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Organic Chemistry: Nucleophilic Reactions, Aromaticity, and Radical Chemistry Study Guide

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Carbocation Intermediates – Stability

  • Determining Carbocation Stability
    05:58
  • Predicting the most stable carbocation
    01:21

Markovnikov

  • Provide the mechanism
    01:26
  • How to add to asymmetrical double bonds.
    03:38

Dehydration Reaction

  • Dehydration of 1° alcohols:The E2 Mechanism
    05:20
  • An extra note of caution with 1° alcohols.
    01:06
  • General features of acid-catalyzed dehydration.
    06:01

Addition Reaction

  • Provide the mechanism
    01:15
  • Features of Addition Mechanisms.
    05:39

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

Diels-Alder Reaction

  • General Features
    09:48

Diels-Alder Retrosynthesis

  • Retrosynthesis
    01:22
  • Diels-Alder Retrosynthesis
    04:02
  • Retrosynthesis
    02:37

Oxidative Cleavage

  • General properties of strong oxidative cleavage.
    06:00

Ozonolysis

  • General properties of ozonolysis.
    06:30

Radical Reaction

  • What are Radical Initiators?
    03:49
  • Heterolytic vs. Homolytic Bond Cleavage .
    04:39

Radical Stability

  • The radical stability trend.
    03:43
  • Determine which of the following radicals is the most stable.
    03:25