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How might you prepare each of the following molecules using a nucleophilic substitution reaction at some step?

Short Answer

Expert verified

CH3Br + −O−CCH33 → CH3−O−CCH33 + NaBr

CH3OH + Cl−CCH33 → CH3−O−CCH33 + CH33C=CH2

Step by step solution

01

SN2reaction

It is a nucleophilic substitution reaction in which an old bond is broken and new bond is formed both processes occur simultaneously. Hence, it’s a single-step reaction.

The two reacting species are involved in the rate determining steps.

CH3Br + −O−CCH33 → CH3−O−CCH33 + NaBr

Substitution reaction

02

E2reaction

It is a nucleophilic elimination reaction in which an old bond is broken and new bond is formed both the process occur simultaneously and no intermediate is formed.

Here, the carbon-hydrogen or halogen bond breaks to form a new double bond. Hence, it’s a single-step reaction.

CH3OH + Cl−CCH33 → CH3−O−CCH33 + CH33C=CH2

Elimination reaction

03

Formation of CH3-O-CCH33

Here, the nucleophilic substitution occur where NaBr is produced and desired product is formed.

The two reacting species are involved in the rate determining steps.

CH3Br + −O−CCH33 → CH3−O−CCH33 + NaBr

Substitution reaction

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