Apr 12, 2014
Wolff-Kishner Reaction
Removes the carbonyl functional group.
Hydrazone comes from Carbonyl rection with NH2X
seen from Canada
seen from United States
seen from United States
seen from Italy
seen from China
seen from Türkiye
seen from China
seen from Malaysia
seen from United States
seen from United States
seen from United States
seen from United States
seen from United Kingdom
seen from Russia
seen from Canada
seen from United States
seen from United States
seen from Russia
seen from Türkiye
seen from Canada
Wolff-Kishner Reaction
Removes the carbonyl functional group.
Hydrazone comes from Carbonyl rection with NH2X
Creation of an Imine from a Carbonyl
A reversible process also driven by the removal of H2O
All NH2X react like this
Acetal Formation, driven by the removal of H2O
the entire process is reversible. It is a great way to protect ketones/aldehydes (carbonyls) from being attacked
It favors the Aldehyde. (Most likely due to steric reasons)
Acetal Formation
S Ylide Reaction
Sulfur is oxyphilic, but not as much as P
Wittig Reaction
Notes: Phenyl shorthand is what my Prof uses, not official
Phosphorus is very oxyphilic