1 IUPAC Nomenclature of Alkanes: Part 1
2 IUPAC Nomenclature of Alkanes: Part 2
3 IUPAC Nomenclature of Haloalkanes and Alcohols
4 IUPAC Nomenclature of Alkenes and Alkynes
5 IUPAC Nomenclature of Cyclic Compounds
6 Resonance Structures/Assigning Formal Charge
7 Conformational Analysis of Ethane and Butane - Newman Projections
8 Cyclohexane Chairs
9 Stereochemistry: Enantiomers
10 Cahn-Ingold-Prelog Convention (Determining R/S)
11 Stereochemistry: Meso Compounds, Diastereomers
12 Nucleophiles, Electrophiles, Leaving Groups, and the SN2 Reaction
13 SN1 Reaction
14 E2 Reaction
15 E1 Reaction
16 Choosing Between SN1/SN2/E1/E2 Mechanisms
17 E2 on Cyclic Systems
18 Zaitsev and Hofmann Elimination Products
19 E/Z Absolute Configuration of Alkenes
20 Carbocation Rearrangement - Hydride and Methanide Shifts
21 Addition Reactions
22 Hydrohalogenation, Hydration, Dihalogenation
23 Addition on Conjugated Polyunsaturated Systems
24 Hydrogenation of Alkynes
25 Halohydrin Formation
26 Oxymercuration-Demercuration
27 Hydroboration-Oxidation
28 Alkyne Synthesis by Double Dehydrohalogenation
29 Williamson Ether Synthesis
30 Diels-Alder Cycloaddition
31 Ozonolysis
32 Oxidation and Reduction
33 Aldol Condensation
34 Michael Addition
35 Robinson Annulation
36 Regioselective Enolization and Thermodynamic vs. Kinetic Control
37 Claisen Condensation and Dieckmann Condensation
38 Reactions of Beta-Dicarbonyl Compounds
39 Aromaticity and Huckel's Rule
40 Free Radicals
41 Free Radical Halogenation
42 Anti-Markovnikov Hydrohalogenation
43 Electrophilic Aromatic Substitution
44 Friedel-Crafts Alkylation
45 Friedel-Crafts Acylation
46 Ortho/Meta/Para Directors
47 Clemmensen Reduction
48 Grignard Reaction
49 Wittig Reaction
50 IR Spectroscopy
51 NMR Spectroscopy
52 Homotopic, Enantiotopic, Diastereotopic, and Heterotopic Protons
53 Mass Spectrometry
54 Reactions of Epoxides
55 Hemiacetals, Acetals, and Imines
56 Retrosynthetic Analysis
57 Leaving Group Derivatives
58 Protecting Groups
59 Nomenclature of Polycyclic Compounds: Naphthalene, Biphenyl, Anthracene, Spiro, Bicyclo
60 More Examples Using the Cahn-Ingold-Prelog Convention
61 More Practice With H-NMR Spectra
62 Chiral Molecules With No Chiral Centers
63 Separating Components of a Mixture by Extraction
64 Thin Layer Chromatography (TLC)
65 Column Chromatography
66 Separating Liquids by Distillation
67 Recrystallization
68 Nucleophilic Aromatic Substitution
69 Carboxylic Acids and Their Derivatives
70 Carbonic Acid Derivatives
71 Properties of Amides
72 Assigning R/S on Fischer Projections
73 Fischer Esterification and Saponification
74 Organolithium Reagents
75 Organocuprates (Gilman Reagents)
76 Stereospecificity vs. Stereoselectivity and Regiospecificity vs. Regioselectivity
77 Oxidation of Alkenes Using Potassium Permanganate (Hot and Cold Conditions)
78 Hofmann Elimination via Exhaustive Methylation of Amines
79 Beckmann Rearrangement
80 Baeyer-Villiger Oxidation
81 Allylic/Benzylic Bromination With N-Bromo Succinimide (NBS)
82 Reduction of Esters With DIBAL-H
83 Cleavage of Carbon-Carbon Bonds With Periodic Acid
84 The Haloform Reaction
85 Carbenes Part 1: Properties and Formation
86 Carbenes Part 2: Cyclopropanation, C-H Insertion, and the Bamford-Stevens Reaction
87 Diazomethane Synthesis and Applications (Arndt-Eistert Homologation)
88 The Chemistry of Arynes (Benzyne)
89 Heterocycles Part 1: Furan, Thiophene, and Pyrrole
90 Heterocycles Part 2: Pyridine
91 Pericyclic Reactions Part 1: Revisiting the Diels-Alder Reaction
92 Pericyclic Reactions Part 2: Hetero-DA Reactions and 1,3-Dipolar Cycloadditions
93 Pericyclic Reactions Part 3: Sigmatropic Shifts (Cope Rearrangement, Claisen Rearrangement)
94 Pericyclic Reactions Part 4: Electrocyclizations (Conrotatory/Disrotatory and Nazarov Cyclizations)
95 Gabriel Amine Synthesis
96 Strecker Amino Acid Synthesis