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BH3, H2O2
converts alkyne to aldehyde
O3, DMS
converts alkene to aldehyde
AgSO4, H2SO4, H2O
converts alkyne to ketone
SOCl2
converts carboxylic acid to acid chloride
CH3OH, pyridine
converts acid chlories to esters
CH3OH, H2SO4
converts -OH to -OCH
NH3
converts acid chloride to -NH2 group
converts nu L.G. to NH
PCC
converts tertiary alcohol to aldehyde
DIBAL-H, H2O
converts ester to aldehyde
converts H-CN to aldehyde
LiAlH(CO(CO3)3)3, H2O
converts acid chloride to aldehyde
NaCr2O7
converts secondary alcohol to ketone
R2CuLi, H2O
converts acid chloride to ketone
AlCl3
converts benzene and acid chloride to ketone
HgSO4, H2SO4, H2O
converts alkyne to ketone
O3
converts alkene to ketone and aldehyde
O3, H2O
converts alkyne to 2 carboxylic acids
LiAlH4, H2O
converts carbonyl to secondary alcohol
converts R-CN to R-NH2
CH3MgBr, H2O
converts carbonyl to tertiary alcohol
converts R-CN to ketone
NaCN, HCl
converts carbonyl to CN
Ph3P-Cr2
converts carbonyl to alkene
RNH2, mild acid
converts O carbonyl to N-R
R2NH, mild acid
converts O carbonyl to NR2
CrO3, H2SO4, H2O
converts primary alcohol to carboxylic acid
converts aldehyde to carboxylic acid
CO2, H3O+
converts CH3Mg-X to carboxylic acid
KMnO4
converts two R groups to carboxylic acid
H3O+, H2O
converts R-CN to carboxylic acid
H-OR
converts Nu to OR