Water is added to an alkene during an acid-catalyzed hydration reaction to create alcohol: A sequential mechanism for the reaction begins with the protonation of the double bond.
Alcohol is produced when alkenes are hydrated with acid in accordance with Markownikoff's rule. Alkenes can also be converted into alcohols by the processes of hydroboration oxidation and oxy-mercuration-de-mercuration.
Water adds to alkenes only in the presence of an acid catalyst, resulting in the production of alcohol. However, there are two significant drawbacks to the acid-catalyzed hydration: Arrangements may change. Regioselectivity is unpredictable.
Hydration is the process of adding water to alkenes on a net basis. The pi bond in the alkene and the OH bond in the water are broken as a result, and a C-H bond and a C-OH bond are formed. Typically, the reaction is exothermic by 10 to 15 kcal/mol1, although the entropy change is between -35 and -40.
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