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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
Description:
Learn Organic Chemistry with Professor Dave! Together we will go through the main topics in this course, including IUPAC nomenclature, conformational analysis, stereoisomerism, as well as a survey of a variety of organic reactions. Use these videos to supplement your Organic Chemistry course!
Organic Chemistry
Professor Dave Explains
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