Question: When optically active (S)-2-methylcyclopentanone is treated with aqueous base, the compoundloses its optical activity. Explain this observation, and draw a mechanism that shows how racemization
When optically active (S)-2-methylcyclopentanone is treated with aqueous base, the compoundloses its optical activity. Explain this observation, and draw a mechanism that shows how racemization occurs.
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Deprotonation at the carbon changes the hybridization ... View full answer
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