Question: H2OCat.HCl Basic: Provide a reasonable stepwise mechanism for the transformation using curved arrow formalism. Master: If enantioenriched ketone is used in this reaction, the resulting

H2OCat.HCl Basic: Provide a reasonable stepwise mechanism for the transformation using

H2OCat.HCl Basic: Provide a reasonable stepwise mechanism for the transformation using curved arrow formalism. Master: If enantioenriched ketone is used in this reaction, the resulting acetal is produced as a racemic mixture. Provide a mechanistic explanation for this observation. A satisfactory answer will require the drawing of the responsible elementary mechanistic steps

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