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AFMC / NEET-linked AFMC Admission Chemistry (NEET-UG Academic Component) Syllabus

The Chemistry (NEET-UG Academic Component) syllabus for AFMC / NEET-linked AFMC Admission in full: 4 chapters, 19 topics and 46 sub-topics, every one listed below, plus 55 Chemistry (NEET-UG Academic Component) flashcards with answers.

4Chapters
19Topics
46Sub-topics
55Flashcards

Chemistry (NEET-UG Academic Component) syllabus: all 4 chapters

Expand any chapter to see its topics and sub-topics.

  1. Physical Chemistry

    6 topics
    • Some Basic Concepts of Chemistry
      • Mole concept and stoichiometry
      • Empirical and molecular formula
      • Concentration terms and limiting reagent
    • Atomic Structure
      • Bohr model and hydrogen spectrum
      • Quantum numbers and orbitals
      • Aufbau, Pauli, Hund's rules
    • States of Matter and Thermodynamics
      • Gas laws and ideal gas equation
      • First law, enthalpy and Hess's law
      • Entropy, Gibbs free energy and spontaneity
    • Equilibrium
      • Chemical equilibrium and Le Chatelier's principle
      • Ionic equilibrium, pH, buffers
      • Solubility product and common ion effect
    • Electrochemistry and Kinetics
      • Nernst equation and electrochemical cells
      • Conductance and electrolysis
      • Rate laws, order, molecularity and Arrhenius equation
    • Solutions and Surface Chemistry
      • Colligative properties and Raoult's law
      • Adsorption, catalysis and colloids
  2. Inorganic Chemistry

    5 topics
    • Periodic Classification
      • Modern periodic law and trends
      • Ionization enthalpy, electronegativity, atomic radii
    • Chemical Bonding
      • Ionic and covalent bonding
      • VSEPR theory and hybridisation
      • Molecular orbital theory and hydrogen bonding
    • s-Block and p-Block Elements
      • Alkali and alkaline earth metals
      • Groups 13 to 18 and their compounds
    • d- and f-Block Elements
      • Transition elements and variable oxidation states
      • Lanthanoids and actinoids
    • Coordination Compounds
      • Werner's theory and nomenclature
      • Isomerism and crystal field theory
  3. Organic Chemistry

    5 topics
    • Basic Principles and Hydrocarbons
      • IUPAC nomenclature and isomerism
      • Electronic effects: inductive, resonance, hyperconjugation
      • Alkanes, alkenes, alkynes and aromatic hydrocarbons
    • Reaction Mechanisms
      • Nucleophilic substitution (SN1, SN2)
      • Electrophilic addition and aromatic substitution
      • Elimination reactions
    • Oxygen-Containing Functional Groups
      • Alcohols, phenols and ethers
      • Aldehydes, ketones and carboxylic acids
    • Nitrogen-Containing Compounds and Polymers
      • Amines and diazonium salts
      • Polymers and classification
    • Biomolecules
      • Carbohydrates, proteins and amino acids
      • Nucleic acids, vitamins and hormones
  4. Applied and Everyday Chemistry

    3 topics
    • Chemistry in Everyday Life
      • Drugs and their classification
      • Soaps, detergents and food additives
    • Environmental and Green Chemistry
      • Air and water pollution
      • Green chemistry principles
    • Purification and Analysis
      • Methods of purification and chromatography
      • Qualitative and quantitative analysis

AFMC / NEET-linked AFMC Admission Chemistry (NEET-UG Academic Component) flashcards — 55 questions with answers

  1. State the SI unit and definition of one mole, and the value of Avogadro's number.

    A mole is the amount of substance containing as many entities as there are atoms in 12 g of carbon-12. Avogadro's number = 6.022 x 10^23 entities per mole.

  2. What is the difference between molarity and molality, including their units?

    Molarity (M) = moles of solute per litre of solution (mol/L); it varies with temperature. Molality (m) = moles of solute per kilogram of solvent (mol/kg); it is temperature-independent.

  3. State the law of multiple proportions with an example.

    When two elements combine to form more than one compound, the masses of one element that combine with a fixed mass of the other are in a small whole-number ratio. Example: in CO and CO2, the masses of oxygen per fixed mass of carbon are in the ratio 1:2.

