Derivatives of carboxylic acid

Some of the derivatives of carboxylic acid are acid halide, acid amide, ester, acid anhydride.

A. Acid halides (R-COCl):

Nomenclature (IUPAC name- Alkanoyl chloride):

nomenclature of acid halides

Preparation:
  1. From carboxylic acid: Carboxylic acid reacts with PCl3, PCl5 or SOCl2 to give acid chloride.
preparation of acid chloride from carboxylic acid

Physical Properties:
  1. Lower members are colorless liquids having irritating odour and higher members are colorless solid.
  2. Acid chlorides are insoluble in water due to a lack of intermolecular hydrogen bonding with water.
  3. The boiling point of acid chloride is less than parent acid due to the absence of hydrogen bonding. Formyl chloride (HCOCl) is unstable.

Chemical Properties:
  1. Action with air:
action of air with ethanoyl chloride

  1. Action with ammonia
action of ammonia with acid chloride

  1. Action with alcohol:
action of alcohol with acid chloride

  1. Rosenmund reaction:
rosennmund reaction

  1. Reduction to alcohol:
reduction of acid chloride to alcohol

  1. Action with Grignard’s reagent:
grignard reagent action with ethanoyl chloride

B. Acid Amide (R-CONH2):

Nomenclature (IUPAC name- Alkanamide):
nomenclature of acid amide

Preparation:
  1. From carboxylic acid:
preparation of acid amide from carboxylic acid

  1. From partial hydrolysis of alkanenitrile:

Physical Properties:
  1. Almost all amides are colorless, odourless, and crystalline solid. Formamide is a liquid.
  2. Lower members are soluble in water due to hydrogen bond formation.
  3. They have a higher boiling point than corresponding acids.

Chemical Properties:
  1. Amphoteric Nature:
amphoteric nature of acid amide

  1. Hydrolysis:
hydrolysis of acid amide

  1. Reduction:
reduction of acid amide

  1. Dehydration:
dehydration of acid amide

  1. Action with nitrous acid:
nitrous acid reaction with acid amide

  1. Hoffman Hypobromide reaction (decarbonylation):
decarbonylation of acid amide

C. Ester (RCOOR):

Nomenclature (IUPAC name- Alkyl alkanoate):
nomenclature of ester

Preparation:
  1. From carboxylic acid (Esterification):
esterification reaction

  1. From haloalkane:
ester preparation from haloalkane

Physical Properties:
  1. Esters are colorless oily liquids with a fruity odour.
  2. They are sparingly soluble in water.
  3. The boiling points of esters are always less than corresponding carboxylic acids.

Chemical Properties:
  1. Hydrolysis:
hydrolysis of ester

  1. Reduction:
reduction of ester

  1. Ammonolysis:
ammonolysis of ester

  1. Action with PCl5:
action of PCl5 with ester

  1. Claisen condensation: Esters having -hydrogen reacts with a base like sodium ethoxide to form ethyl acetoacetate (EAA).
claisen condensation of ester

  1. Action with Grignard’s reagent:
ester reaction with grignard reagent

D. Acid anhydride:

Nomenclature (IUPAC name- Alkanoic anhydride):
iupac name of acid anhydride
Preparation:
  1. From carboxylic acid:
acid anhydride from carboxylic acid

Physical Properties:
  1. Lower members are colorless liquid having a sharp irritating smell. Higher members are colorless solids.
  2. Lower members are soluble in water.
  3. They have a higher boiling point than parent carboxylic acid.

Chemical Properties:
  1. Hydrolysis:
hydrolysis of acetic anhydride
  1. Ammonolysis:
ammonolysis of acetic anhydride
  1. Alcoholysis:
alcoholysis of acetic anhydride
  1. Reduction:
reduction of acetic anhydride
  1. Action with PCl5
action of PCl5 with acetic anhydride

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