Draw a structure for the product of nucleophilic substitution obtained on solvolysis of tert−butyl bromide in methanol, and arra

Question

Blababa [14]

4 years ago

10

Draw a structure for the product of nucleophilic substitution obtained on solvolysis of tert−butyl bromide in methanol, and arra

nge the correct mechanism for its formation. Be sure to answer all parts.

Chemistry

1 answer:

Elena-2011 [213] · Answer 1 · 2021-11-14T16:57:07+03:00

Answer:

2-methoxy-2-methylpropane

Explanation:

The first step for this reaction is the carbocation formation. In this step, a tertiary carbocation is formed. Also, we will have a good leaving group so bromide will be formed. Then the methanol acts as a nucleophile and attacks the carbocation. Next, a positive charge is generated upon the oxygen, this charge can be removed when the hydrogen leaves the molecule as $H^+$ . (See figure)