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Allylic and Benzylic Reactivity: Carbocations, Radicals, Anions, and SN2 Reactions

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Allylic Halogenation

  • Specific Reactions - Allylic Chlorination
    03:
  • Allylic Halogentation - General Mechanism
    07:50
  • Specific Reactions - Allylic Bromination
    03:20

Reactions at the Allylic Position

  • 가이드 코스
    Reactions at the Allylic Position Example 1
    2:01
  • 가이드 코스
    Reactions at the Allylic Position Concept 4
    3:07
  • 가이드 코스
    Reactions at the Allylic Position Concept 1
    1:26

Allylic Halogenation

  • Predict the product(s) of the following reaction.
    04:28
  • Mechanism of Allylic Bromination.
    00:54
  • The products of Allylic Chlorination.
    00:48

Carbocation Intermediates – Stability

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

Carbocation Intermediates – Stability

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

Radical Stability

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

Radical Stability

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

Enolates

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

Introduction to 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

The SN2 Mechanism

  • Ranking reactivity toward SN2
    04:03
  • Drawing the SN2 Mechanism
    08:33
  • Understanding the properties of SN2.
    11:57