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Starting from cyclohexanol, show how to prepare:
Show all reagents and molecules synthesized along the way after each step. You do not have to use curved arrows.
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- Which of these are optically active?a: Is the product chiral? _____ b: Assuming that the reaction takes place with equal likelihood from both Re and Si faces of the carbonyl group, is the product optically active? ____Please help me complete and indicate if the product is a meso, enantioner or racemic mixture