Hydrolysis of alkyl iso cynide full process explanation
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A novel mechanism for acid-catalyzed hydrolysis of cyclohexyl isocyanide is proposed. It is specific acid/general base catalysis, involving a fast, pre-equilibrium C-protonation of the isocyanide, followed by a rate-determining attack of water on the electron-deficient carbon of the protonated isocyanide. The pKa of N-cyclohexylnitrilium ion was determined to be 0.86±0.05.
Acid-catalyzed hydrolysis of the isocyanide is specific-acid/general-base catalysis.

Acid-catalyzed hydrolysis of the isocyanide is specific-acid/general-base catalysis.

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