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Organic Chemistry
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Organic Chemistry: Basicity, Elimination, Reaction Mechanisms, and Synthesis
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Acid and Base Definitions
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07:46
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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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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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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E2 Mechanism
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04:42
Understanding the properties of E2.
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09:36
Drawing the E2 Mechanism.
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02:03
Rank reactivity toward E2
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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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Energy Diagram
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Favorability and rate of Free Energy Diagrams
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00:34
Favorability and rate of Free Energy Diagrams
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02:18
Favorability and rate of Free Energy Diagrams
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Cahn-Ingold-Prelog Nomenclature
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R and S Naming- Step 4
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01:48
Why stereoisomers need their own naming system.
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01:19
Determining Priorities
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Types of Stereoisomers
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Determine total number of stereoisomers
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01:03
How to predict the total number of stereoisomers.
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07:41
Draw stereoisomers and determine relationship
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Optical Activity
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Specific rotation vs. observed rotation.
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