  4. What are the four quantum numbers and what does each specify?

    Principal (n): shell/energy and size. Azimuthal/orbital angular momentum (l): subshell/shape. Magnetic (m_l): orbital orientation. Spin (m_s): electron spin (+1/2 or -1/2).

  5. State Hund's rule of maximum multiplicity.

    Electrons fill degenerate orbitals singly with parallel spins before any orbital is doubly occupied, giving maximum total spin (maximum multiplicity).

  6. Give the de Broglie equation relating wavelength to momentum.

    lambda = h / (mv) = h / p, where h is Planck's constant, m is mass, and v is velocity.

  7. State Heisenberg's uncertainty principle as a formula.

    It is impossible to simultaneously determine the exact position and momentum of a particle: delta(x) x delta(p) >= h / (4*pi).

  8. Write the ideal gas equation and name the variables.

    PV = nRT, where P is pressure, V is volume, n is number of moles, R is the universal gas constant (8.314 J/mol/K), and T is absolute temperature in kelvin.

  9. State the first law of thermodynamics as an equation.

    delta(U) = q + w, where delta(U) is change in internal energy, q is heat absorbed by the system, and w is work done on the system.

  10. Define enthalpy and write the relation between delta(H) and delta(U).

    Enthalpy H = U + PV. For a reaction, delta(H) = delta(U) + delta(n_g)RT, where delta(n_g) is the change in moles of gas.

  11. State Hess's law of constant heat summation.

    The total enthalpy change of a reaction is the same whether it occurs in one step or several steps, because enthalpy is a state function.

  12. Write the Gibbs free energy equation and the criterion for spontaneity.

    delta(G) = delta(H) - T*delta(S). A process is spontaneous when delta(G) < 0, at equilibrium when delta(G) = 0, and non-spontaneous when delta(G) > 0.

  13. State Le Chatelier's principle.

    If a system at equilibrium is disturbed by a change in concentration, pressure, or temperature, the equilibrium shifts in the direction that counteracts the disturbance.

  14. Write the relationship between Kp and Kc for a gaseous equilibrium.

    Kp = Kc(RT)^(delta(n_g)), where delta(n_g) = moles of gaseous products minus moles of gaseous reactants.

  15. Define pH and pOH, and state their relationship at 25 degrees C.

    pH = -log[H+] and pOH = -log[OH-]. At 25 degrees C, pH + pOH = 14.

  16. What is the Henderson-Hasselbalch equation for an acidic buffer?

    pH = pKa + log([salt]/[acid]), where pKa is the negative log of the acid dissociation constant.

  17. Define the common ion effect.

    The suppression of the ionization of a weak electrolyte by the addition of a strong electrolyte that shares a common ion, shifting equilibrium per Le Chatelier's principle.

  18. Write the Nernst equation for an electrode at 298 K (in log form).

    E = E0 - (0.0591/n) log Q, where E0 is the standard electrode potential, n is the number of electrons transferred, and Q is the reaction quotient.

  19. State Faraday's first law of electrolysis.

    The mass of a substance deposited or liberated at an electrode is directly proportional to the quantity of electricity passed: m proportional to Q (where Q = It).

  20. Define molar conductivity and state how it changes with dilution.

    Molar conductivity (Lambda_m) is the conductance of all ions from one mole of electrolyte: Lambda_m = kappa x 1000 / C. It increases with dilution for both strong and weak electrolytes.

Show the other 35 Chemistry (NEET-UG Academic Component) flashcards
  1. Give the integrated rate law and half-life expression for a first-order reaction.

    k = (2.303/t) log([A0]/[A]); half-life t(1/2) = 0.693/k, which is independent of initial concentration.

  2. State the Arrhenius equation relating rate constant to temperature.

    k = A*e^(-Ea/RT), where A is the pre-exponential (frequency) factor, Ea is activation energy, R is the gas constant, and T is absolute temperature.

  3. State Raoult's law for a solution of two volatile liquids.

    The partial vapour pressure of each component is proportional to its mole fraction: p_total = p_A0*x_A + p_B0*x_B.

  4. List the four colligative properties of dilute solutions.

    Relative lowering of vapour pressure, elevation of boiling point, depression of freezing point, and osmotic pressure.

  5. Define the van't Hoff factor (i).

    i is the ratio of the observed colligative property to the calculated value assuming no association/dissociation; it equals the actual number of particles in solution per formula unit (i > 1 for dissociation, i < 1 for association).

