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Organic Chemistry

Video textbook for undergraduate courses: Visualized concepts and experiments

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21 Chapters

391 Videos

2,600+ Multiple Choice Questions

Table of Contents

Chapter 1

Covalent Bonding and Structure

15 Videos · 38 Minutes

Chapter 2

Thermodynamics and Chemical Kinetics

12 Videos · 28 Minutes

Chapter 3

Alkanes and Cycloalkanes

14 Videos · 32 Minutes

Chapter 4

Stereoisomerism

12 Videos · 29 Minutes

Chapter 5

Acids and Bases

7 Videos · 16 Minutes

Chapter 6

Nucleophilic Substitution and Elimination Reactions of Alkyl Halides

20 Videos · 49 Minutes

Chapter 7

Alkene Structure and Reactivity

7 Videos · 16 Minutes

Chapter 8

Reactions of Alkenes

15 Videos · 37 Minutes

Chapter 9

Alkynes

12 Videos · 30 Minutes

Chapter 10

Alcohols and Phenols

12 Videos · 28 Minutes

Chapter 11

Ethers, Epoxides, Sulfides

15 Videos · 37 Minutes

Chapter 12

Aldehydes and Ketones

25 Videos · 32 Minutes
Structures of Aldehydes and Ketones 1:04

12.1: Structures of Aldehydes and Ketones

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IUPAC Nomenclature of Aldehydes 1:16

12.2: IUPAC Nomenclature of Aldehydes

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IUPAC Nomenclature of Ketones 1:09

12.3: IUPAC Nomenclature of Ketones

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Common Names of Aldehydes and Ketones 1:11

12.4: Common Names of Aldehydes and Ketones

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IR and UV–Vis Spectroscopy of Aldehydes and Ketones 1:29

12.5: IR and UV–Vis Spectroscopy of Aldehydes and Ketones

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NMR Spectroscopy and Mass Spectrometry of Aldehydes and Ketones 1:15

12.6: NMR Spectroscopy and Mass Spectrometry of Aldehydes and Ketones

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Preparation of Aldehydes and Ketones from Alcohols, Alkenes, and Alkynes 1:33

12.7: Preparation of Aldehydes and Ketones from Alcohols, Alkenes, and Alkynes

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Preparation of Aldehydes and Ketones from Nitriles and Carboxylic Acids 1:24

12.8: Preparation of Aldehydes and Ketones from Nitriles and Carboxylic Acids

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Preparation of Aldehydes and Ketones from Carboxylic Acid Derivatives 1:18

12.9: Preparation of Aldehydes and Ketones from Carboxylic Acid Derivatives

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Nucleophilic Addition to the Carbonyl Group: General Mechanism 1:18

12.10: Nucleophilic Addition to the Carbonyl Group: General Mechanism

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Aldehydes and Ketones with Water: Hydrate Formation 1:20

12.11: Aldehydes and Ketones with Water: Hydrate Formation

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Aldehydes and Ketones with Alcohols: Hemiacetal Formation 1:19

12.12: Aldehydes and Ketones with Alcohols: Hemiacetal Formation

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Protecting Groups for Aldehydes and Ketones: Introduction 1:23

12.13: Protecting Groups for Aldehydes and Ketones: Introduction

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Acetals and Thioacetals as Protecting Groups for Aldehydes and Ketones 1:24

12.14: Acetals and Thioacetals as Protecting Groups for Aldehydes and Ketones

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Aldehydes and Ketones with HCN: Cyanohydrin Formation Overview 1:32

12.15: Aldehydes and Ketones with HCN: Cyanohydrin Formation Overview

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Aldehydes and Ketones with HCN: Cyanohydrin Formation Mechanism 1:10

12.16: Aldehydes and Ketones with HCN: Cyanohydrin Formation Mechanism

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Aldehydes and Ketones to Alkenes: Wittig Reaction Overview 1:19

12.17: Aldehydes and Ketones to Alkenes: Wittig Reaction Overview

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Aldehydes and Ketones to Alkenes: Wittig Reaction Mechanism 1:14

