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Chapter 10: Organohalides – Structures, Nomenclature, and Reactions

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Naming Alkyl Halides

  • How to name alkyl halides
    01:52
  • Name the following alkyl halide
    01:58
  • Name the following alkyl halide
    03:53

Alkyl Groups

  • Name the following alkane
    02:33
  • Understanding Non-IUPAC Substituents
    06:42
  • Name the following alkane
    03:56

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

Free Radical Halogenation

  • The one reaction that alkanes will actually undergo.
    02:05
  • Explaining the following problem.
    00:34
  • Show the entire chain reaction mechanism.
    04:08

Radical Selectivity

  • Predict the Product.
    00:48
  • Predict the Product.
    01:02
  • Using the Hammond Postulate to describe radical chlorination.
    03:03

Radical Synthesis

  • Predict the MAJOR product.
    04:12
  • Predict the MAJOR product.
    04:28

Grignard Reaction

  • Reactions of Organometallics
    13:40

Preparation of Organometallics

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

Suzuki Reaction

  • Suzuki Reaction Example 1
    03:58
  • Suzuki Reaction
    04:02
  • Suzuki Reaction
    03:22

Overview of Chemical Reactions

  • Recognizing Substitution Reactions.
    01:34
  • Recognizing Acid-Base Reactions.
    02:43
  • Recognizing Elimination Reactions.
    00:40