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15.1.7—Rate of hydrolysis of halogenoalkanes

Syllabus
9701–2028–2029
Objective
15.1.7
Level
AS

Hydrolysis rates reflect C–X bond strength and substitution pathway

In hydrolysis, water or hydroxide replaces X in a halogenoalkane. A weaker C–X bond generally hydrolyses more readily, and aqueous silver nitrate detects the halide ion formed as AgX.

Keep the test fair: same concentration, temperature, solvent and volume. The precipitate time is evidence about relative rate, not a direct measurement of bond energy alone.

Iodoalkanes usually form AgI more quickly than bromo- or chloroalkanes because C–I cleavage is easier. The precipitate colour helps identify the halide.

A faster precipitate does not prove the reaction is purely SN1; substrate structure and nucleophile conditions also affect the rate.

ConceptA-Level CAIE Chemistry AS