In an S_N2 reaction on a chiral carbon atom,w | vedclass

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(D) The $S_N2$ mechanism involves a backside attack by the nucleophile on the chiral carbon atom.This leads to the inversion of configuration,also kno

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$A$ single stereoisomer

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(D) The $S_N2$ mechanism involves a backside attack by the nucleophile on the chiral carbon atom.This leads to the inversion of configuration,also known as the $Walden$ inversion.Since the nucleophile attacks from the side opposite to the leaving group,the spatial arrangement of the atoms around the chiral center is inverted.Therefore,the product formed is a single stereoisomer with an inverted configuration relative to the reactant.

In an $S_N2$ reaction on a chiral carbon atom,what is always produced?

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