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22 Cards in this Set

  • Front
  • Back
Aldehyde --> Carboxylic Acid
R-CHO + [O] --> R-COOH

K2Cr2O7 / H2SO4

Reflux
Aldehyde --> Primary Alcohol
R-CHO + 2[H] --> R-CH2(OH)

NaBH4
Ketone --> Secondary Alcohol
R-CO-R' +2[H] --> R-CH(OH)-R'

NaBH4
Carboxylic Acid --> Ester
R-COOH + R'-OH --> R-COO-R' + H2O

Dilute. H2SO4

Heat
Carboxylic Acid + Group 1 Metal (Sodium)
R-COOH + Na --> R-COO-Na+ + 1/2H2
Carboxylic Acid + Group 1 Metal Hydroxide (Sodium Hydroxide)
R-COOH + NaOH --> R-COO-Na+ + H2O
Carboxylic Acid + Group 1 Metal Carbonate (Sodium Carbonate)
2R-COOH + Na2CO3 --> 2R-COO-Na+ + H2O + CO2
Carboxylic Acid + Group 2 Metal (Magnesium)
2R-COOH + Mg --> (R-COO-)2Mg2+ + H2
Carboxylic Acid + Group 2 Metal Hydroxide (Magnesium)
2R-COOH + Mg(OH)2 --> (R-COO-)2Mg2+ + 2H2O
Carboxylic Acid + Group 2 Metal Carbonate
2R-COOH + MgCO3 --> (R-COO-)2Mg2+ + H2O + CO2
Acid Hydrolysis of Esters
R-COO-R' --> R-COOH + R'-OH

HCl

Room temperature, reflux
Alkaline Hydrolysis of Esters
R-COO-R' --> R-COO-Na+

NaOH

Room temperature, reflux
Benzene --> Nitrobenzene
C6H6 + HNO3 --> C6H5NO2 + H2O

conc. H2SO4

50-55 deg.cel.
Nitrobenzene --> Phenylamine
C6H5NO2 + 6[H] --> C6H5NH2 + 2H2O

Sn/ conc. HCl

Room temperature, reflux
Formation of Nitrous Acid
NaNO2 + HCl --> HNO2 + NaCl
Formation of diazonium compound after nitrous acid has been made in situ
C6H5NH2 + HNO2 + ex.HCl --> C6H5N+≡N Cl- + 2H2O

Less than 10 deg.cel.
Coupling reaction with phenol
C6H5N+≡N Cl- + C6H5OH --> C6H5-N=N-C6H4OH + HCl

Alkaline solution
Benzene --> Bromobenzene
C6H6 + Br2 --> C6H5Br + HBr

AlBr3 / FeBr3
Phenol --> 2,4,6-tribromophenol
C6H5OH + 3Br2 --> C6H2(Br)3OH + 3HBr

Room Temperature
Phenol --> Sodium Phenoxide
C6H5OH + NaOH --> C6H5O-Na+ + H2O
Phenol --> Magnesium Phenoxide
2C6H5OH + Mg --> (C6H5O-)2Mg2+ + H2
Halogenoalkane -> aliphatic amine
R-X + NH3 --> R-NH2 + HX

Ethanol as solvent

Warm gently