  6. Differentiate between physisorption and chemisorption.

    Physisorption involves weak van der Waals forces, is reversible, has low enthalpy, and decreases with temperature. Chemisorption involves chemical bonds, is irreversible, has high enthalpy, and is specific.

  7. State the periodic trends in atomic radius across a period and down a group.

    Atomic radius decreases across a period (increasing nuclear charge) and increases down a group (added shells).

  8. How do ionization enthalpy and electronegativity vary across a period?

    Both ionization enthalpy and electronegativity generally increase across a period from left to right, due to increasing effective nuclear charge and decreasing atomic size.

  9. State VSEPR theory and predict the shape of a molecule with 4 bonding pairs and no lone pairs.

    VSEPR theory states that electron pairs around a central atom arrange to minimize repulsion. Four bonding pairs with no lone pairs give a tetrahedral shape (109.5 degrees), e.g., CH4.

  10. Define hybridization and give the geometry for sp, sp2, and sp3.

    Hybridization is the mixing of atomic orbitals to form equivalent hybrid orbitals. sp = linear (180 degrees), sp2 = trigonal planar (120 degrees), sp3 = tetrahedral (109.5 degrees).

  11. What is the bond order formula in molecular orbital theory?

    Bond order = (number of bonding electrons - number of antibonding electrons) / 2.

  12. Distinguish between sigma and pi bonds.

    A sigma bond forms by head-on (axial) overlap of orbitals and is stronger; a pi bond forms by sidewise (lateral) overlap of p-orbitals and is weaker. Single bonds are sigma; double/triple bonds contain pi bonds.

  13. Why does the s-block contain alkali and alkaline earth metals, and what is their general reactivity?

    The s-block has groups 1 (alkali metals, ns1) and 2 (alkaline earth metals, ns2). They are highly reactive, electropositive metals; reactivity increases down each group.

  14. What is the diagonal relationship, with an example from the s-block?

    Certain elements in period 2 resemble the element diagonally placed in period 3, group adjacent. Example: lithium resembles magnesium, and beryllium resembles aluminium.

  15. Why is the +1 oxidation state increasingly stable down group 13 and 14 (inert pair effect)?

    The inert pair effect: the ns2 electrons become reluctant to participate in bonding down the group due to poor shielding by d and f electrons, stabilizing a lower oxidation state (e.g., Tl+1, Pb+2).

  16. Define transition elements and explain why they show variable oxidation states.

    Transition (d-block) elements have partially filled d-orbitals in atoms or common ions. They show variable oxidation states because the energies of (n-1)d and ns electrons are similar, so both can be lost.

  17. Why are most transition metal compounds coloured?

    Because of d-d electronic transitions: when d-orbitals split in a ligand field, electrons absorb visible light to jump between d levels, and the complementary colour is transmitted.

  18. What are lanthanoid contraction and its consequence?

    Lanthanoid contraction is the steady decrease in atomic/ionic size across the lanthanoid series due to poor shielding by 4f electrons. It causes second- and third-row transition elements (e.g., Zr and Hf) to have similar sizes.

  19. State Werner's coordination theory in brief.

    Metals show two valencies: primary (ionizable, satisfied by anions) and secondary (non-ionizable, satisfied by ligands, equal to coordination number). Secondary valencies are directional and fix the geometry.

  20. State the rule for naming the coordination sphere and give the formula meaning of [Co(NH3)6]Cl3.

    Ligands are named alphabetically before the metal, with the metal's oxidation state in Roman numerals. [Co(NH3)6]Cl3 is hexaamminecobalt(III) chloride: Co3+ with six ammine ligands, coordination number 6.

  21. What is crystal field splitting in an octahedral complex?

    In an octahedral field the five degenerate d-orbitals split into a lower t2g set (dxy, dyz, dxz) and a higher eg set (dx2-y2, dz2), separated by the crystal field splitting energy (delta_o).

  22. State Markovnikov's rule for addition of HX to an unsymmetrical alkene.

    The negative part (X) of the reagent adds to the carbon bearing fewer hydrogen atoms, while H adds to the carbon with more hydrogens, giving the more stable carbocation intermediate.

