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6. When cyclohexene is treated with m-chloroperbenzoic acid and water, trans-cyclohexane-1,2-diol is produced. Propose a complete, detailed, reasonable mechanism (arrow pushing) for this reaction. The

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6. When cyclohexene is treated with m-chloroperbenzoic acid and water, trans-cyclohexane-1,2-diol is produced. Propose a complete, detailed, reasonable mechanism (arrow pushing) for this reaction. The mechanism should account for the observed stereochemistry. The mechanism should be rooted in class materials from lecture/textbook

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