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Reactions and Nomenclature of Carboxylic Acids and Carboxylic Acid Derivatives

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Carboxylic Acid Derivatives

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

Naming Carboxylic Acids

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

Acid Chloride Nomenclature

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

Naming Esters

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

Naming Amides

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

Naming Nitriles

  • Name the structure
    00:50
  • Nitrile Nomenclature
    01:01
  • Draw the molecule
    00:28

Naming Anhydrides

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

Diacid Nomenclature

  • Nomenclature of Diacids
    01:22

Resonance Structures

  • How to draw a resonance hybrid.
    03:24
  • The rules you need for resonance:
    03:34
  • How to determine which structure is most stable.
    01:32

Intermolecular Forces

  • How dipole-dipole forces work.
    01:46
  • How IMFs are related to melting and boiling points.
    03:08
  • How Van der Waals forces work.
    03:01

Electrophilic Aromatic Substitution

  • EAS General Mechanism
    06:52
  • EAS Review
    03:07

Nucleophilic Substitution

  • Predict the product
    05:55
  • Nucleophiles and Electrophiles can react in Bronsted-Lowry Reactions.
    05:01
  • Nucleophiles and Electrophiles can react in Substitution Reactions.
    01:47