In an S_N1 reaction on chiral centres,there i | vedclass

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(A) The $S_N1$ reaction proceeds via the formation of a planar carbocation intermediate. Since the nucleophile can attack from either side of the plan

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inversion more than retention leading to partial racemisation

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(A) The $S_N1$ reaction proceeds via the formation of a planar carbocation intermediate. Since the nucleophile can attack from either side of the planar carbocation,a racemic mixture is formed. However,because the leaving group partially blocks the front side (ion-pair effect),the attack from the back side is slightly favored. Therefore,there is inversion more than retention,leading to partial racemisation.

In an $S_N1$ reaction on chiral centres,there is

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