Organic Chemistry
Master Organic Chemistry with Chad's Prep: From Lewis Structures to Advanced Reaction Mechanisms! Dive into the world of organic chemistry through engaging lessons and comprehensive explanations. Perfect for students eager to excel!
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What you'll learn
- Understand and apply Lewis structures and formal charge concepts.
- Compare and evaluate SN1 and SN2 reaction mechanisms.
- Name and synthesize carboxylic acids and their derivatives.
- Interpret IR spectra to identify functional groups in organic compounds.
This course includes
- 41.5 hours of video
- Certificate of completion
- Access on mobile and TV
Course content
1 modules • 168 lessons • 41.5 hours of video
Mastering Organic Chemistry: Structures, Reactions, and Synthesis
168 lessons
• 41.5 hours
Mastering Organic Chemistry: Structures, Reactions, and Synthesis
168 lessons
• 41.5 hours
- Drawing Lewis Structures | 1.1 Organic Chemistry 24:19
- Formal Charge | 1.2 Organic Chemistry 07:08
- Valence Bond Theory & Hybridization | 1.3 Organic Chemistry 26:04
- Molecular Orbital Theory | 1.4 Organic Chemistry 22:47
- Polarity | Polar vs Nonpolar | 1.5 Organic Chemistry 12:58
- Intermolecular Forces | Rank Boiling Points | 1.6 Organic Chemistry 32:50
- Condensed Structures | 2.1 Organic Chemistry 12:27
- Bond Line Structures | Line Angle Structures | 2.2 Organic Chemistry 26:44
- Identifying Functional Groups | 2.3 Organic Chemistry 23:42
- Resonance Structures | 2.4 Organic Chemistry 41:58
- Acids and Bases | Definitions, pKa & Acid Strength | 3.1 Organic Chemistry 14:38
- Ranking Acids and Bases | 3.2 Organic Chemistry 35:47
- Naming Alkanes | IUPAC Nomenclature | 4.1 Organic Chemistry 34:45
- Naming Complex Substituents: IUPAC Systematic & Common Names | 4.2 Organic Chemistry 23:17
- Naming Bicyclic Compounds | IUPAC | 4.3 Organic Chemistry 14:48
- Drawing Constitutional Isomers | 4.4 Organic Chemistry 21:00
- Newman Projections | 4.5 Organic Chemistry 13:25
- Cyclohexane Chair Conformations | 4.6 Organic Chemistry 45:30
- Isomers: Structural Isomers vs Stereoisomers | 5.1 Organic Chemistry 36:02
- Assigning R and S Configurations | 5.2 Organic Chemistry 25:23
- Stereoisomers with Multiple Chiral Centers | 5.3 Organic Chemistry 24:30
- Fischer Projections | Assign R & S | 5.4 Organic Chemistry 13:41
- Determine Isomeric Relationships | 5.5 Organic Chemistry 12:54
- Chirality without Chiral Centers & Amine Inversion | 5.6 Organic Chemistry 11:54
- Optical Activity | Specific Rotation | 5.7 Organic Chemistry 16:48
- Reaction Enthalpy & Bond Dissociation Energy | 6.1 Organic Chemistry 12:29
- Thermodynamics for Ochem | Entropy, ΔG, & Keq | 6.2 Organic Chemistry 17:55
- Kinetics of Organic Reactions | 6.3 Organic Chemistry 17:18
- Nucleophiles, Electrophiles, & Intermediates | 6.4 Organic Chemistry 16:09
- Curved Arrow Pushing | 6.5 Organic Chemistry 19:25
- SN2 Reactions | 7.1 Organic Chemistry 29:21
- SN1 Reactions | 7.2 Organic Chemistry 24:45
- SN1 vs SN2 | Nucleophile, Substrate, Solvent | 7.3 Organic Chemistry 21:27
- Intro to Elimination Reactions | E1 & E2 | 7.4 Organic Chemistry 07:44