12.18: Aldehydes and Ketones to Alkenes: Wittig Reaction Mechanism

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Aldehydes and Ketones with Amines: Imine and Enamine Formation Overview 1:16

12.19: Aldehydes and Ketones with Amines: Imine and Enamine Formation Overview

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Aldehydes and Ketones with Amines: Imine Formation Mechanism 1:23

12.20: Aldehydes and Ketones with Amines: Imine Formation Mechanism

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Aldehydes and Ketones with Amines: Enamine Formation Mechanism 1:14

12.21: Aldehydes and Ketones with Amines: Enamine Formation Mechanism

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Aldehydes and Ketones to Alkanes: Wolff–Kishner Reduction 1:09

12.22: Aldehydes and Ketones to Alkanes: Wolff–Kishner Reduction

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Oxidations of Aldehydes and Ketones to Carboxylic Acids 1:15

12.23: Oxidations of Aldehydes and Ketones to Carboxylic Acids

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Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation 1:22

12.24: Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation

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Keto–Enol Tautomerism: Mechanism 1:14

12.25: Keto–Enol Tautomerism: Mechanism

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Chapter 13

Carboxylic Acids

17 Videos · 23 Minutes

Chapter 14

Carboxylic Acid Derivatives

28 Videos · 34 Minutes
Carboxylic Acid Derivatives: Overview 1:15

14.1: Carboxylic Acid Derivatives: Overview

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Nomenclature of Carboxylic Acid Derivatives: Acid Halides, Esters, and Acid Anhydrides 1:16

14.2: Nomenclature of Carboxylic Acid Derivatives: Acid Halides, Esters, and Acid Anhydrides

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Nomenclature of Carboxylic Acid Derivatives: Amides and Nitriles 1:11

14.3: Nomenclature of Carboxylic Acid Derivatives: Amides and Nitriles

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Structures of Carboxylic Acid Derivatives 1:28

14.4: Structures of Carboxylic Acid Derivatives

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Physical Properties of Carboxylic Acid Derivatives 1:19

14.5: Physical Properties of Carboxylic Acid Derivatives

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Acidity and Basicity of Carboxylic Acid Derivatives 1:25

14.6: Acidity and Basicity of Carboxylic Acid Derivatives

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Spectroscopy of Carboxylic Acid Derivatives 1:26

14.7: Spectroscopy of Carboxylic Acid Derivatives

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Relative Reactivity of Carboxylic Acid Derivatives 1:13

14.8: Relative Reactivity of Carboxylic Acid Derivatives

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Nucleophilic Acyl Substitution of Carboxylic Acid Derivatives 1:15

14.9: Nucleophilic Acyl Substitution of Carboxylic Acid Derivatives

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Acid Halides to Carboxylic Acids: Hydrolysis 1:01

14.10: Acid Halides to Carboxylic Acids: Hydrolysis

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Acid Halides to Esters: Alcoholysis 1:12

14.11: Acid Halides to Esters: Alcoholysis

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Acid Halides to Amides: Aminolysis 1:07

14.12: Acid Halides to Amides: Aminolysis

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Acid Halides to Alcohols: LiAlH<sub>4</sub> Reduction 1:19

14.13: Acid Halides to Alcohols: LiAlH4 Reduction

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Acid Halides to Alcohols: Grignard Reaction 1:15

14.14: Acid Halides to Alcohols: Grignard Reaction

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Acid Halides to Ketones: Gilman Reagent 1:14

14.15: Acid Halides to Ketones: Gilman Reagent

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Preparation of Acid Anhydrides 1:07

14.16: Preparation of Acid Anhydrides

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Reactions of Acid Anhydrides 1:19

14.17: Reactions of Acid Anhydrides

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Esters to Carboxylic Acids: Saponification 1:25

14.18: Esters to Carboxylic Acids: Saponification

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Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis 1:13

14.19: Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis

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Esters to Alcohols: Hydride Reductions 1:17

