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Organic Chemistry: Reaction Mechanisms, Stereochemistry, and Synthesis Practice (Exam 4 Key)

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SN2 Reaction

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

Nucleophilic 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

Good Leaving Groups

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

Carbocation Stability

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

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

Alkyne Hydration

  • Alkyne Hydration
    09:11

Hydroboration

  • General properties of hydroboration-oxidation.
    06:38
  • Acid-catalyzed hydroboration-oxidation mechanism
    06:14

Markovnikov

  • Provide the mechanism
    01:26
  • How to add to asymmetrical double bonds.
    03:38

R and S Configuration

  • R and S Naming- Step 4
    03:07
  • Why stereoisomers need their own naming system.
    01:48
  • Determining Priorities
    01:19

Conformational Isomers

  • Understanding what a conformer is.
    03:29