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Answer: Salient features of SN1 (unimolecular nucleophilic substitution):

  1. It is a first order reaction: rate = k[RX]; the rate depends only on the concentration of the substrate.
  2. It takes place in two steps. Step 1 (slow, rate-determining): the C–X bond ionises to form a planar carbocation intermediate. Step 2 (fast): the nucleophile attacks the carbocation.
  3. Because the carbocation is planar, the nucleophile can attack from either side; an optically active substrate gives a racemic mixture (racemisation).
  4. Reactivity order: 3° > 2° > 1° > CH3X (stability of carbocation); polar protic solvents favour the reaction.
Doubtly AI · 29 Oct 2026 AI-verified · Nov 2026 Report
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