When 2,2-dimethylcyclohexanol is treated with acid,1,2-dimethylcyclohexene and iso-propylidenecyclopentane are the products obtained. Draw a detailed mechanism thatexplains this result.CH 3CH3CH3H3O*CH3OHCH3CH31,2-dimethyl-isopropylidene-cyclopentane2,2-dimethyl-cyclohexanolcyclohexene

The details mechanism is given below.Explanation:

Answered: When 2,2-dimethylcyclohexanol is…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...

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