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Chemical Kinetics

Class 12

15 previous-year questions from this chapter every option and the correct answer, free · where the marks are

1. Rate law, order and molecularity

Exam focus: Order is an experimentally determined exponent in the rate law — it can be zero, fractional, even negative — while molecularity is a theoretical count of colliding species in one elementary step and must be a positive integer; the two coincide only for a genuine single-step reaction. You cannot read a complex, multi-step reaction's rate law off its balanced equation the way you can for an elementary step.

Rate Law, Order and Molecularity

Physics Wallah - Alakh Pandey

Directly covers the rate-law expression and order of reaction.

2. Integrated rate equations and half-life

Exam focus: First-order half-life (t½ = 0.693/k) doesn't depend on starting concentration — the signature fact used to identify first order from a data table. Zero-order half-life is the opposite: directly proportional to initial concentration (t½ = [A]₀/2k), and mixing up which order does which is the standard trap.

First-Order Kinetics: Integrated Rate Law and Half-Life

Physics Wallah - Alakh Pandey

Thorough treatment of the first-order integrated rate equation and half-life (the higher-weightage case for NEET); zero-order integrated rate law/half-life is covered in a separate, companion lecture, not this one.

3. Arrhenius equation and activation energy

Exam focus: A catalyst speeds up a reaction by lowering the activation energy through an alternate pathway — it doesn't change ΔH, and because it accelerates the forward and reverse reactions equally, it never shifts the equilibrium position or the value of K. That "catalysts don't touch equilibrium, only kinetics" point is a recurring assertion-reason question.

Arrhenius Equation and Activation Energy

Physics Wallah - Alakh Pandey

Covers the Arrhenius equation, activation energy and the temperature dependence of rate directly.