Treatment of an aldehyde or ketone with cyanide ion (: C N), followed by proton-ation of

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Treatment of an aldehyde or ketone with cyanide ion (–: C ≡ N), followed by proton-ation of the tetrahedral alkoxide ion intermediate, gives a cyanohydrins. Show the structure of the cyanohydrins obtained from Cyclohexanone.

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Organic Chemistry

ISBN: 9780495112587

7 Edition

Authors: John McMurry

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Question Posted: Feb 23, 2011 05:52 AM

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Treatment of an aldehyde or ketone with cyanide ion (: C N), followed by proton-ation of

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O CN O CN 133 H2O protonation of cyanohydrin tetrah...View the full answer

Organic Chemistry

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