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1. A Review of General Chemistry5h 9m
Summary
23m
Intro to Organic Chemistry
5m
Atomic Structure
16m
Wave Function
9m
Molecular Orbitals
17m
Sigma and Pi Bonds
9m
Octet Rule
12m
Bonding Preferences
12m
Formal Charges
6m
Skeletal Structure
14m
Lewis Structure
20m
Condensed Structural Formula
15m
Degrees of Unsaturation
15m
Constitutional Isomers
14m
Resonance Structures
46m
Hybridization
28m
Molecular Geometry
16m
Electronegativity
22m
2. Molecular Representations1h 14m
3. Acids and Bases2h 45m
4. Alkanes and Cycloalkanes4h 19m
IUPAC Naming
29m
Alkyl Groups
13m
Naming Cycloalkanes
10m
Naming Bicyclic Compounds
10m
Naming Alkyl Halides
7m
Naming Alkenes
3m
Naming Alcohols
8m
Naming Amines
15m
Cis vs Trans
21m
Conformational Isomers
13m
Newman Projections
14m
Drawing Newman Projections
16m
Barrier To Rotation
7m
Ring Strain
8m
Axial vs Equatorial
7m
Cis vs Trans Conformations
4m
Equatorial Preference
14m
Chair Flip
9m
Calculating Energy Difference Between Chair Conformations
17m
A-Values
17m
Decalin
7m
5. Chirality3h 23m
Constitutional Isomers vs. Stereoisomers
9m
Chirality
12m
Test 1:Plane of Symmetry
7m
Test 2:Stereocenter Test
17m
R and S Configuration
43m
Enantiomers vs. Diastereomers
13m
Atropisomers
9m
Meso Compound
12m
Test 3:Disubstituted Cycloalkanes
13m
What is the Relationship Between Isomers?
16m
Fischer Projection
10m
R and S of Fischer Projections
7m
Optical Activity
1m
Enantiomeric Excess
14m
Calculations with Enantiomeric Percentages
6m
Non-Carbon Chiral Centers
8m
6. Thermodynamics and Kinetics1h 22m
7. Substitution Reactions1h 37m
8. Elimination Reactions2h 30m
10. Addition Reactions3h 18m
Addition Reaction
6m
Markovnikov
5m
Hydrohalogenation
6m
Acid-Catalyzed Hydration
17m
Oxymercuration
15m
Hydroboration
26m
Hydrogenation
6m
Halogenation
6m
Halohydrin
12m
Carbene
12m
Epoxidation
8m
Epoxide Reactions
9m
Dihydroxylation
8m
Ozonolysis
7m
Ozonolysis Full Mechanism
24m
Oxidative Cleavage
3m
Alkyne Oxidative Cleavage
6m
Alkyne Hydrohalogenation
3m
Alkyne Halogenation
2m
Alkyne Hydration
6m
Alkyne Hydroboration
2m
11. Radical Reactions1h 58m
12. Alcohols, Ethers, Epoxides and Thiols2h 42m
Alcohol Nomenclature
4m
Naming Ethers
6m
Naming Epoxides
18m
Naming Thiols
11m
Alcohol Synthesis
7m
Leaving Group Conversions - Using HX
11m
Leaving Group Conversions - SOCl2 and PBr3
13m
Leaving Group Conversions - Sulfonyl Chlorides
7m
Leaving Group Conversions Summary
4m
Williamson Ether Synthesis
3m
Making Ethers - Alkoxymercuration
4m
Making Ethers - Alcohol Condensation
4m
Making Ethers - Acid-Catalyzed Alkoxylation
4m
Making Ethers - Cumulative Practice
10m
Ether Cleavage
8m
Alcohol Protecting Groups
3m
t-Butyl Ether Protecting Groups
5m
Silyl Ether Protecting Groups
