Assertion $(A)$: $S_N1$ hydrolysis of optically active $2-$bromooctane results in the formation of $(\pm)-$octan$-2-$ol.
Reason $(R)$: The reaction proceeds through a planar carbocation which can be attacked by the nucleophile from either side.
The correct answer is

  • A
    $(A)$ and $(R)$ are correct,$(R)$ is the correct explanation of $(A)$
  • B
    $(A)$ and $(R)$ are correct but $(R)$ is not the correct explanation of $(A)$
  • C
    $(A)$ is correct but $(R)$ is not correct
  • D
    $(A)$ is not correct but $(R)$ is correct

Explore More

Similar Questions

Which one of the following is chiral?

The $S_{N}2$ reaction mechanism proceeds through ........

Difficult
View Solution

Ethyl bromide reacts with lead-sodium alloy to form

Iodoform gives a precipitate with $AgNO_3$ on heating,but chloroform does not because ..........

Difficult
View Solution

Identify the most suitable reagents $(I)$ and $(II)$ for the following sequence of reactions:

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo