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Formation of carboxylic acids
primary alcohols H2Cr2O4
Permanganate oxidation KMnO4
ozonolysis from terminal alkyne 1) O3 2) H2O
alkane side chains K2Cr2O7 and H2SO4
Grignard then 1) CO2 2) H3O+
hydrolysis of nitrile
Fischer Esterification
creating an ester from a carboxylic acid and primary alcohol
synthesis of acid chlorides
carboxylic acid and thionyl chloride (SOCl2)
reduction of carboxylic acids
BH3*THF- converts to alcohol
DIBAL-H- converts to aldehyde
LiAl(OtBu)3H- converts to aldehyde