Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
12 Cards in this Set
- Front
- Back
|
Front (Term) NaBH4 |
Weaker reductant for aldehydes ketones and acyl chlorides will not work for esters amdides or carboxylic acids |
|
|
PCl3 or SOCl2 |
Replaces alcohol with Cl |
|
|
H2SO4 |
With heat- alcohol reduced to double bond |
|
|
PCC |
Weaker oxident takes alcohol to Aldehyde or ketone |
|
|
LiAlH4 |
Pretty much reduces everything |
|
|
H2, lindlars |
Alkyne to Allene |
|
|
Pd/C, H2 |
Alkene to alkane |
|
|
H2 , Rainey nickel |
Reduces CN |
|
|
N2 / liq NH3 |
Tans alkene from alkyne C triple bond C |
|
|
DIBALH, -78c / H2O |
Ester to aldehyde (possibly alcohol) |
|
|
LiAl(tri-tert la la la)H, -78c 2. H2O |
Bulky so can only react on end -> acyl chloride to aldehyde |
|
|
BH3 |
Alkene reduction |
