Organic Chemistry Complete Course

1.1 Lewis Structures | Organic Chemistry Complete Course
1.2 Formal Charges | Organic Chemistry
1.3 Valence Bond Theory and Hybridization | Organic Chemistry
1.4 Molecular Orbital Theory (MO Theory) | Organic Chemistry
1.5 Polarity | Organic Chemistry
1.6 Intermolecular Forces | Organic Chemistry
2.1 Condensed Structures | Organic Chemistry
2.2 Drawing Line Angle Structures (aka Bond Line Structures) | Organic Chemistry
2.3 Identifying Functional Groups | Organic Chemistry
2.4 Resonance | Organic Chemistry
3.1 Introduction to Acids and Bases | Organic Chemistry
3.2 Ranking Acids and Bases | Organic Chemistry
4.1 IUPAC Nomenclature of Alkanes and Cycloalkanes | Organic Chemistry
4.2 Naming Complex Substituents | Organic Chemistry
4.3 IUPAC Nomenclature of Bicyclic Compounds | Organic Chemistry
4.4 Drawing Structural Isomers | Organic Chemistry
4.5 Newman Projections | Organic Chemistry
4.6 Cycloalkanes and Cyclohexane Chair Conformations | Organic Chemistry
5.1 Overview of Isomers | Constitutional Isomers and Stereoisomers | Organic Chemistry
5.2 How to Assign R and S Configuration | Absolute Configuration | Organic Chemistry
5.3 Molecules with Multiple Chiral Centers | Enantiomers, Diastereomers, and Meso Compounds | OChem
5.4 Fischer Projections | Organic Chemistry
5.5 How to Identify Type of Isomerism | Organic Chemistry
5.6 Amine Inversion and Chiral Molecules without Chiral Centers (Allene & Biphenyl) | Organic
5.7 Optical Activity | Organic Chemistry
6.1 Reaction Enthalpy and Bond Dissociation Energy | Organic Chemistry
6.2 Entropy, Gibbs Free Energy, and the Equilibrium Constant | Organic Chemistry
6.3 The Kinetics of Organic Reactions | Organic Chemistry
6.4 Nucleophiles, Electrophiles, and Intermediates | Organic Chemistry
6.5 Curved Arrow Pushing in Reaction Mechanisms | Organic Chemistry
7.1 SN2 Reaction | Organic Chemistry
7.2 SN1 Reactions | Organic Chemistry
7.3 SN1 vs SN2 | Organic Chemistry
7.4 Introduction to Elimination Reactions [Zaitsev's Rule and the Stability of Alkenes] | OChemistry
7.5 E2 Reactions | Organic Chemistry
7.6 E1 Reactions and E1 vs E2 | Organic Chemistry
7.7 How to Distinguish Between Substitution and Elimination Reactions (SN2 SN1 E2 E1) | OChem
8.0 Naming Alkenes IUPAC | Organic Chemistry
8.1 Introduction to Alkene Addition Reactions; Markovnikov's Rule and Syn vs Anti | OChemistry
8.2 Hydrohalogenation of Alkenes | Organic Chemistry
8.3 Acid Catalyzed Hydration, Oxymercuration Demercuration, and Hydroboration Oxidation | OChemistry
8.4 Addition of an Alcohol | Acid-Catalyzed Addition and Alkoxymercuration-Demercuration | OChem
8.5 Catalytic Hydrogenation of Alkenes and Heats of Hydrogenation | Organic Chemistry
8.6 Halogenation of Alkenes and Halohydrin Formation | Organic Chemistry
8.7 Expoxidation, Anti-Dihydroxylation, and Syn-Dihydroxylation of Alkenes | Organic Chemistry
8.8 How to Predict the Products of Alkene Addition Reactions | Organic Chemistry
8.9 Ozonolysis of Alkenes, Oxidation of Alkenes with KMnO4 | Oxidative Cleavage | Organic Chemistry
9.1 Naming Alkynes | Organic Chemistry
9.2 Acidity of Alkynes | Organic Chemistry
9.3 Synthesis of Alkynes | Organic Chemistry
9.4 Reduction of Alkynes | Organic Chemistry
9.5 Hydrohalogenation of Alkynes | Organic Chemistry
9.6 Halogenation of Alkynes | Organic Chemistry
9.7 Hydration of Alkynes | Organic Chemistry
9.8 Ozonolysis of Alkynes | Organic Chemistry
