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Hydrohalogenation gives the corresponding vinyl halides or alkyl dihalides, again depending on the number of equivalents of HX added.
The addition of water to alkynes is a related reaction except the initial enol intermediate converts to the ketone or aldehyde.
Illustrative is the hydration of phenylacetylene gives acetophenone, and the ( Ph < sub > 3 </ sub > P ) AuCH < sub > 3 </ sub >- catalyzed hydration of 1, 8-nonadiyne to 2, 8-nonanedione:

1.923 seconds.