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Carboxylic Acids and Their Derivatives: Structure, Nomenclature, Properties, and Reactions

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COOH Derivatives and Nucleophilic Acyl Substitution

  • Intro to Nucleophilic Acyl Substituion
    04:06
  • Intro to Carboxylic Acid Derivatives
    03:50

Carboxylic Acid Nomenclature

  • Give the IUPAC name
    02:03
  • Carboxylic Acids Nomenclature
    04:20

Diacid Nomenclature

  • Nomenclature of Diacids
    01:22

Ester Nomenclature

  • Draw the molecule
    01:28
  • Name the structure
    01:10
  • Ester Nomenclature
    02:39

Acid Chloride Nomenclature

  • Acid Chloride Nomenclature
    03:13
  • Provide the IUPAC name for the molecule
    01:44
  • Draw the Acid-Chloride
    00:37

Anhydride Nomenclature

  • Draw the molecule
    00:40
  • Anhydride Nomenclature
    03:35
  • Provide the IUPAC name for the molecule
    02:47

Amide Nomenclature

  • Amide Nomenclature
    01:33
  • Name the molecule
    02:46
  • Draw the amide
    01:28

Nucleophilic Acyl Substitution – The Three Rules

  • NAS - The Three Rules
    09:32

Fischer Esterification – Mechanism

  • General Mechanism
    04:08
  • General Reaction
    01:08

Acid-Catalyzed Ester Hydrolysis – Mechanism

  • General Mechanism
    02:38
  • General Reaction
    01:31

Base-Catalyzed Ester Hydrolysis – Mechanism

  • Mechanism
    03:27

Lactones, Lactams and Cyclization Reactions

  • Lactones and Lactams
    05:19
  • Cyclic Anhydrides and Imides
    03:35
  • Cyclization Reaction
    01:33

Carbonation of Grignard Reagents

  • Carbonation of Grignard Reagents
    02:12

Decarboxylation

  • Predict the correct structure
    02:32
  • General Mechanism
    04:32