An `SN^(2)` reaction at on asymmetric carbon atom of a compound always givesA. an enantiomers of a substrateB. a product with same optical rotationC. a mixture of diastereoisomersD. a single stereoisomers

An `SN^(2)` reaction at on asymmetric carbon atom of a compound always

1.	An `SN^(2)` reaction at on asymmetric carbon atom of a compound always givesA. an enantiomers of a substrateB. a product with same optical rotationC. a mixture of diastereoisomersD. a single stereoisomers
Answer» Correct Answer - D In `SN^(2)` reaction , inverstion of configureation occurs. Since the reactant and the product are not enatiomers, therefore, the sign of optical rotation may on may not be changed and hencesingle stereoisomer is obtained.

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An `SN^(2)` reaction at on asymmetric carbon atom of a compound always givesA. an enantiomers of a substrateB. a product with same optical rotationC. a mixture of diastereoisomersD. a single stereoisomers

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