- E2 Reactions | 7.5 Organic Chemistry 25:54
- E1 Reactions | E1 vs E2 | 7.6 Organic Chemistry 15:26
- SN1 vs SN2 vs E1 vs E2 | 7.7 Organic Chemistry 14:26
- Naming Alkenes | IUPAC Nomenclature | 8.0 Organic Chemistry 18:25
- Intro to Alkene Addition Reactions | Markovnikov's Rule | 8.1 Organic Chemistry 08:37
- Hydrohalogenation of Alkenes | HBr vs HBr/ROOR | 8.2 Organic Chemistry 09:48
- Hydration of Alkenes | Acid-catalyzed, Oxymercuration, Hydroboration | 8.3 Organic Chemistry 24:19
- Alcohol Addition to Alkenes | 8.4 Organic Chemistry 07:18
- Catalytic Hydrogenation of Alkenes | 8.5 Organic Chemistry 08:15
- Halogenation of Alkenes & Halohydrin Formation | 8.6 Organic Chemistry 13:18
- Expoxidation & Syn/Anti-Dihydroxylation of Alkenes | 8.7 Organic Chemistry 08:37
- Predicting Alkene Products | Regio- & Stereoselectivity | 8.8 Organic Chemistry 06:39
- Ozonolysis vs Permanganate Cleavage of Alkenes | 8.9 Organic Chemistry 05:28
- Naming Alkynes | IUPAC Nomenclature | 9.1 Organic Chemistry 06:39
- Acidity of Terminal Alkynes | 9.2 Organic Chemistry 05:27
- Alkyne Synthesis | E2: Geminal vs Vicinal Dihalides | 9.3 Organic Chemistry 08:07
- Reduction of Alkynes | Catalytic, Lindlar's, Dissolving Metal | 9.4 Organic Chemistry 10:37
- Hydrohalogenation of Alkynes | HBr vs HBr/ROOR | 9.5 Organic Chemistry 06:08
- Halogenation of Alkynes | 9.6 Organic Chemistry 02:49
- Hydration of Alkynes: Oxymercuration-Reduction vs Hydroboration-Oxidation | 9.7 Organic Chemistry 17:31
- Ozonolysis of Alkynes | 9.8 Organic Chemistry 03:51
- Acetylide Alkylation | SN2 with Terminal Alkynes | 9.9 Organic Chemistry 03:53
- Free Radical Halogenation | 10.1 Organic Chemistry 13:54
- Free Radical Halogenation Mechanism | 10.2 Organic Chemistry 15:46
- Allylic & Benzylic Bromination with NBS | 10.3 Organic Chemistry 11:18
- Addition of HBr/ROOR Radical Mechanism | 10.4 Organic Chemistry 08:17
- Introduction to Organic Synthesis | Retrosynthesis | 11.1 Organic Chemistry 25:41
- Common Patterns in Organic Synthesis with Alkenes | 11.2 Organic Chemistry 22:36
- Common Patterns in Organic Synthesis with Alkynes | 11.3 Organic Chemistry 26:27
- Naming Alcohols | IUPAC Nomenclature | 12.1 Organic Chemistry 08:36
- Properties of Alcohols | Solubility, b.p., Acidity | 12.2 Organic Chemistry 28:58
- Synthesis of Alcohols | 12.3 Organic Chemistry 22:06
- Grignard Reagents | 12.4 Organic Chemistry 14:09
- Protecting Groups for Alcohols: Silyl Ethers | 12.5 Organic Chemistry 09:23
- Substitution Reactions of Alcohols | 12.6 Organic Chemistry 16:34
- Elimination Reactions of Alcohols | 12.7 Organic Chemistry 18:56
- Oxidation of Alcohols | Chromic Acid vs PCC | 12.8 Organic Chemistry 13:54
- Organic Synthesis with Alcohols | 12.9 Organic Chemistry 17:04
- Naming Ethers | IUPAC Nomenclature | 13.1 Organic Chemistry 03:06
- Synthesis of Ethers | 13.2 Organic Chemistry 05:17
- Reactions of Ethers | 13.3 Organic Chemistry 09:34
- Naming Epoxides | IUPAC Nomenclature | 13.4 Organic Chemistry 04:32
- Synthesis of Epoxides | 13.5 Organic Chemistry 06:59
- Ring Opening of Epoxides | 13.6 Organic Chemistry 11:13
