The {S_{N}2} reaction of an asymmetric carbon | vedclass

Name: Exam Paper Generator | JEE NEET Paper Generator | Vedclass
Brand: Vedclass
Rating: 5 (35 reviews)

Question

(B) The ${S_{N}2}$ mechanism involves a backside attack by the nucleophile on the electrophilic carbon atom.This process results in the inversion of c

Vedclass · Accepted Answer

$A$ product with inverted optical rotation

Vedclass · Answer

(B) The ${S_{N}2}$ mechanism involves a backside attack by the nucleophile on the electrophilic carbon atom.This process results in the inversion of configuration at the chiral center,which is known as the $Walden$ inversion.Therefore,if the starting material is optically active,the product will have the opposite configuration,leading to a product with inverted optical rotation.

The ${S_{N}2}$ reaction of an asymmetric carbon compound always gives:

Similar Questions

The hydrolysis of $2$-bromo-$3$-methylbutane by the $S_N1$ mechanism primarily yields:

Which of the following will undergo $S_{N}2$ reaction most rapidly?

The product of which of the following reactions undergoes hydrolysis by the $S_N 1$ mechanism?

Which of the following alkyl halides is used as a methylating agent?

Which of the following expressions is representative of the rate law for a $S_{N}2$ reaction?

Vedclass Test Series

Exam Paper Generator

Online Exam Module