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Organic Chemistry: Reaction Mechanisms, Stereochemistry, and Synthesis Practice (Exam 4 Key)
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The SN2 Mechanism
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Ranking reactivity toward SN2
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Drawing the SN2 Mechanism
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11:57
Understanding the properties of SN2.
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Introduction to Substitution
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Predict the product
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05:01
Nucleophiles and Electrophiles can react in Bronsted-Lowry Reactions.
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01:47
Nucleophiles and Electrophiles can react in Substitution Reactions.
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Leaving Groups
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Predict the best leaving group
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01:12
Predict the best leaving group
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00:36
Predict the best leaving group
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Carbocation Intermediates – Stability
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Determining Carbocation Stability
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01:21
Predicting the most stable carbocation
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Reaction Mechanism
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How to tell if charged molecules will react as nucleophiles or electrophiles.
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Nucleophile or Electrophile
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How to tell if uncharged molecules will react as nucleophiles or electrophiles.
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Alkyne Hydration
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Alkyne Hydration
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Hydroboration-Oxidation
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General properties of hydroboration-oxidation.
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06:14
Acid-catalyzed hydroboration-oxidation mechanism
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Markovnikov's Rule
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Provide the mechanism
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03:38
How to add to asymmetrical double bonds.
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Cahn-Ingold-Prelog Nomenclature
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R and S Naming- Step 4
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Why stereoisomers need their own naming system.
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Determining Priorities
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Conformations
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Understanding what a conformer is.
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