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Aledyhyde/Ketone —> α-halo aldehyde/ketone
Acid-Catalysed α-halogenation

Aldehyde/Ketone —> α,α dihalo aldehyde/ketone
Base-promoted α-halogenation

Aldehyde/Ketone —> Carboxylic Acid + Haloform
HVZ Reaction

Carboxylic Acid —> α-bromo acid halide

2 Aldehydes/Ketones —> β-hydroxyaldehyde/ketone
Adol Reaction

β hydroxy aldehyde —> α,β unsaturated aldehyde
Adol Condensation

2 diff ketones/aldehydes —> β-hydroxy ketone/aldehyde mixture of products
Crossed Adol Addition
Aldehydes more reactive electrophilic bc less sterically hindered + less e- donating
ketone typically enolate donor

Ketone/Aldehyde w/ α hydrogens + w/ out—> α,β unsaturated ketone/aldehyde
Claisen-Schmidt Condensation

secondary amine —> LDA

Ketone —> enolate (2 conditions)

Ketone —> β-hydroxyketone +Cs (2 conditions)

cmpd w 2+ aldehyde/ketone —> 5/6-membered ring

2 esters —> β-keto ester
Claisen Condensation

diester —> cyclic β-keto ester
Dieckmann Condensation

ester enolates/dimethyl carbonate w/ α hydrogens + w/ out—> β-keto esters/β-diesters
Crossed Claisen Condensation

ketone + ester —> β-diketone
