In which of the following compounds,the $C-Cl$ bond ionization shall give the most stable carbocation?

  • A
    $tert$-Butyl chloride: $(CH_3)_3C-Cl$
  • B
    $1$-Phenylethyl chloride: $C_6H_5-CH(CH_3)-Cl$
  • C
    $2$-Nitroethyl chloride: $O_2N-CH_2-CH_2-Cl$
  • D
    Isopropyl chloride: $(CH_3)_2CH-Cl$

Explore More

Similar Questions

$S_N^1$ and $S_N^2$ reactions are

The reaction of ethyl bromide with lead-sodium alloy gives ......... .

Difficult
View Solution

Which of the following compounds has a chiral carbon atom?

Consider the following bromides.
The correct order of $S_N1$ reactivity is

Consider the given reaction: $CH_3-CH=CH-CH_2-OH \xrightarrow[S_N1]{HBr} [P]$. In the given reaction,the product $[P]$ is:

Difficult
View Solution

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