which reacts slower with naoh cis-2-bromocyclohexanol or (1R,2R)-2-bromocyclohexanol, due to stereochemistry and why

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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which reacts slower with naoh cis-2-bromocyclohexanol or (1R,2R)-2-bromocyclohexanol, due to stereochemistry and why

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