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sp2606 [1]
3 years ago
11

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

Chemistry
1 answer:
DENIUS [597]3 years ago
4 0

Answer:

methyl tert-butyl ether is produced as a product

Explanation:

  • Nucleophilic substitution in solvolysis reaction of tert-butyl bromide goes through S_{N}1 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.

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