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

methyl tert-butyl ether is produced as a product

Explanation:

Nucleophilic substitution in solvolysis reaction of tert-butyl bromide goes through mechanism.Because Br is a good leaving group due to it's large size and high polarizability and methanol is an weak nucleophile.In the first step, tert-butyl cation is produced. In the second step, methanol attacks the carbocation and produce methyl tert-butyl ether after deprotonation.Reaction and structure of product has been shown below.