Chemistry, 27.04.2021 15:10, alyssatamayo641
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. Collapse question part 21.55a Get help answering Molecular Drawing questions Get help answering Molecular Drawing questions. Draw (S)-2-methylcyclopentanone.
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When optically active (S)-2-methylcyclopentanone is treated with aqueous base, the compound loses it...
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