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Alkenes and Alkynes: Nomenclature, Stability, and Reactions

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Naming Alkenes

  • Name the following alkene
    02:04
  • How to name alkenes and alkynes
    01:55

Cis vs Trans

  • Why we need to use the E/Z naming system
    02:07
  • What does E and Z stand for?
    00:50
  • How to name different types of double bonds or rings
    04:28

E2 Mechanism

  • Understanding the properties of E2.
    04:42
  • Drawing the E2 Mechanism.
    09:36
  • Rank reactivity toward E2
    02:03

Zaitsev Rule

  • Hofmann product
    02:39
  • Defining Zaitsev’s Rule
    01:18
  • Zaitsev product
    07:01

Dehydrohalogenation

  • The dehydrohalogenation mechanism.
    03:02
  • Dehydrohalogenation mechanism and products
    04:35

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

Alkyne Hydration

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

Hydrogenation

  • General properties of catalytic hydrogenation.
    05:21

Ozonolysis

  • General properties of ozonolysis.
    06:30

Preparation of Organometallics

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

Alkynide Synthesis

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

Nucleophilic Addition

  • Nucleophilic Addition
    08:27

Reaction Mechanism

  • How to tell if charged molecules will react as nucleophiles or electrophiles.
    02:39
  • Nucleophile or Electrophile
    01:49
  • How to tell if uncharged molecules will react as nucleophiles or electrophiles.
    02:48