The detailed mechanism for the given reaction of formation of cyclic ether is to be drawn. Concept introduction: The electrophilic addition reaction of an alkene occurs through formation of a more stable carbocation. The electrophilic addition of water across the double bond in an acidic condition produces the alcohol product. The reaction proceeds with proton transfer reaction to form a stable carbocation, followed by the action of water as a nucleophile. Cyclic ethers are formed when the single substrate has both alkene as well as alcoholic functional group that can form a stable cyclic structure.

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Chapter 11, Problem 11.36P

Interpretation Introduction

Interpretation:

The detailed mechanism for the given reaction of formation of cyclic ether is to be drawn.

Concept introduction:

The electrophilic addition reaction of an alkene occurs through formation of a more stable carbocation. The electrophilic addition of water across the double bond in an acidic condition produces the alcohol product. The reaction proceeds with proton transfer reaction to form a stable carbocation, followed by the action of water as a nucleophile. Cyclic ethers are formed when the single substrate has both alkene as well as alcoholic functional group that can form a stable cyclic structure.

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