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18 Cards in this Set

  • Front
  • Back

NaNO2, HCl, H2O

+N=O

1. KMnO4, NaOH, heat


2. H+, H2O

Turns any benzylic carbons into carboxylic acids

R-CN to R-C=O

1. DIBAL-H


2. H+, H2O

eliminating an amine

1. CH3I


2. Ag2O


3. heat

make a phenol

chlorobenzene, H2O, Na2CO3, 100 C

NH2 on benzene to Cl on benzene

1. HCl, NaNO2, 0 C


2. CuCl, 60 C

carbonyl to amine

NaBH3CN, EtOH, plus half-desired amine

beta keto amine

Carbonyl, formaldehyde, amine, HCl, ethanol, heat

put on thiol protecting group

ZnCl2

take off thiol protecting group

HgCl2, CaCO3, CH3CN, H2O

NaNH2, -78 C plus benzene with good leaving group

takes an alpha hydrogen, pushes off leaving group, makes benzyne

Amide, Br2, NaOH, H2O

Hofmann rearrangement to get CO2 and primary amine

Amine plus carbonyl with NaBH3CN, EtOH

nitrogen replaces oxygen, but with single bond instead of double bond

Halogen to amine

1. NaN3


2. (1. LiAlH4 2. HCl, H2O)

NH2 on benzene to Br

1. HBr, NaNO2, 0 C


2. CuBr, 100 C

alpha keto alcohol

2 aldehydes plus thiazonium salt, NaOH, H2O

NO2 on benzene to NH2

Fe, HCl

1. DIBAL-H


2. H2O

Reduces carboxylic acid derivatives to aldehydes