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Organic Chemistry II (CHM 304) Syllabus and Course Structure – Medgar Evers College

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Aromaticity

  • Intro to Aromaticity
    08:19

Electrophilic Aromatic Substitution

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

Nucleophilic Aromatic Substitution

  • The Meisenheimer Complex
    06:23
  • Which ipso-substitution is more favored
    03:30
  • General Mechanism
    06:45

Infrared Spectroscopy

  • General Features of IR Spect
    16:04

NMR Spectroscopy

  • General NMR Features
    10:06

Mass Spectrometry

  • Equipment and Theory
    10:48
  • How to Read a Mass Spectrum
    01:25

Preparation of Organometallics

  • Ruining Organometallics
    02:50
  • General Reaction
    12:21

Alcohol Synthesis

  • Forming alcohols through SN2 reactions.
    01:44
  • Forming alcohols through Acid-Catalyzed Hydration.
    02:02
  • Forming alcohols through Hydroboration-Oxidation.
    01:37

Epoxide Reactions

  • Base-Catalyzed Epoxide Ring-Opening
    04:44
  • Acid-Catalyzed Epoxide Ring-Opening
    04:34

Ketone and Aldehyde Synthesis Reactions

    Naming Carboxylic Acids

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

    Carboxylic Acid Derivatives

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

    Enolate

    • General Reactions
      02:28
    • Formation of Enolates
      02:26