Subjects
Sections | |||
---|---|---|---|
Addition Reaction | 7 mins | 0 completed | Learn |
Markovnikov | 5 mins | 0 completed | Learn |
Hydrohalogenation | 7 mins | 0 completed | Learn Summary |
Acid-Catalyzed Hydration | 17 mins | 0 completed | Learn Summary |
Oxymercuration | 20 mins | 0 completed | Learn Summary |
Hydroboration | 27 mins | 0 completed | Learn Summary |
Hydrogenation | 7 mins | 0 completed | Learn |
Halogenation | 6 mins | 0 completed | Learn Summary |
Halohydrin | 17 mins | 0 completed | Learn Summary |
Carbene | 13 mins | 0 completed | Learn Summary |
Epoxidation | 8 mins | 0 completed | Learn Summary |
Epoxide Reactions | 9 mins | 0 completed | Learn Summary |
Dihydroxylation | 9 mins | 0 completed | Learn Summary |
Ozonolysis | 7 mins | 0 completed | Learn Summary |
Ozonolysis Full Mechanism | 25 mins | 0 completed | Learn |
Oxidative Cleavage | 8 mins | 0 completed | Learn Summary |
Alkyne Oxidative Cleavage | 6 mins | 0 completed | Learn Summary |
Alkyne Hydrohalogenation | 3 mins | 0 completed | Learn Summary |
Alkyne Halogenation | 2 mins | 0 completed | Learn Summary |
Alkyne Hydration | 6 mins | 0 completed | Learn Summary |
Alkyne Hydroboration | 3 mins | 0 completed | Learn Summary |
Predict the product for the reaction below.
We’re being asked to determine the product for the given reaction.
Recall that alkynes are converted to vinyl alcohols (an enol) via either acid-catalyzed hydration or oxymercuration:
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