9.9 Alkylation of Acetylide Ions from Terminal Alkynes | Organic Chemistry
10.1 Free Radical Halogenation | Organic Chemistry
10.2 The Free Radical Halogenation Mechanism | Organic Chemistry
10.3 Allylic Bromination and Benzylic Bromination with NBS | Organic Chemistry
10.4 Addition of HBr and Peroxide | Organic Chemistry
11.1 Introduction to Organic Synthesis | Retrosynthesis | Organic Chemistry
11.2 Common Patterns in Organic Synthesis Involving Alkenes | Retrosynthesis | Organic Chemistry
11.3 Common Patterns in Organic Synthesis Involving Alkynes | Organic Chemistry
12.1 Naming Alcohols | Organic Chemistry
12.2 Properties of Alcohols | Organic Chemistry
12.3 Synthesis of Alcohols | Organic Chemistry
12.4 Grignard Reagents | Organic Chemistry
12.5 Protecting Groups for Alcohols | Organic Chemistry
12.6 Substitution Reactions of Alcohols | Organic Chemistry
12.7 Elimination Reactions of Alcohols | Organic Chemistry
12.8 Oxidation of Alcohols by Chromic Acid and PCC | Organic Chemistry
12.9 Organic Synthesis with Alcohols | Organic Chemistry
13.1 Naming Ethers | Organic Chemistry
13.2 Synthesis of Ethers | Organic Chemistry
13.3 Reactions of Ethers | Organic Chemistry
13.4 Naming Epoxides | Organic Chemistry
13.5 Synthesis of Epoxides | Organic Chemistry
13.6 Ring Opening of Epoxides | Organic Chemistry
13.7 Thiols | Organic Chemistry
13.8 Sulfides | Organic Chemistry
13.9 Organic Synthesis with Ethers and Epoxides | Retrosynthesis | Organic Chemistry
14.1 Introduction to IR Spectroscopy | Organic Chemistry
14.2a IR Spectra of Carbonyl Compounds | Organic Chemistry
14.2b The Effect of Conjugation on the Carbonyl Stretching Frequency | Organic Chemistry
14.3 Interpreting More IR Spectra | Organic Chemistry
14.4 Introduction to Mass Spectrometry | Organic Chemistry
14.5 Isotope Effects in Mass Spectrometry | Organic Chemistry
14.6a Fragmentation Patterns of Alkanes, Alkenes, and Aromatic Compounds | Mass Spectrometry
14.6b Fragmentation Patterns of Alkyl Halides, Alcohols, and Amines | Mass Spectrometry
14.6c Fragmentation Patterns of Ketones and Aldehydes | Mass Spectrometry
15.1 Introduction to NMR | Organic Chemistry
15.2 The Number of Signals in C 13 NMR | Organic Chemistry
15.3 The Number of Signals in Proton NMR | Organic Chemistry
15.4 Homotopic vs Enantiotopic vs Diastereotopic | Organic Chemistry
15.5a The Chemical Shift in C 13 and Proton NMR | Organic Chemistry
15.5b The Integration or Area Under a Signal in Proton NMR | Organic Chemistry
15.5c The Splitting or Multiplicity in Proton NMR | Organic Chemistry
15.6a Interpreting NMR Example 1 | Organic Chemistry
15.6b Interpreting NMR Example 2 | Organic Chemistry
15.6c Interpreting NMR Example 3 | Organic Chemistry
15.6d Structural Determination From All Spectra Example 4 | Organic Chemistry
15.6e Structural Determination From All Spectra Example 5 | Organic Chemistry
15.7 Complex Splitting | NMR | Organic Chemistry
16.1 Conjugated Systems and Heats of Hydrogenation | Organic Chemistry
16.2a Pi Molecular Orbitals of 1,3 Butadiene | Organic Chemistry
16.2b Pi Molecular Orbitals of the Allyl System | Organic Chemistry
16.2c Pi Molecular Orbitals of 1,3,5-Hexatriene | Organic Chemistry
16.3 UV/Vis Spectroscopy | Organic Chemistry
16.4 Electrophilic Addition to Conjugated Dienes | Organic Chemistry
16.5 Diels-Alder Reactions | Organic Chemistry
16.6 Cycloaddition Reactions | Organic Chemistry
16.7 Electrocyclic Reactions | Organic Chemistry
