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14.1: Carboxylic Acid Derivatives: Overview 01:15 min
14.1: Carboxylic Acid Derivatives: Overview
14.4: Structures of Carboxylic Acid Derivatives 01:28 min
14.4: Structures of Carboxylic Acid Derivatives
14.6: Acidity and Basicity of Carboxylic Acid Derivatives 01:25 min
14.6: Acidity and Basicity of Carboxylic Acid Derivatives
14.7: Spectroscopy of Carboxylic Acid Derivatives 01:26 min
14.7: Spectroscopy of Carboxylic Acid Derivatives
14.8: Relative Reactivity of Carboxylic Acid Derivatives 01:13 min
14.8: Relative Reactivity of Carboxylic Acid Derivatives
14.17: Reactions of Acid Anhydrides 01:19 min
14.17: Reactions of Acid Anhydrides
14.22: Preparation of Amides 01:29 min
14.22: Preparation of Amides
14.23: Amides to Carboxylic Acids: Hydrolysis 01:28 min
14.23: Amides to Carboxylic Acids: Hydrolysis
14.25: Preparation of Nitriles 01:12 min
14.25: Preparation of Nitriles
15.1: Reactivity of Enols 01:18 min
15.1: Reactivity of Enols
15.2: Reactivity of Enolate Ions 01:23 min
15.2: Reactivity of Enolate Ions
15.5: Regioselective Formation of Enolates 01:33 min
15.5: Regioselective Formation of Enolates
15.8: Base-Promoted α-Halogenation of Aldehydes and Ketones 00:51 min
15.8: Base-Promoted α-Halogenation of Aldehydes and Ketones
15.11: α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction 01:15 min
15.11: α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
15.22: Crossed Aldol Reaction Using Weak Bases 01:14 min
15.22: Crossed Aldol Reaction Using Weak Bases
15.24: Crossed Aldol Reaction Using Strong Bases: Directed Aldol Reaction 00:56 min
15.24: Crossed Aldol Reaction Using Strong Bases: Directed Aldol Reaction
15.27: Esters to β-Ketoesters: Claisen Condensation Overview 01:24 min
15.27: Esters to β-Ketoesters: Claisen Condensation Overview
15.30: Intramolecular Claisen Condensation of Dicarboxylic Esters: Dieckmann Cyclization 01:13 min
15.30: Intramolecular Claisen Condensation of Dicarboxylic Esters: Dieckmann Cyclization
15.38: Conjugate Addition of Enolates: Michael Addition 01:08 min
15.38: Conjugate Addition of Enolates: Michael Addition
16.8: Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control 01:23 min
16.8: Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control
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