MCQ
Which of the following carbocation is most stable?
  • A
    $\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ + \\ (\text{CH}_3)_3\text{C}.\text{CH}_2$
  • $\ \ \ \ \ \ \ \ \ \ \ + \\ (\text{CH}_3)_3\text{C}$
  • C
    $\ \ \ \ \ \ \ \ \ \ \ \ \ \ + \\ \text{CH}_3\text{CH}_2\text{CH}_2$
  • D
    $\ \ \ \ \ \ \ + \\ \text{CH}_3 \text{CH CH}_2\text{CH}3$

Answer

Correct option: B.
$\ \ \ \ \ \ \ \ \ \ \ + \\ (\text{CH}_3)_3\text{C}$
$\ \ \ \ \ \ \ \ \ \ \ + \\ (\text{CH}_3)_3\text{C}$ is a tertiary carbocation. A tertiary carbocation is the most stable carbocation due to the electron releasing effect of three methyl groups. An increased $+\ I$ effect by three methyl groups stabilizes the positive charge on the carbocation.

Need a full question paper?

Generate a complete, print-ready paper with questions like this in minutes — across 16+ boards, with answer keys.

Start Generating Free