- Thiols | Naming, Synthesis, Reactions | 13.7 Organic Chemistry 06:31
- Sulfides | Naming, Synthesis, Reactions | 13.8 Organic Chemistry 05:34
- Organic Synthesis with Ethers & Epoxides | 13.9 Organic Chemistry 16:45
- Introduction to IR Spectroscopy | 14.1 Organic Chemistry 10:57
- 14.2a IR Spectra of Carbonyl Compounds | Organic Chemistry 06:27
- 14.2b The Effect of Conjugation on the Carbonyl Stretching Frequency | Organic Chemistry 05:58
- 14.3 Interpreting More IR Spectra | Organic Chemistry 06:45
- 14.4 Introduction to Mass Spectrometry | Organic Chemistry 06:19
- 14.5 Isotope Effects in Mass Spectrometry | Organic Chemistry 06:29
- 14.6a Fragmentation Patterns of Alkanes, Alkenes, and Aromatic Compounds | Mass Spectrometry 06:20
- 14.6b Fragmentation Patterns of Alkyl Halides, Alcohols, and Amines | Mass Spectrometry 04:56
- 14.6c Fragmentation Patterns of Ketones and Aldehydes | Mass Spectrometry 03:45
- 15.1 Introduction to NMR | Organic Chemistry 02:46
- 15.2 The Number of Signals in C 13 NMR | Organic Chemistry 04:53
- 15.3 The Number of Signals in Proton NMR | Organic Chemistry 10:38
- 15.4 Homotopic vs Enantiotopic vs Diastereotopic | Organic Chemistry 10:16
- 15.5a The Chemical Shift in C 13 and Proton NMR | Organic Chemistry 08:41
- 15.5b The Integration or Area Under a Signal in Proton NMR | Organic Chemistry 01:47
- 15.5c The Splitting or Multiplicity in Proton NMR | Organic Chemistry 04:55
- 15.6a Interpreting NMR Example 1 | Organic Chemistry 05:10
- 15.6b Interpreting NMR Example 2 | Organic Chemistry 07:43
- 15.6c Interpreting NMR Example 3 | Organic Chemistry 03:54
- 15.6d Structural Determination From All Spectra Example 4 | Organic Chemistry 05:58
- 15.6e Structural Determination From All Spectra Example 5 | Organic Chemistry 08:48
- 15.7 Complex Splitting | NMR | Organic Chemistry 11:42
- Conjugated Pi Electrons | 16.1 Organic Chemistry 13:03
- 1,3-Butadiene Pi Molecular Orbitals | 16.2a Organic Chemistry 20:42
- Allyl System Pi Molecular Orbitals | 16.2b Organic Chemistry 10:27
- 1,3,5-Hexatriene Pi Molecular Orbitals | 16.2c Organic Chemistry 08:25
- UV/Vis Spectroscopy | 16.3 Organic Chemistry 04:27
- Conjugate Diene Addition | Kinetic vs Thermodynamic | 16.4 Organic Chemistry 15:32
- Diels-Alder Reactions | 16.5 Organic Chemistry 46:11
- Cycloaddition Reactions | 16.6 Organic Chemistry 32:46
- Electrocyclic Reactions | 16.7 Organic Chemistry 22:33
- Sigmatropic Rearrangements | 16.8 Organic Chemistry 14:51
- Naming Benzenes | IUPAC Nomenclature | 17.1 Organic Chemistry 12:56
- Aromatic vs Antiaromatic vs Nonaromatic | 17.2 Organic Chemistry 35:21
- Effects of Aromaticity on Reactivity | 17.3 Organic Chemistry 08:34
- Aromatic vs Antiaromatic | 17.4 Organic Chemistry 15:39
- Electrophilic Aromatic Substitution (EAS) | 18.1 Organic Chemistry 23:21
- Friedel Crafts Alkylation & Acylation | 18.2 Organic Chemistry 17:42
- Ortho-Para vs Meta Directors | 18.3 Organic Chemistry 39:57
- Catalytic Hydrogenation vs Birch Reduction | 18.4 Organic Chemistry 05:03
- Benzene Side Chain Reactions | 18.5 Organic Chemistry 16:56
