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Chapter 9: Q15P (page 404)

What is the product of the reaction of bromoethane with each of the following nucleophiles?

Short Answer

Expert verified

The products of the reactions are given below,

Step by step solution

01

Definition of SN2 reaction

SN2 reaction is a nucleophilic substitution reaction where the Nucleophilic attack and bond breaking between carbon and electronegative group happens simultaneously through a 5 coordinated transition state. In this reaction, the rate equation is second order having both the concentration of nucleophile and alkyl bromide.

02

Mechanism of SN2 reaction

The mechanism of SN2 reaction is given below on a hypothetical reaction.

OH- =nucleophile

03

Product of the reactions

The SN2 reaction occurs between bromoethane and all the nucleophiles given above. All of them formed the products, maintaining the above reaction mechanism. The products are given below.

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Most popular questions from this chapter

a. Which reacts faster in an E2 reaction: 3-bromocyclohexene or Bromo cyclohexane?

b. Which reacts faster in an E1 reaction?

Propose a mechanism for the following reaction:

a. Explain why 1-bromo-2,2-dimethylpropane has difficulty undergoing both SN2 and SN1 reactions.

b. Can it undergo E2 and E1 reactions?

Question:What product is formed when 1-bromopropane reacts with each of the following nucleophiles?

a. HO-

b. -NH2

c. CH3S-

d. HS-

e. CH3O-

f. CH3NH2

Draw the substitution and elimination products for the following reactions, showing the configuration of each product:

a. trans-1-chloro-2-methylcyclohexane + CH3O-

b. cis-1-chloro-2-methylcyclohexane + CH3O鈭�

c. 1-chloro-1-methylcyclohexane + CH3O-

d. 1-chloro-1-methylcyclohexane + CH3OH
See all solutions

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