14.20: Esters to Alcohols: Hydride Reductions

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Esters to Alcohols: Grignard Reaction 1:08

14.21: Esters to Alcohols: Grignard Reaction

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Preparation of Amides 1:29

14.22: Preparation of Amides

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Amides to Carboxylic Acids: Hydrolysis 1:28

14.23: Amides to Carboxylic Acids: Hydrolysis

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Amides to Amines: LiAlH<sub>4</sub> Reduction 1:20

14.24: Amides to Amines: LiAlH4 Reduction

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Preparation of Nitriles 1:12

14.25: Preparation of Nitriles

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Nitriles to Carboxylic Acids: Hydrolysis 1:08

14.26: Nitriles to Carboxylic Acids: Hydrolysis

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Nitriles to Ketones: Grignard Reaction 0:57

14.27: Nitriles to Ketones: Grignard Reaction

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Nitriles to Amines: LiAlH<sub>4</sub> Reduction 0:55

14.28: Nitriles to Amines: LiAlH4 Reduction

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Chapter 15

α-Carbon Chemistry: Enols, Enolates, and Enamines

40 Videos · 49 Minutes
Reactivity of Enols 1:18

15.1: Reactivity of Enols

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Reactivity of Enolate Ions 1:23

15.2: Reactivity of Enolate Ions

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Types of Enols and Enolates 1:19

15.3: Types of Enols and Enolates

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Enolate Mechanism Conventions 1:15

15.4: Enolate Mechanism Conventions

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Regioselective Formation of Enolates 1:33

15.5: Regioselective Formation of Enolates

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Stereochemical Effects of Enolization 1:12

15.6: Stereochemical Effects of Enolization

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Acid-Catalyzed α-Halogenation of Aldehydes and Ketones 1:21

15.7: Acid-Catalyzed α-Halogenation of Aldehydes and Ketones

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Base-Promoted α-Halogenation of Aldehydes and Ketones 0:51

15.8: Base-Promoted α-Halogenation of Aldehydes and Ketones

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Multiple Halogenation of Methyl Ketones: Haloform Reaction 1:28

15.9: Multiple Halogenation of Methyl Ketones: Haloform Reaction

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α-Halogenation of Carboxylic Acid Derivatives: Overview 1:14

15.10: α-Halogenation of Carboxylic Acid Derivatives: Overview

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α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction 1:15

15.11: α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction

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Reactions of α-Halocarbonyl Compounds: Nucleophilic Substitution 1:17

15.12: Reactions of α-Halocarbonyl Compounds: Nucleophilic Substitution

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Nitrosation of Enols 1:19

15.13: Nitrosation of Enols

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C–C Bond Formation: Aldol Condensation Overview 1:10

15.14: C–C Bond Formation: Aldol Condensation Overview

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Base-Catalyzed Aldol Addition Reaction 1:08

15.15: Base-Catalyzed Aldol Addition Reaction

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Acid-Catalyzed Aldol Addition Reaction 1:15

15.16: Acid-Catalyzed Aldol Addition Reaction

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Dehydration of Aldols to Enals: Base-Catalyzed Aldol Condensation 1:14

15.17: Dehydration of Aldols to Enals: Base-Catalyzed Aldol Condensation

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Dehydration of Aldols to Enones: Acid-Catalyzed Aldol Condensation 0:43

15.18: Dehydration of Aldols to Enones: Acid-Catalyzed Aldol Condensation

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Intramolecular Aldol Reaction 1:18

15.19: Intramolecular Aldol Reaction

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C–C Bond Cleavage: Retro-Aldol Reaction 0:57

15.20: C–C Bond Cleavage: Retro-Aldol Reaction

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Crossed Aldol Reactions: Overview 1:04

15.21: Crossed Aldol Reactions: Overview

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Crossed Aldol Reaction Using Weak Bases 1:14

15.22: Crossed Aldol Reaction Using Weak Bases

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Ketones with Nonenolizable Aromatic Aldehydes: Claisen–Schmidt Condensation 1:01

15.23: Ketones with Nonenolizable Aromatic Aldehydes: Claisen–Schmidt Condensation

