Which of the following is the most stable for | vedclass

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

Question

(C) The given structure is a primary carbocation: $CH_3-C(CH_3)_2-CH_2^{\oplus}$.Carbocations undergo rearrangement to form more stable carbocations (

Vedclass · Accepted Answer

$CH_3-C^{\oplus}(CH_3)-CH_2-CH_3$

Vedclass · Answer

(C) The given structure is a primary carbocation: $CH_3-C(CH_3)_2-CH_2^{\oplus}$.Carbocations undergo rearrangement to form more stable carbocations (tertiary > secondary > primary).$A$ $1,2$-hydride shift occurs from the adjacent carbon to the positively charged carbon.This results in the formation of a tertiary carbocation: $CH_3-C^{\oplus}(CH_3)-CH_2-CH_3$.This tertiary carbocation is more stable due to hyperconjugation and inductive effects.

Which of the following is the most stable form for the given structure after rearrangement?

Similar Questions

Arrange the following carbocations in the correct order of stability:

Represent the structure of the free radical,carbocation,and carbanion derived from methane.

The product of the rearrangement of the given oxyallyl cation is:

What is the hybridisation state of the benzyl carbocation shown in the image?

The most stable carbanion among the following is

Vedclass Test Series

Exam Paper Generator

Online Exam Module