Chemistry, 27.05.2020 01:59 montana53

When optically active (S)-2-methylcyclopentanone is treated with aqueous base, the compound loses its optical activity. Explain this observation and draw a mechanism that shows how racemization occurs. For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph.

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When optically active (S)-2-methylcyclopentanone is treated with aqueous base, the compound loses it...

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