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Crossed Aldol Reaction Using Strong Bases: Directed Aldol Reaction 0:56

15.24: Crossed Aldol Reaction Using Strong Bases: Directed Aldol Reaction

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Aldol Condensation with β-Diesters: Knoevenagel Condensation 1:27

15.25: Aldol Condensation with β-Diesters: Knoevenagel Condensation

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Esters to β-Ketoesters: Claisen Condensation Overview 1:24

15.26: Esters to β-Ketoesters: Claisen Condensation Overview

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Esters to β-Ketoesters: Claisen Condensation Mechanism 1:08

15.27: Esters to β-Ketoesters: Claisen Condensation Mechanism

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Aldol Condensation vs Claisen Condensation 1:33

15.28: Aldol Condensation vs Claisen Condensation

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Intramolecular Claisen Condensation of Dicarboxylic Esters: Dieckmann Cyclization 1:13

15.29: Intramolecular Claisen Condensation of Dicarboxylic Esters: Dieckmann Cyclization

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β-Dicarbonyl Compounds via Crossed Claisen Condensations 1:18

15.30: β-Dicarbonyl Compounds via Crossed Claisen Condensations

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α-Alkylation of Ketones via Enolate Ions 1:10

15.31: α-Alkylation of Ketones via Enolate Ions

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Factors Affecting α-Alkylation of Ketones: Choice of Base 1:10

15.32: Factors Affecting α-Alkylation of Ketones: Choice of Base

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Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis 1:07

15.33: Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis

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Alkylation of β-Diester Enolates: Malonic Ester Synthesis 1:14

15.34: Alkylation of β-Diester Enolates: Malonic Ester Synthesis

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Conjugate Addition to α,β-Unsaturated Carbonyl Compounds 1:09

15.35: Conjugate Addition to α,β-Unsaturated Carbonyl Compounds

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Conjugate Addition (1,4-Addition) vs Direct Addition (1,2-Addition) 1:27

15.36: Conjugate Addition (1,4-Addition) vs Direct Addition (1,2-Addition)

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Conjugate Addition of Enolates: Michael Addition 1:08

15.37: Conjugate Addition of Enolates: Michael Addition

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Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation 1:27

15.38: Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation

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Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine Reaction 1:26

15.39: Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine Reaction

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Nonenolizable Aldehydes to Acids and Alcohols: The Cannizzaro Reaction 1:25

15.40: Nonenolizable Aldehydes to Acids and Alcohols: The Cannizzaro Reaction

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Chapter 16

Dienes, Conjugated Pi Systems, and Pericyclic Reactions

27 Videos · 37 Minutes
Structure of Conjugated Dienes 1:16

16.1: Structure of Conjugated Dienes

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Stability of Conjugated Dienes 1:28

16.2: Stability of Conjugated Dienes

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π Molecular Orbitals of 1,3-Butadiene 1:24

16.3: π Molecular Orbitals of 1,3-Butadiene

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π Molecular Orbitals of the Allyl Cation and Anion 1:18

16.4: π Molecular Orbitals of the Allyl Cation and Anion

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π Molecular Orbitals of the Allyl Radical 1:27

16.5: π Molecular Orbitals of the Allyl Radical

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Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene 1:17

16.6: Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene

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Electrophilic 1,2- and 1,4-Addition of X<sub>2</sub> to 1,3-Butadiene 1:14

16.7: Electrophilic 1,2- and 1,4-Addition of X2 to 1,3-Butadiene

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Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control 1:23

16.8: Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control

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UV–Vis Spectroscopy of Conjugated Systems 1:32

16.9: UV–Vis Spectroscopy of Conjugated Systems

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UV–Vis Spectroscopy: Woodward–Fieser Rules 1:29

16.10: UV–Vis Spectroscopy: Woodward–Fieser Rules

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Pericyclic Reactions: Introduction 1:17

16.11: Pericyclic Reactions: Introduction

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Thermal and Photochemical Electrocyclic Reactions: Overview 1:26

