Amides (OCR A Level Chemistry A): Revision Note

Exam code: H432

Stewart Hird

Written by: Stewart Hird

Reviewed by: Caroline Carroll

Updated on

Amides

  • Amides are formed from the condensation reaction of carboxylic acids or acyl chlorides with ammonia or amines

  • Amides are common in nature such as in proteins where the amine and carboxylic acid groups of amino acids bond together

  • Amides have a general structure of RCONR2

6-4-4-general-structure-of-an-amide

The general structure of an amide

  • Amides can be classified as primary, secondary or tertiary amides

  • Like amines, this is done as a comparison to ammonia, depending on the number of substitutions on the amide nitrogen 

    • Primary amide - one carbon bonded to the amide nitrogen 

      • R' and R'' are both hydrogen atoms so one "ammonia" hydrogen has been substituted with the carbonyl group from the RCO portion of the molecule

    • Secondary amide - two carbons bonded to the amide nitrogen (one MUST be the carbonyl carbon)

    • Tertiary amide - three carbons bonded to the amide nitrogen (one MUST be the carbonyl carbon)

Naming primary amides

  • For primary amides, we simply add -amide to the stem name

    • e.g. CH3CONH2

      • Contains two carbons with a C-C (ethan-) and an amide group (-amide)

      • This gives us ethanamide

Naming secondary amides

  • For secondary amides, the alkyl chain attached to the nitrogen is added at the start of the chemical name

  • This alkyl chain is prefixed with N-

  • The chain containing the carbonyl group is named the same as a primary amide

    • e.g. CH3CONH(C3H7)

      • Contains a propyl group on the nitrogen (N-propyl) 

      • Contains two carbons with a C-C (ethan-) and an amide group (-amide)

      • This gives us N-propylethanamide

Naming tertiary amides

  • For tertiary amides, there are two alkyl chains attached to the nitrogen

  • The naming of these chains is the same as secondary amides

  • As with standard nomenclature, these chains are listed in alphabetical order and the prefix 'di-' is used if necessary

    • e.g. CH3CONCH3(C3H7)

      • Contains a methyl group on the nitrogen (N-methyl)

      • Contains a propyl group on the nitrogen (N-propyl) 

      • Contains two carbons with a C-C (ethan-) and an amide group (-amide)

      • This gives us N-methyl-N-propylethanamide

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Stewart Hird

Author: Stewart Hird

Expertise: Chemistry Content Creator

Stewart has been an enthusiastic GCSE, IGCSE, A Level and IB teacher for more than 30 years in the UK as well as overseas, and has also been an examiner for IB and A Level. As a long-standing Head of Science, Stewart brings a wealth of experience to creating Topic Questions and revision materials for Save My Exams. Stewart specialises in Chemistry, but has also taught Physics and Environmental Systems and Societies.

Caroline Carroll

Reviewer: Caroline Carroll

Expertise: Head of Content Delivery

Caroline graduated from the University of Nottingham with a degree in Chemistry and Molecular Physics. She spent several years working as an Industrial Chemist in the automotive industry before retraining to teach. Caroline has over 12 years of experience teaching GCSE and A-level chemistry and physics. She is passionate about delivering high-quality resources to help students achieve their full potential.