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Lecture 29: Ch. 8. E1 Reactions. Comparison of SN1, SN2, E1, and E2 Reactions
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Lecture 28: Ch. 8. Regiochemical and Stereochemical Course of E2 Reactions
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Lecture 27: Ch. 8. Elimination Reactions. Introduction to E2 Reactions
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Lecture 26: Ch. 7. Properties of Electrophiles, Nucleophiles, and Leaving Groups
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Lecture 25: Ch. 7. Mechanistic and Stereochemical Aspects of SN1 Reactions
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Lecture 23: Ch. 7. Introduction to Alkyl Halides and Nuceophilic Substitution
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Lecture 22: Ch. 6. Energetics of Reactions
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Lecture 21: Ch. 6. Energy Diagrams, Transition States, and Reaction Rates
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Lecture 20: Ch. 6. Introduction to Understanding Organic Reactions
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Lecture 18: Ch. 5. Meso Compounds
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Lecture 19: Ch. 5. Properties of Chiral Compounds
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Lecture 17: Ch. 5. Assigning Tetrahedral Stereogenic Centers
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Lecture 16: Ch. 5. Introduction to Stereochemistry
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Lecture 15: Ch. 4. Conformations of Cyclohexane
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Lecture 14: Ch. 4. Conformations of Butane and Cycloalkanes
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Lecture 13: Ch. 4. Nomenclature of Alkanes, Conformations of Ethane
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Lecture 12: Ch. 4. Introduction to Alkanes
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Lecture 11: Ch. 3. Carbonyl Compounds, Intermolecular Forces
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Lecture 10: Ch. 3. Hydrocarbons, Alcohols, Amines
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Lecture 9: Ch. 3. Organic Compounds and Functional Groups
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Lecture 8: Ch. 2. Lewis Acids, Lewis Bases, and Organic Reaction Mechanisms
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Lecture 7: Ch. 2. Acid Strength and Equilibria
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Lecture 6: Ch. 1. Molecular Geometry. Ch. 2. Acids and Bases
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Lecture 5: Ch. 1. Orbital Models of Structure and Bonding
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Lecture 4: Ch. 1. Resonance Structures, Skeletal Structures, Bond Length
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Lecture 3: Ch. 1. Bond Polarity, Formal Charge, Lewis Structures
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Introduction - Excerpt
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Lecture 1: Ch. 1. Syllabus and Introduction
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