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Organic Chemistry Study Guide: Alkyne Reactions, Synthesis, and Lindlar Reductions

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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 Hydration

  • Alkyne Hydration
    09:11

Alkynide Synthesis and Retrosynthesis

  • Predict the major product.
    03:25
  • Provide the reagents needed
    04:17
  • Predict the major product.
    05:09

Alkyne Halogenation

  • Double halogenation of alkynes.
    02:15

Alkyne Hydrohalogenation

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

Alkane Halogenation

  • Functionalizing Alkanes
    02:47

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

Leaving Groups

  • Predict the best leaving group
    00:50
  • Predict the best leaving group
    01:12
  • Predict the best leaving group
    00:36

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