Hydroboration

Hydroboration Hydroboration Definition: Hydroboration is the treatment of alkynes with BH3, followed by H2O2 in which aldehydes and ketones are obtained. Hydroboration Explained: Hydroboration is a two-step reaction sequence which proceeds via an anti-Markovnikov addition where installing a hydroxyl group at…

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Hydrate formation [H2O]

Hydrate formation [H2O] Hydrate formation [H2O] Definition: Treatment of a carbonyl compound with H2O in the presence of acid or base catalyst adds the elements of H and OH across the carbonyl bond, forming a gem-diol or hydrate. Hydrate formation [H2O] Explained: The…

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Hofmann rearrangement

Hofmann rearrangement Hofmann Rearrangement Definition: When amides are treated with halide and base, a rearrangement occurs, resulting in the loss of carbon dioxide and the formation of an amine. Hofmann rearrangement Explained: The Hofmann rearrangement is a special halogenation reaction…

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Hofmann Elimination

Hofmann Elimination Hofmann Elimination Definition: Tetra-alkyl ammonium salts undergo elimination to form the least substituted alkene. This is called the Hofmann elimination. Hofmann Elimination Explained: Amines, like alcohols, contain a poor leaving group which must be converted…

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Heck Reaction

Heck Reaction Heck Reaction Definition: The Heck reaction is a coupling reaction of a vinyl or aryl halide with an alkene in the presence of a palladium catalyst which forms a more highly substituted alkene with a new carbon-carbon bond. Heck reaction Explained: The Heck reaction is the…

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Haloform reaction

Haloform reaction Haloform reaction Definition: Addition of a dihalogen (such as iodine, bromine, or chlorine) to a methyl ketone in the presence of base results in a carboxylic acid and a haloform (iodoform, bromoform, or chloroform). Haloform reaction Explained: Haloform reaction is…

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