16.12: Thermal and Photochemical Electrocyclic Reactions: Overview

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Thermal Electrocyclic Reactions: Stereochemistry 1:17

16.13: Thermal Electrocyclic Reactions: Stereochemistry

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Photochemical Electrocyclic Reactions: Stereochemistry 1:26

16.14: Photochemical Electrocyclic Reactions: Stereochemistry

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Cycloaddition Reactions: Overview 1:16

16.15: Cycloaddition Reactions: Overview

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Cycloaddition Reactions: MO Requirements for Thermal Activation 1:16

16.16: Cycloaddition Reactions: MO Requirements for Thermal Activation

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Cycloaddition Reactions: MO Requirements for Photochemical Activation 1:12

16.17: Cycloaddition Reactions: MO Requirements for Photochemical Activation

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[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction 1:16

16.18: [4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

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Diels–Alder vs Retro-Diels–Alder Reaction: Thermodynamic Factors 1:31

16.19: Diels–Alder vs Retro-Diels–Alder Reaction: Thermodynamic Factors

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Diels–Alder Reaction Forming Cyclic Products: Stereochemistry 1:28

16.20: Diels–Alder Reaction Forming Cyclic Products: Stereochemistry

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Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry 1:29

16.21: Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry

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Diels–Alder Reaction: Characteristics of Dienes 1:29

16.22: Diels–Alder Reaction: Characteristics of Dienes

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Diels–Alder Reaction: Characteristics of Dienophiles 1:24

16.23: Diels–Alder Reaction: Characteristics of Dienophiles

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Thermal Sigmatropic Reactions: Overview 1:16

16.24: Thermal Sigmatropic Reactions: Overview

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[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement 1:21

16.25: [3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement

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[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement 1:24

16.26: [3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement

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Woodward–Hoffmann Selection Rules and Microscopic Reversibility 1:34

16.27: Woodward–Hoffmann Selection Rules and Microscopic Reversibility

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Chapter 17

Aromatic Compounds

12 Videos · 15 Minutes

Chapter 18

Reactions of Aromatic Compounds

25 Videos · 32 Minutes
NMR Spectroscopy of Benzene Derivatives 1:34

18.1: NMR Spectroscopy of Benzene Derivatives

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Reactions at the Benzylic Position: Oxidation and Reduction 0:59

18.2: Reactions at the Benzylic Position: Oxidation and Reduction

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Reactions at the Benzylic Position: Halogenation 1:11

18.3: Reactions at the Benzylic Position: Halogenation

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Electrophilic Aromatic Substitution: Overview 1:16

18.4: Electrophilic Aromatic Substitution: Overview

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Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene 1:15

18.5: Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene

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Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene 1:13

18.6: Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene

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Electrophilic Aromatic Substitution: Nitration of Benzene 1:20

18.7: Electrophilic Aromatic Substitution: Nitration of Benzene

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Electrophilic Aromatic Substitution: Sulfonation of Benzene 1:22

18.8: Electrophilic Aromatic Substitution: Sulfonation of Benzene

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Electrophilic Aromatic Substitution: Friedel–Crafts Alkylation of Benzene 1:17

18.9: Electrophilic Aromatic Substitution: Friedel–Crafts Alkylation of Benzene

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Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene 1:11

18.10: Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene

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Limitations of Friedel–Crafts Reactions 1:26

18.11: Limitations of Friedel–Crafts Reactions

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Directing Effect of Substituents: <em>ortho</em>–<em>para</em>-Directing Groups 1:14

18.12: Directing Effect of Substituents: orthopara-Directing Groups

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Directing Effect of Substituents: <em>meta</em>-Directing Groups 1:09

18.13: Directing Effect of Substituents: meta-Directing Groups

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<em>ortho</em>–<em>para</em>-Directing Activators: –CH<sub>3</sub>, –OH, –&NoBreak;NH<sub>2</sub>, –OCH<sub>3</sub> 1:11

