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Alkynes: Naming, Properties, and Reactions – Comprehensive Study Notes

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Alkyne Hydration

  • Vinyl alcohols yield tautomers.
    03:51
  • Markovnikov addition of alcohols yields ketones.
    03:29

Hydrogenation of Alkynes

  • Using Dissolving Metal Reduction or Lindlar’s Catalyst to turn alkynes to alkenes.
    06:08
  • Using Catalytic hydrogenation or Wilkinson’s Catalyst to turn alkynes to alkanes.
    03:46
  • The definition of hydrogenation.
    00:48

Alkyne Hydrohalogenation

  • Double hydrohalogenation of alkynes.
    02:20
  • General properties of double addition reactions to alkynes.
    01:01

Alkyne Halogenation

  • Double halogenation of alkynes.
    02:15

Alkyne Oxidative Cleavage

  • General features of alkyne cleavage.
    02:13
  • Predict the product of the following reaction.
    03:50

Ozonolysis

  • Weak Oxidative Cleavage
    06:30

Overview of Chemical Reactions

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

Addition Reaction

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