JEE Advanced 2024 Chemistry Syllabus: This article hands out the complete and revised JEE Advanced Chemistry Syllabus 2024 for JEE Advanced 2024 aspirants. We have also provided you a PDF link to download and save the complete chemistry syllabus for future reference. The JEE Advanced Chemistry 2024 syllabus is the same as the previous year. No changes have been made in the syllabus for 2024 aspirants, thus giving them a dominance over understanding the exam pattern and competency level of questions.
Joint Entrance Examination (JEE), one of the toughest exams in India is held by the seven zonal coordinating IITs under the guidance of the Joint Admission Board(JAB). This exam is conducted for students willing to get admission into the Indian Institutes of Technology (IIT). Any student willing to join IIT will first have to appear for the JEE Mains exam followed by the JEE Advanced. After cracking both of these examinations, students have to then sit through interviews, in order to be a student of IIT.
Students have to go through rigorous preparation and training sessions to clear JEE Mains & JEE Advanced exams. Hectic and exhaustive study schedules, tight preparation, mock tests, coaching, and a lot more goes into cracking IIT. Generally, students start their preparation two years prior to their appearing academic year and most of them start in their higher secondary. But, the first and the most crucial step in the preparation for clearing any exam happens to be, checking the syllabus of the examination.
JEE Advanced 2024 Chemistry Syllabus
Check the detailed, revised chapter-wise JEE Advanced Chemistry Syllabus 2024 from the table below.
| 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 ȟܩ and ȟܩٓ 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 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. respective groups.
|
| 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 (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 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 co-polymers; 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. |
To download JEE Advanced Chemistry Syllabus 2024, click on the link below
| Download JEE Advanced Chemistry Syllabus 2024 |
As you can see, the JEE Advanced 2024 Chemistry syllabus is quite vast and detailed. It’s a long syllabus with loads of topics to cover. Thus, students must start their preparation as soon as possible. Though chemistry is a scoring subject, it can weaken your score if not practiced consistently. Chemistry is famous for its exceptions and these exceptions make a lot of questions in the question paper. Thus, each of the exceptions must be carefully read and practiced. It can be confusing and troublesome, but if you clear your concepts and practice regularly, Chemistry can be a win-win in the JEE Advanced Examination 2024.
Important Links:
|
|
-1752826559487.jpg)
Comments
All Comments (0)
Join the conversation