18.14: orthopara-Directing Activators: –CH3, –OH, –⁠NH2, –OCH3

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<em>ortho</em>–<em>para</em>-Directing Deactivators: Halogens 1:24

18.15: orthopara-Directing Deactivators: Halogens

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<em>meta</em>-Directing Deactivators: –NO<sub>2</sub>, –CN, –CHO, –&NoBreak;CO<sub>2</sub>R, –COR, –CO<sub>2</sub>H 1:13

18.16: meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H

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Directing and Steric Effects in Disubstituted Benzene Derivatives 1:18

18.17: Directing and Steric Effects in Disubstituted Benzene Derivatives

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Nucleophilic Aromatic Substitution: Addition–Elimination (S<sub>N</sub>Ar) 1:30

18.18: Nucleophilic Aromatic Substitution: Addition–Elimination (SNAr)

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Nucleophilic Aromatic Substitution: Elimination–Addition 1:11

18.19: Nucleophilic Aromatic Substitution: Elimination–Addition

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Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic S<sub>N</sub>1 1:14

18.20: Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic SN1

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Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation 1:28

18.21: Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation

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Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism 1:18

18.22: Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism

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Hydrolysis of Chlorobenzene to Phenol: Dow Process 1:10

18.23: Hydrolysis of Chlorobenzene to Phenol: Dow Process

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Benzene to Phenol via Cumene: Hock Process 1:27

18.24: Benzene to Phenol via Cumene: Hock Process

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Oxidation of Phenols to Quinones 1:17

18.25: Oxidation of Phenols to Quinones

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Chapter 19

Amines

29 Videos · 38 Minutes
Amines: Introduction 1:07

19.1: Amines: Introduction

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Nomenclature of Primary Amines 1:17

19.2: Nomenclature of Primary Amines

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Nomenclature of Secondary and Tertiary Amines 1:12

19.3: Nomenclature of Secondary and Tertiary Amines

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Nomenclature of Aryl and Heterocyclic Amines 1:10

19.4: Nomenclature of Aryl and Heterocyclic Amines

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Structure of Amines 1:19

19.5: Structure of Amines

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Physical Properties of Amines 1:26

19.6: Physical Properties of Amines

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Basicity of Aliphatic Amines 1:21

19.7: Basicity of Aliphatic Amines

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Basicity of Aromatic Amines 1:18

19.8: Basicity of Aromatic Amines

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Basicity of Heterocyclic Aromatic Amines 1:25

19.9: Basicity of Heterocyclic Aromatic Amines

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NMR Spectroscopy Of Amines 1:19

19.10: NMR Spectroscopy Of Amines

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Mass Spectrometry of Amines 1:15

19.11: Mass Spectrometry of Amines

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Preparation of Amines: Alkylation of Ammonia and Amines 1:30

19.12: Preparation of Amines: Alkylation of Ammonia and Amines

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Preparation of 1° Amines: Azide Synthesis 1:22

19.13: Preparation of 1° Amines: Azide Synthesis

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Preparation of 1° Amines: Gabriel Synthesis 1:28

19.14: Preparation of 1° Amines: Gabriel Synthesis

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Preparation of Amines: Reduction of Oximes and Nitro Compounds 1:29

19.15: Preparation of Amines: Reduction of Oximes and Nitro Compounds

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Preparation of Amines: Reduction of Amides and Nitriles 1:13

19.16: Preparation of Amines: Reduction of Amides and Nitriles

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Preparation of Amines: Reductive Amination of Aldehydes and Ketones 1:38

19.17: Preparation of Amines: Reductive Amination of Aldehydes and Ketones

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Preparation of 1° Amines: Hofmann and Curtius Rearrangement Overview 1:07

19.18: Preparation of 1° Amines: Hofmann and Curtius Rearrangement Overview

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Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism 1:26

19.19: Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism

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Amines to Amides: Acylation of Amines 1:19

19.20: Amines to Amides: Acylation of Amines

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Amines to Alkenes: Hofmann Elimination 1:16

19.21: Amines to Alkenes: Hofmann Elimination

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Amines to Alkenes: Cope Elimination 1:14