- Nucleophilic Aromatic Substitution (NAS) | 18.6Organic Chem 13:55
- Retrosynthesis with Aromatic Compounds | 18.7 Organic Chemistry 24:28
- Naming Ketones & Aldehydes | IUPAC Nomenclature | 19.1 Organic Chemistry 09:52
- Ketone & Aldehyde Synthesis | 19.2 Organic Chemistry 07:40
- Nucleophilic Addition: Aldehydes vs Ketones | 19.3 Organic Chemistry 13:17
- Hemiacetals & Acetals | Formation & Hydrolysis | 19.4a Organic Chemistry 16:57
- Aldehyde & Ketone Protecting Groups | 19.4b Organic Chemistry 07:28
- Imines & Enamines | 19.5 Organic Chemistry 26:49
- Reduction of Ketones & Aldehydes | NaBH4 vs LiAlH4 | 19.6 Organic Chemistry 11:21
- Grignard Addition to Aldehydes & Ketones | 19.7a Organic Chemistry 07:11
- Wittig Reaction | 19.7b Organic Chemistry 10:37
- Baeyer-Villiger Oxidation | 19.8 Organic Chemistry 06:17
- Retrosynthesis with Aldehydes & Ketones | 19.9 Organic Chemistry 23:07
- Naming Carboxylic Acids and Acid Derivatives | 20.1 Organic Chemistry 10:28
- Nucleophilic Acyl Substitution | 20.2 Organic Chemistry 31:28
- Nucleophilic Acyl Substitution Mechanisms | 20.3 Organic Chemistry 13:16
- Grignard Reagents vs Gilman Reagents | 20.4 Organic Chemistry 05:05
- Hydride Reduction | NaBH4 vs LiAlH4 vs DIBAH | 20.5 Organic Chemistry 10:51
- Acid Halide Synthesis & Reactions | 20.6 Organic Chemistry 05:51
- Acid Anhydride Synthesis & Reactions | 20.7 Organic Chemistry 04:53
- Ester Synthesis & Reactions | 20.8 Organic Chemistry 19:23
- Carboxylic Acid Properties, Synthesis & Reactions | 20.9 Organic Chemistry 13:58
- Amide Synthesis & Reactions | 20.10 Organic Chemistry 04:44
- Nitrile Synthesis & Reactions | 20.11 Organic Chemistry 05:44
- Retrosynthesis with Carboxylic Acids & Derivatives | 20.12 Organic Chemistry 16:58
- Alpha Hydrogen Acidity | Enolates & Enols | 21.1 Organic Chemistry 16:45
- Mechanisms of Alpha Substitution Reactions | 21.2 Organic Chemistry 06:22
- Alpha Halogenation (Haloform Included) | 21.3 Organic Chemistry 12:49
- Alpha Alkylation (Stork Reaction Included) | 21.4 Organic Chemistry 07:01
- Aldol Reactions | 21.5 Organic Chemistry 32:18
- Claisen Condensation Reactions | 21.6 Organic Chemistry 12:15
- Malonic & Acetoacetic Ester Synthesis | 21.7 Organic Chemistry 16:06
- Michael Reactions | 21.8 Organic Chemistry 10:34
- Robinson Annulation | 21.9 Organic Chemistry 08:45
- Retrosynthesis with Enolates & Enols | 21.10 Organic Chemistry 11:26
- Naming Amines | IUPAC Nomenclature | 22.1 Organic Chemistry 06:54
- Basicity of Amines | 22.2 Organic Chemistry 06:28
- Synthesis of Amines | 22.3 Organic Chemistry 23:00
- Hofmann Elimination & Cope Elimination | 22.4 Organic Chemistry 11:57
- Sandmeyer Reactions | 22.5 Organic Chemistry 04:11
- EAS Reactions with Nitrogen Heterocycles | 22.6 Organic Chemistry 08:12
- Retrosynthesis with Amines | 22.7 Organic Chemistry 18:05
- Classification of Monosaccharides | 24.1 Organic Chemistry 26:25
- Reactions of Monosaccharides | 24.2 Organic Chemistry 26:54
- Disaccharides and Polysaccharides | 24.3 Organic Chemistry 12:54
- Amino Acids & Proteins | Organic Chemistry 25 01:14:59
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