10m
Sharpless Epoxidation
9m
Thiol Reactions
6m
Sulfide Oxidation
4m
13. Alcohols and Carbonyl Compounds2h 17m
14. Synthetic Techniques1h 26m
15. Analytical Techniques:IR, NMR, Mass Spect6h 50m
Purpose of Analytical Techniques
5m
Infrared Spectroscopy
16m
Infrared Spectroscopy Table
31m
IR Spect:Drawing Spectra
40m
IR Spect:Extra Practice
26m
NMR Spectroscopy
10m
1H NMR:Number of Signals
26m
1H NMR:Q-Test
26m
1H NMR:E/Z Diastereoisomerism
8m
H NMR Table
21m
1H NMR:Spin-Splitting (N + 1) Rule
17m
1H NMR:Spin-Splitting Simple Tree Diagrams
11m
1H NMR:Spin-Splitting Complex Tree Diagrams
8m
1H NMR:Spin-Splitting Patterns
8m
NMR Integration
18m
NMR Practice
14m
Carbon NMR
4m
Structure Determination without Mass Spect
47m
Mass Spectrometry
12m
Mass Spect:Fragmentation
28m
Mass Spect:Isotopes
27m
16. Conjugated Systems5h 34m
Conjugation Chemistry
13m
Stability of Conjugated Intermediates
4m
Allylic Halogenation
12m
Conjugated Hydrohalogenation (1,2 vs 1,4 addition)
26m
Diels-Alder Reaction
9m
Diels-Alder Forming Bridged Products
11m
Diels-Alder Retrosynthesis
8m
Molecular Orbital Theory
9m
Drawing Atomic Orbitals
6m
Drawing Molecular Orbitals
17m
hom*o LUMO
4m
Orbital Diagram:3-atoms- Allylic Ions
13m
Orbital Diagram:4-atoms- 1,3-butadiene
11m
Orbital Diagram:5-atoms- Allylic Ions
10m
Orbital Diagram:6-atoms- 1,3,5-hexatriene
13m
Orbital Diagram:Excited States
4m
Pericyclic Reaction
10m
Thermal Cycloaddition Reactions
26m
Photochemical Cycloaddition Reactions
26m
Thermal Electrocyclic Reactions
14m
Photochemical Electrocyclic Reactions
10m
Cumulative Electrocyclic Problems
25m
Sigmatropic Rearrangement
17m
Cope Rearrangement
9m
Claisen Rearrangement
15m
17. Aromaticity2h 29m
18. Reactions of Aromatics:EAS and Beyond4h 29m
Electrophilic Aromatic Substitution
9m
Benzene Reactions
11m
EAS:Halogenation Mechanism
6m
EAS:Nitration Mechanism
9m
EAS:Friedel-Crafts Alkylation Mechanism
6m
EAS:Friedel-Crafts Acylation Mechanism
5m
EAS:Any Carbocation Mechanism
7m
Electron Withdrawing Groups
22m
EAS:Ortho vs. Para Positions
4m
Acylation of Aniline
9m
Limitations of Friedel-Crafts Alkyation
19m
Advantages of Friedel-Crafts Acylation
6m
Blocking Groups - Sulfonic Acid
12m
EAS:Synergistic and Competitive Groups
13m
Side-Chain Halogenation
6m
Side-Chain Oxidation
4m
Birch Reduction
10m
EAS:Sequence Groups
4m
EAS:Retrosynthesis
29m
Diazo Replacement Reactions
6m
Diazo Sequence Groups
5m
Diazo Retrosynthesis
13m
Nucleophilic Aromatic Substitution
28m
Benzyne
16m
19. Aldehydes and Ketones:Nucleophilic Addition4h 52m
Naming Aldehydes
8m
Naming Ketones
7m
Oxidizing and Reducing Agents
9m
Oxidation of Alcohols
28m
Ozonolysis
7m
DIBAL
5m
Alkyne Hydration
9m
Nucleophilic Addition
8m
Cyanohydrin
11m
Organometallics on Ketones