19.22: Amines to Alkenes: Cope Elimination

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1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO<sub>2</sub> Overview 1:26

19.23: 1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview

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1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO<sub>2</sub> Mechanism 1:37

19.24: 1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism

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2° Amines to <em>N</em>-Nitrosamines: Reaction with NaNO<sub>2</sub> 1:20

19.25: 2° Amines to N-Nitrosamines: Reaction with NaNO2

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Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions 1:20

19.26: Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions

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Diazonium Group Substitution: –OH and –H 1:19

19.27: Diazonium Group Substitution: –OH and –H

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Aryldiazonium Salts to Azo Dyes: Diazo Coupling 1:11

19.28: Aryldiazonium Salts to Azo Dyes: Diazo Coupling

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Amines to Sulfonamides: The Hinsberg Test 1:23

19.29: Amines to Sulfonamides: The Hinsberg Test

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Chapter 20

Radical Chemistry

27 Videos · 34 Minutes
Radicals: Electronic Structure and Geometry 1:07

20.1: Radicals: Electronic Structure and Geometry

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Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals 1:17

20.2: Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals

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Radical Formation: Overview 1:03

20.3: Radical Formation: Overview

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Radical Formation: Homolysis 0:54

20.4: Radical Formation: Homolysis

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Radical Formation: Abstraction 0:47

20.5: Radical Formation: Abstraction

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Radical Formation: Addition 0:47

20.6: Radical Formation: Addition

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Radical Formation: Elimination 0:51

20.7: Radical Formation: Elimination

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Radical Reactivity: Overview 1:11

20.8: Radical Reactivity: Overview

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Radical Reactivity: Steric Effects 1:10

20.9: Radical Reactivity: Steric Effects

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Radical Reactivity: Concentration Effects 1:20

20.10: Radical Reactivity: Concentration Effects

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Radical Reactivity: Electrophilic Radicals 1:02

20.11: Radical Reactivity: Electrophilic Radicals

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Radical Reactivity: Nucleophilic Radicals 1:16

20.12: Radical Reactivity: Nucleophilic Radicals

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Radical Reactivity: Intramolecular vs Intermolecular 1:33

20.13: Radical Reactivity: Intramolecular vs Intermolecular

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Radical Autoxidation 1:20

20.14: Radical Autoxidation

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Radical Oxidation of Allylic and Benzylic Alcohols 1:21

20.15: Radical Oxidation of Allylic and Benzylic Alcohols

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Radical Substitution: Halogenation of Alkanes and Alkyl Substituents 1:27

20.16: Radical Substitution: Halogenation of Alkanes and Alkyl Substituents

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Radical Halogenation: Thermodynamics 1:34

20.17: Radical Halogenation: Thermodynamics

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Radical Halogenation: Stereochemistry 1:33

20.18: Radical Halogenation: Stereochemistry

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Radical Substitution: Allylic Chlorination 1:31

20.19: Radical Substitution: Allylic Chlorination

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Radical Substitution: Allylic Bromination 1:27

20.20: Radical Substitution: Allylic Bromination

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Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride 1:26

20.21: Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride

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Radical Anti-Markovnikov Addition to Alkenes: Overview 1:25

20.22: Radical Anti-Markovnikov Addition to Alkenes: Overview

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Radical Anti-Markovnikov Addition to Alkenes: Mechanism 1:17

20.23: Radical Anti-Markovnikov Addition to Alkenes: Mechanism

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Radical Anti-Markovnikov Addition to Alkenes: Thermodynamics 1:32

20.24: Radical Anti-Markovnikov Addition to Alkenes: Thermodynamics

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Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview 1:27

20.25: Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview

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Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction 1:22

20.26: Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction

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α-Hydroxy Ketones via Reductive Coupling of Esters: Acyloin Condensation Overview 1:19

20.27: α-Hydroxy Ketones via Reductive Coupling of Esters: Acyloin Condensation Overview

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Chapter 21

Synthetic Polymers

20 Videos · 23 Minutes

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