Treatment of an aldehyde or ketone with cyanide ion
Chapter 19, Problem 19(choose chapter or problem)
Treatment of an aldehyde or ketone with cyanide ion \(\left(^{-}: C \equiv N\right)\), followed by protonation of the tetrahedral alkoxide ion intermediate, gives a cyanohydrin. Show the structure of the cyanohydrin obtained from cyclohexanone.
Equation Transcription:
Text Transcription:
\left(^{-}: C \equiv N\right)
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