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Organic Chemistry: Mechanisms, Reactivity, and Key Concepts Study Guide
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업로드한 자료에 맞춘 엄선된 수업 – 모든 주제를 단계별로 배워보세요.
Introduction to Substitution
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05:55
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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The SN2 Mechanism
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Ranking reactivity toward SN2
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08:33
Drawing the SN2 Mechanism
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11:57
Understanding the properties of SN2.
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The SN1 Mechanism
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10:49
Drawing the SN1 Mechanism
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01:13
Why highly substituted leaving groups favor SN1.
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08:16
Understanding the properties of SN1.
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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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01:49
Nucleophile or Electrophile
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02:48
How to tell if uncharged molecules will react as nucleophiles or electrophiles.
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Acid and Base Definitions
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Lewis vs. Bronsted-Lowry Definition
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00:54
The Bronsted-Lowry definition of acids and bases.
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02:11
Equilibrium constant and conjugates.
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Electronegativity
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Differences between ionic, polar and covalent bonds
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Solvents
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The difference between protic vs. aprotic solvents.
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01:16
Identification of polarity in solvents
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00:39
Identification of polarity in solvents
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Factors Affecting Acidity
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Which of the oxides is the most basic?
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03:09
The 3 factors that determine the strength of inductive effects.
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01:54
Using Inductive Effect to determine acidity
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