Rate of Reaction and Rate Laws

Chemical Kinetics • Class 12 Chemistry • NCERT • CBSE

Rate of reaction = change in concentration/time. Rate law: r = k[A]ˣ[B]ʸ. Zero-order: t½ = [A₀]/2k. First-order: t½ = 0.693/k (constant). Arrhenius equation: k = Ae^(−Ea/RT). Activation energy Ea from slope of ln k vs 1/T graph.

Key Formulas

Frequently Asked Questions

What is the difference between order and molecularity of a reaction?
Order: experimentally determined exponent sum in rate law (r = k[A]ˣ[B]ʸ); can be 0, 1, 2, fraction, negative; refers to overall reaction. Molecularity: number of molecules actually participating in an elementary step; always a positive integer (1, 2, or 3); applies to elementary reactions only. Order = molecularity only for simple one-step reactions.
Why is half-life of a first-order reaction independent of initial concentration?
For first-order: t½ = 0.693/k. The rate constant k depends only on temperature, not concentration. Therefore t½ is constant regardless of initial concentration. This is a unique property of first-order reactions. Example: radioactive decay is first-order — each isotope has a characteristic constant half-life.
How does a catalyst work?
A catalyst provides an alternate reaction pathway with lower activation energy (Ea). With lower Ea, more molecules in the Boltzmann distribution have sufficient energy to react → reaction rate increases. The catalyst is not consumed overall (though it participates in intermediate steps). It affects both forward and reverse rates equally, so equilibrium position remains unchanged.

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