Addition of bromine to 1,3-butadiene gives | vedclass

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

Question

(C) The electrophilic addition of bromine to $1,3-$butadiene proceeds through the formation of a resonance-stabilized allylic carbocation intermediate

Vedclass · Accepted Answer

Both $1,2-$ and $1,4-$addition products

Vedclass · Answer

(C) The electrophilic addition of bromine to $1,3-$butadiene proceeds through the formation of a resonance-stabilized allylic carbocation intermediate. This intermediate can be attacked by the bromide ion at the $C-2$ position to form the $1,2-$addition product ($3,4-$dibromobut-$1-$ene) or at the $C-4$ position to form the $1,4-$addition product ($1,4-$dibromobut-$2-$ene). Therefore,both $1,2-$ and $1,4-$addition products are formed.

Addition of bromine to $1,3-$butadiene gives

Similar Questions

Explain the dehalogenation of vicinal dihalides with an example.

What is the product of the following reaction?

The compound most likely to decolourize a solution of potassium permanganate is

$1, 2$-dibromocyclohexane on dehydrohalogenation gives

When vinyl and allyl radicals are joined together,we get:

Vedclass Test Series

Exam Paper Generator

Online Exam Module