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in Chemistry by (138k points)
Explain the mechanism of the following reactions:
(i) Addition of Grignard’s reagent to the carbonyl group of a compound forming an adduct followed by hydrolysis.
(ii) Acid catalysed dehydration of an alcohol forming an alkene.
(iii) Acid catalysed hydration of an alkene forming an alcohol.

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1 Answer

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(i) Step I: Nucleophilic addition of Grignard reagent to Carbonyl group.

Step II: Formation of carbocation: It is the slowest step and hence, the rate determining step.

To drive the equilibrium to the right, ethylene is removed as it is formed.

Mechanism
Step I: Protonation of alkene to form carbocation by electrophilic attack of H3O+.

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