16.8 Sigmatropic Rearrangements | Organic Chemistry
17.1 Naming Benzenes | Organic Chemistry
17.2 Aromatic vs Antiaromatic vs Nonaromatic | Organic Chemistry
17.3 The Effects of Aromaticity on Reactivity | Organic Chemistry
17.4 Pi Molecular Orbitals of Benzene | Organic Chemistry
18.1 Electrophilic Aromatic Substitution (EAS Reactions) | Organic Chemistry
18.2 Friedel Crafts Alkylation and Acylation | Organic Chemistry
18.3 Ortho-Para Directors vs Meta Directors in EAS Reactions | Organic Chemistry
18.4 Catalytic Hydrogenation and the Birch Reduction | Organic Chemistry
18.5 Side Chain Reactions of Benzenes | Organic Chemistry
18.6 Nucleophilic Aromatic Substitution (NAS) | Organic Chemistry
18.7 Retrosynthesis with Aromatic Compounds | Organic Chemistry
19.1 Naming Ketones and Aldehydes | Organic Chemistry
19.2 Synthesis of Ketones and Aldehydes | Organic Chemistry
19.3 Introduction to Nucleophilic Addition of Ketones and Aldehydes | Organic Chemistry
19.4a Formation of Hemiacetals and Acetals (Nucleophilic Addition of Alcohols) | Organic Chemistry
19.4b Cyclic Acetals as Protecting Groups for Alcohols | Organic Chemistry
19.5 Imine and Enamine Formation | Addition of Amines | Organic Chemistry
19.6 Reduction of Ketones and Aldehydes (NaBH4 and LiAlH4) | Organic Chemistry
19.7a Addition of Grignard Reagents (and other Carbon Nucleophiles)
19.7b Wittig Reaction | Organic Chemistry
19.8 Baeyer Villiger Oxidation | Organic Chemistry
19.9 Retrosynthesis with Aldehydes and Ketones | Organic Chemistry
20.1 Naming Carboxylic Acids and Carboxylic Acid Derivatives | Organic Chemistry
20.2 Nucleophilic Acyl Substitution | Organic Chemistry
20.3 The Mechanisms of Nucleophilic Acyl Substitution | Organic Chemistry
20.4 Reaction with Grignard Reagents and Gilman Reagents | Carboxylic Acid Derivatives
20.5 Hydride Reduction Reactions | Carboxylic Acid Derivatives | Organic Chemistry
20.6 Synthesis and Reactions of Acid Halides | Organic Chemistry
20.7 Synthesis and Reactions of Acid Anhydrides | Organic Chemistry
20.8 Synthesis and Reactions of Esters | Organic Chemistry
20.9 Properties, Synthesis, and Reactions of Carboxylic Acids | Organic Chemistry
20.10 Synthesis and Reactions of Amides | Organic Chemistry
20.11 Synthesis and Reactions of Nitriles | Organic Chemistry
20.12 Retrosynthesis with Carboxylic Acids Derivatives | Organic Chemistry
21.1 Acidity of the Alpha Hydrogen | Organic Chemistry
21.2 Mechanisms of Alpha Substitution Reactions | Organic Chemistry
21.3 Alpha Halogenation | Organic Chemistry
21.4 Alpha Alkylation | Organic Chemistry
21.5 Aldol Reactions | Organic Chemistry
21.6 Claisen Condensation Reactions | Organic Chemistry
21.7 Malonic Ester Synthesis and Acetoacetic Ester Synthesis | Organic Chemistry
21.8 Michael Reactions | Organic Chemistry
21.9 Robinson Annulation | Organic Chemistry
21.10 Retrosynthesis with Enolates and Enols | Organic Chemistry
22.1 Naming Amines | Organic Chemistry
22.2 Basicity of Amines | Organic Chemistry
22.3 Synthesis of Amines | Organic Chemistry
22.4 Hofmann Elimination and Cope Elimination | Organic Chemistry
22.5 Sandmeyer Reactions | Organic Chemistry
22.6 EAS Reactions with Nitrogen Heterocycles | Organic Chemistry
22.7 Retrosynthesis with Amines | Organic Chemistry
24.1 Classification of Monosaccharides | Organic Chemistry
24.2 Reactions of Monosaccharides | Organic Chemistry
24.3 Disaccharides and Polysaccharides | Organic Chemistry