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14.2.2—Reactions of alkenes

Syllabus
9701–2028–2029
Objective
14.2.2
Level
AS

Electrophilic addition across an alkene depends on the reagent and conditions

The electron-rich C=C attacks an electrophile, then a nucleophile bonds to the carbocation-like intermediate. Hydrogenation adds H₂ with Pt/Ni, hydration adds steam with phosphoric acid, and HX adds a hydrogen halide at room temperature.

The π bond is consumed and each alkene carbon gains a new atom or group. Write the reagent, catalyst and product rather than treating every addition as hydrogenation.

CH₂=CH₂ + H₂ → CH₃CH₃; CH₂=CH₂ + H₂O ⇌ CH₃CH₂OH with H₃PO₄. Both use the same alkene but different reagents and products.

Electrophilic addition is not substitution, and steam hydration is reversible whereas catalytic hydrogenation is not described by the same equilibrium.

ConceptA-Level CAIE Chemistry AS