Name Organic Reactions
Haloform
Reaction
|
Methyl ketones, are cleaved into a carboxylate anion and a
trihalomethane by the Haloform reaction.
mechanism |
Hantzsch Pyridine Synthesis
|
A condensation reaction of two equivalents of a
β-ketoester with an aldehyde
and ammonia leads to a
1,4-dihydropyridine
mechanism |
Heck Reaction
|
The palladium-catalyzed carbon–carbon bond coupling of an alkyl, aryl or
vinyl group to an alkene
mechanism |
Hell–Volhard–Zelinskii Reaction
|
The α-hydrogen of a carboxylic acid
can be replaced by bromine or chlorine to give an
α-bromo or
α-chlorocarboxylic acid
mechanism |
Hofmann Elimination Reaction
|
The amine, is first treated with excess methyl iodide, to generate the
quaternary ammonium iodide. Subsequent treatment with silver oxide in
water gives the corresponding ammonium hydroxide
mechanism |
Hunsdiecker Reaction
|
Silver carboxylates can be decarboxylated by treatment with bromine, to
yield alkyl bromides
mechanism |
Hydroboration
|
Borane adds to carbon–carbon double bonds. The alkylboranes
obtained by the hydroboration reaction by treatment with hydroperoxide
in alkaline solution gives the corresponding alcohols.
mechanism |
[A]
[B] [C] [D] [E] [F] [G] [H] [I] [J] [K] [L]
[M] [N] [O] [P] [Q] [R] [S] [T] [U] [V] [W] [X] [Y] [Z]
|