  23. Define and order the stability of carbocations.

    A carbocation is a positively charged carbon species. Stability order: tertiary > secondary > primary > methyl, due to increasing hyperconjugation and the +I (inductive) effect of alkyl groups.

  24. Distinguish between SN1 and SN2 reaction mechanisms.

    SN1 is two-step via a carbocation, first-order kinetics, favoured by tertiary substrates, and gives racemization. SN2 is one-step concerted, second-order kinetics, favoured by primary substrates, and proceeds with inversion of configuration.

  25. What is Markovnikov's anti rule (peroxide/Kharasch effect)?

    In the presence of peroxides, HBr adds to an unsymmetrical alkene against Markovnikov's rule (anti-Markovnikov) via a free-radical mechanism, placing Br on the carbon with more hydrogens.

  26. Name the reactions for: (a) aldehyde/ketone + HCN, and (b) two molecules of aldehyde under dilute base.

    (a) Nucleophilic addition forming a cyanohydrin. (b) Aldol condensation, giving a beta-hydroxy aldehyde/ketone that can dehydrate to an alpha,beta-unsaturated carbonyl.

  27. What is the difference between an aldehyde and a ketone in terms of structure and oxidation?

    An aldehyde has the carbonyl carbon bonded to at least one H (R-CHO) and is easily oxidized to a carboxylic acid. A ketone has the carbonyl carbon bonded to two carbons (R-CO-R') and resists mild oxidation.

  28. Describe the Hofmann bromamide degradation reaction.

    A primary amide is treated with Br2 and aqueous (or alcoholic) KOH/NaOH to give a primary amine with one fewer carbon atom: R-CONH2 to R-NH2.

  29. Differentiate addition polymers from condensation polymers with one example each.

    Addition polymers form by repeated addition of monomers with no by-product (e.g., polythene from ethene). Condensation polymers form by combination of monomers with loss of a small molecule like water (e.g., nylon-6,6).

  30. Name the four major classes of biomolecules and their building blocks.

    Carbohydrates (monosaccharides), proteins (amino acids), nucleic acids (nucleotides), and lipids (fatty acids and glycerol).

  31. What are essential and non-essential amino acids?

    Essential amino acids cannot be synthesized by the body and must be obtained from the diet; non-essential amino acids can be synthesized within the body.

  32. Distinguish between BOD and COD as water-quality indicators.

    BOD (Biochemical Oxygen Demand) is the oxygen used by microorganisms to decompose organic matter biologically. COD (Chemical Oxygen Demand) is the oxygen required to chemically oxidize all organic/inorganic matter; COD is usually higher than BOD.

  33. Define green chemistry and one of its core goals.

    Green chemistry is the design of chemical products and processes that reduce or eliminate the use and generation of hazardous substances; a core goal is preventing waste rather than treating it after formation.

  34. How does Lassaigne's test detect nitrogen in an organic compound?

    The compound is fused with sodium to convert nitrogen to sodium cyanide (NaCN); adding ferrous sulphate and ferric ions produces Prussian blue (ferric ferrocyanide), confirming nitrogen.

  35. On what principle does chromatography separate components of a mixture?

    Differential distribution (adsorption or partition) of components between a stationary phase and a moving mobile phase, so components travel at different rates and separate.

AFMC / NEET-linked AFMC Admission Chemistry (NEET-UG Academic Component) FAQ

What is in the AFMC / NEET-linked AFMC Admission Chemistry (NEET-UG Academic Component) syllabus?

AFMC / NEET-linked AFMC Admission Chemistry (NEET-UG Academic Component) is split into 4 chapters: Physical Chemistry, Inorganic Chemistry, Organic Chemistry and Applied and Everyday Chemistry. Together they contain 19 topics and 46 sub-topics.

How many chapters are in AFMC / NEET-linked AFMC Admission Chemistry (NEET-UG Academic Component)?

4 chapters, containing 19 topics and 46 sub-topics. The largest chapter is Physical Chemistry, with 6 topics.

Are there flashcards for AFMC / NEET-linked AFMC Admission Chemistry (NEET-UG Academic Component)?

Yes — a 55-card Chemistry (NEET-UG Academic Component) deck, printed in full in the flashcards section of this page and available in the Examius app with spaced repetition. The free plan covers one exam of your choice, including its flashcards; Examius Pro, a one-time purchase, unlocks every other exam and deck.