Part of JPC-06 — Chemical Kinetics: Rate Laws & Arrhenius Equation

JEE Strategy for Chemical Kinetics

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Chemical kinetics contributes ~4% of JEE Main marks. High-yield topics: (1) First-order calculations — master k = 2.303t\frac{2.303}{t}log(aax\frac{a}{a-x}), t1t_1/2 = 0.693/k, fraction remaining = 12\frac{1}{2}^n. These appear almost every year. (2) Arrhenius equation — lnk2k1\frac{k2}{k1} = EaR\frac{Ea}{R}(1/T1 - 1/T2) for Ea calculation. Know R = 8.314 Jmol.K\frac{J}{mol.K}, convert kJ to J. (3) Order determination from initial rates data — systematic comparison of experiments. (4) Gas-phase pressure problems — write PAP_A in terms of P0P_0 and PtP_t correctly. Common mistakes: (a) confusing molecularity with order, (b) using stoichiometric coefficients as orders for complex reactions, (c) forgetting to convert Ea from kJ to J in Arrhenius calculations, (d) sign errors in 1/T1 - 1/T2, (e) using wrong log base (ln vs log — factor of 2.303). Quick checks: k must have correct units for the order. First-order half-life is independent of concentration. Rate always decreases with time (except zero order where it stays constant). A catalyst changes k but not KeqK_{eq}.

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