MolSynapsequestion bank
MolSynapse / Question bank / Organic Reaction Mechanisms III: Nucleophilic Substitution / SN1 mechanism, rate, stereochemistry, rearrangement
NEET levelSingle correct optionDifficulty 1 of 3o3010

In aqueous acetone, solvolyses by SN1. When some is added to the solution, the observed rate of solvolysis

  1. Adecreases slightly (common-ion effect)
  2. Bincreases markedly
  3. Cremains exactly unchanged under all conditions
  4. Dbecomes second order in the substrate

Answer: A

The ionisation is reversible. Added chloride ion pushes the equilibrium back (and captures the cation), so fewer cations are converted to product and the net rate falls slightly. This is the common-ion (mass-law) effect typical of stable carbocations.
Practice Organic Reaction Mechanisms III: Nucleophilic Substitution More on SN1 mechanism, rate, stereochemistry, rearrangement

More questions on SN1 mechanism, rate, stereochemistry, rearrangement