16m
Overview of Nucleophilic Addition of Solvents
13m
Hydrates
6m
Hemiacetal
9m
Acetal
12m
Acetal Protecting Group
16m
Thioacetal
6m
Imine vs Enamine
15m
Addition of Amine Derivatives
5m
Wolff Kishner Reduction
7m
Baeyer-Villiger Oxidation
39m
Acid Chloride to Ketone
7m
Nitrile to Ketone
9m
Wittig Reaction
18m
Ketone and Aldehyde Synthesis Reactions
14m
20. Carboxylic Acid Derivatives:NAS2h 5m
Carboxylic Acid Derivatives
7m
Naming Carboxylic Acids
9m
Diacid Nomenclature
6m
Naming Esters
5m
Naming Nitriles
3m
Acid Chloride Nomenclature
5m
Naming Anhydrides
7m
Naming Amides
5m
Nucleophilic Acyl Substitution
18m
Carboxylic Acid to Acid Chloride
6m
Fischer Esterification
5m
Acid-Catalyzed Ester Hydrolysis
4m
Saponification
3m
Transesterification
5m
Lactones, Lactams and Cyclization Reactions
10m
Carboxylation
5m
Decarboxylation Mechanism
14m
21. Enolate Chemistry:Reactions at the Alpha-Carbon1h 53m
Tautomerization
9m
Tautomers of Dicarbonyl Compounds
6m
Enolate
4m
Acid-Catalyzed Alpha-Halogentation
4m
Base-Catalyzed Alpha-Halogentation
3m
Haloform Reaction
8m
Hell-Volhard-Zelinski Reaction
3m
Overview of Alpha-Alkylations and Acylations
5m
Enolate Alkylation and Acylation
12m
Enamine Alkylation and Acylation
16m
Beta-Dicarbonyl Synthesis Pathway
7m
Acetoacetic Ester Synthesis
13m
Malonic Ester Synthesis
15m
22. Condensation Chemistry2h 9m
23. Amines1h 43m
24. Carbohydrates5h 46m
Monosaccharide
20m
Monosaccharides - D and L Isomerism
9m
Monosaccharides - Drawing Fischer Projections
18m
Monosaccharides - Common Structures
6m
Monosaccharides - Forming Cyclic Hemiacetals
12m
Monosaccharides - Cyclization
18m
Monosaccharides - Haworth Projections
13m
Mutarotation
11m
Epimerization
9m
Monosaccharides - Aldose-Ketose Rearrangement
8m
Monosaccharides - Alkylation
10m
Monosaccharides - Acylation
7m
Glycoside
6m
Monosaccharides - N-Glycosides
18m
Monosaccharides - Reduction (Alditols)
12m
Monosaccharides - Weak Oxidation (Aldonic Acid)
7m
Reducing Sugars
23m
Monosaccharides - Strong Oxidation (Aldaric Acid)
4m
Monosaccharides - Oxidative Cleavage
27m
Monosaccharides - Osazones
10m
Monosaccharides - Kiliani-Fischer
23m
Monosaccharides - Wohl Degradation
12m
Monosaccharides - Ruff Degradation
12m
Disaccharide
30m
Polysaccharide
11m
25. Phenols15m
26. Amino Acids, Peptides, and Proteins2h 55m
27. Transition Metals5h 33m
Electron Configuration of Elements
45m
Coordination Complexes
20m
Ligands
24m
Electron Counting
10m
The 18 and 16 Electron Rule
13m
Cross-Coupling General Reactions
40m
Heck Reaction
40m
Stille Reaction
13m
Suzuki Reaction
25m
Sonogashira Coupling Reaction
17m
f*ckuyama Coupling Reaction
15m
Kumada Coupling Reaction
13m
Negishi Coupling Reaction
16m
Buchwald-Hartwig Amination Reaction
19m
Eglinton Reaction
17m