Naming Amides
Amides are named from the parent carboxylic acid. The stem counts all the carbon atoms in the chain including the C=O carbon, and the ending -oic acid is replaced by -amide.
• HCONH2 is methanamide
• CH3CONH2 is ethanamide
• CH3CH2CONH2 is propanamide
For a secondary amide, the group attached to the nitrogen is named as a prefix with the locant N-, to show that it is bonded to nitrogen rather than to a carbon of the chain:
Sign in free to see the rest of this lesson, the R.E.C.I.P.E. recall steps and the quiz
BrainCake is free. Make an account in seconds and pick up where this page stops.
More in Carbon-Carbon Bond Formation
- Carbon-Carbon Bond Formation
- Nitriles from Haloalkanes
- Hydroxynitriles from Carbonyls
- Reduction of Nitriles to Amines
- Hydrolysis of Nitriles to Carboxylic Acids
- Extending Carbon Chains on Benzene
- Amides
All 8 lessons in Carbon-Carbon Bond Formation · All OCR A-level Organic Chemistry topics