds; Reactive intermediates are 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 the 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 withand ozone;Reduction of alkenes and alkynes; Electrophilic addition reactions of alkenes with X, HX, HOX, (X=halogen); Effect of peroxide on addition reactions; cyclic polymerization reaction of alkynes. |
| Benzene | Structure; Electrophilic substitution reactions: halogenation, nitration, sulphonation, Friedel-Crafts 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 and Ethers | Alcohols:Physical properties. Reactions: esterification, dehydration (formation of alkenes and ethers); Reactions with: sodium, phosphorus halides, ZnCl/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 formation; Aldol condensation, Cannizzaro reaction; Haloform reaction; Nucleophilic addition reaction with RMgX, NaHSO, HCN, alcohol, and 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;Biodegradable 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. |
Unit-Wise Weightage for JEE Advanced Chemistry Paper
Based on last year’s data, here is the unit-wise weightage for JEE Advanced Chemistry Paper:
| Organic Chemistry | |
| Topic | Marks |
| Chemical Bonding | 8 |
| Coordination Compounds | 6 |
| Metallurgy | 4 |
| P-Block | 11 |
| Qualitative Analysis | 7 |
| Total | 36 |
| Inorganic Chemistry | |
| Topic | Marks |
| Amines | 11 |
| Aromatic Compounds | 6 |
| Biomolecules | 4 |
| Carbonyl compounds | 3 |
| General Organic Chemistry | 8 |
| Polymers | 7 |
| Stereoisomerism | 6 |
| Total | 45 |
| Physical Chemistry | |
| Topic | Marks |
| Atomic Structure & Nuclear Chemistry | 3 |
| Chemical Equilibrium | 6 |
| Chemical Kinetics | 8 |
| Electrochemistry | 3 |
| Gaseous State | 3 |
| Mole Concept | 9 |
| Solution & Colligative Properties | 4 |
| Surface Chemistry | 3 |
| Solid State | 4 |
| Total | 43 |
Important Topic-Wise Weightage for JEE Advanced Chemistry Paper
Based on last year’s data, here is the topic-wise weightage for JEE Advanced Chemistry Paper, along with the number of questions, of the important topics for the Chemistry paper.
| Important Topic | Weightage |
| Aldehydes, Ketones and Carboxylic Acids | 14-15% |
| Atomic Structure | 14-15% |
| Chemical Bonding | 4-5% |
| Coordination Compounds | 4-5% |
| Electrochemistry | 4-5% |
| Hydrocarbons | 13-14% |
| Organic Chemistry | 11-12% |
| p-block Elements | 13-14% |
| Solid State | 4-5% |
| Solutions | 6-7% |
| Thermodynamics | 6-7% |
Conclusion
In conclusion, understanding the JEE Advanced Chemistry syllabus for 2026 is important for success. This syllabus covers key topics, including Organic, Inorganic, and Physical. Moreover, it emphasizes the importance of mastering concepts over mere memorization. Additionally, it is aligned with NCERT textbooks, providing a structured foundation for students.
Candidates should focus on the unit and topic weightage. By doing so, they can strategize their study effectively. Finally, utilizing JEE Advanced Chemistry syllabus will help them prepare thoroughly for JEE Advanced 2026.
Students seeking structured guidance can refer to SPM & Lalans Coaching for expert Chemistry preparation support.
Frequently Asked Questions
1. When will JEE Advanced 2026 be conducted?
The exam date for JEE Advanced 2026 is yet to be announced by the officials. Moreover, candidates must keep checking the official site for any further information.
2. Does the JEE Advanced Chemistry syllabus 2026 change every year?
The syllabus for the JEE Advanced exam is almost the same every year. However, minor changes in topics and weightage are updated on the JEE Advanced official website.
For comparison, students can also check the JEE Main Chemistry weightage 2026 to understand how topics differ between both exams.
3. Is the syllabus of Chemistry for JEE Advanced the same as JEE Main?
While JEE Main and JEE Advanced cover similar topics, they are not the same. JEE Advanced focuses more on the practical aspects of Physics and Chemistry. Thus, a solid grasp of practicals from CBSE Class 11 and Class 12 is important for success.
Students seeking structured guidance can refer to SPM & Lalans Coaching for expert Chemistry preparation support.
