Chad's Videos - Organic Chemistry
Chad's Organic Chemistry Master Course
Quizzes, Study Guides, Chapter Tests, Final Exam Reviews, Practice Final Exams, and More!
Amazing
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This course is an epitome of excellence.
I have been using Chad Videos for over a year and they are spectacular when it comes to understanding mechanisms and IUPAC. The videos are coherent, and concise.
An Answer to my prayers...
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Organic Chemistry
Hi! Just wanted to say thank you, Chad! You are amazing, you make organic chemistry easier and enjoyable! You are a life saver!!! Words can`t describe how grateful I am for you! God bless you!!
Amazing
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The best preparation course
I think he is the best aspect of the course. The lectures were well-organized and clearly presented. Chad's Ultimate Organic Chemistry course is the most necessary and beneficial to students who wants to do well in the subject of Organic Chemistry.
Chad's Organic Chemistry Videos
Chad's Video Lectures Covering a Full Year of Organic Chemistry
Absolutely FREE!
Over 20 hours of video lectures
Covers 22 Chapters
Course Content
- 8.0 Naming Alkenes
- 8.1 Introduction to Alkene Addition Reactions
- 8.2 Hydrohalogenation
- 8.3 Hydration of Alkenes
- 8.4 Addition of Alcohols
- 8.5 Catalytic Hydrogenation
- 8.6 Halogenation of Alkenes and Halohydrin Formation
- 8.7 Epoxidation, Anti Dihydroxylation, and Syn Dihydroxylation
- 8.8 Predicting the Products of Alkene Addition Reactions
- 8.9 Oxidative Cleavage Ozonolysis and Permanganate Cleavage
- *11.1 Functional Group Conversions
- *11.2 Increasing the Length of the Carbon Skeleton
- *11.3 Decreasing the Length of the Carbon Chain or Opening a Ring
- *11.4a Common Patterns in Synthesis Part 1
- *11.4b Common Patterns in Synthesis Part 2
- *11.4c Common Patterns in Synthesis Part 3
- *11.4d Common Patterns in Synthesis Part 4
- 12.1 Properties and Nomenclature of Alcohols
- 12.2 Acidity of Alcohols and Phenols
- 12.3a Synthesis of Alcohols; Reduction of Ketones and Aldehydes
- 12.3b Synthesis of Alcohols; Grignard Addition
- 12.4 Protecting Alcohols
- 12.5a Reaction with HCl, HBr, and HI
- 12.5b Substitution with PBr3 and SOCl2
- 12.5c Formation of Tosylate Esters
- 12.6 Elimination Dehydration
- 12.7 Oxidation with Chromic Acid and PCC
- 14.1 Introduction to IR Spectroscopy
- 14.2a IR Spectra of Carbonyl Compounds
- 14.2b The Effect of Conjugation on the Carbonyl Stretching Frequency
- 14.3 Interpreting More IR Spectra
- 14.4 Introduction to Mass Spectrometry
- 14.5 Isotope Effects in Mass Spectrometry
- 14.6a Fragmentation Patterns of Alkanes, Alkenes, and Aromatic Compounds
- 14.6b Fragmentation Patterns of Alkyl Halides, Alcohols, and Amines
- 14.6c Fragmentation Patterns of Ketones and Aldehydes
- 15.1 Introduction to NMR
- 15.2 The Number of Signals in C 13 NMR
- 15.3 The Number of Signals in Proton NMR
- 15.4 Homotopic vs Enantiotopic vs Diastereotopic
- 15.5a The Chemical Shift in C 13 and Proton NMR
- 15.5b The Integration or Area Under a Signal in Proton NMR
- 15.5c The Splitting or Multiplicity in Proton NMR
- 15.6a Interpreting NMR Example 1
- 15.6b Interpreting NMR Example 2
- 15.6c Interpreting NMR Example 3
- 15.6d Structural Determination From All Spectra Example 4
- 15.6e Structural Determination From All Spectra Example 5
- 15.7 Complex Splitting
- 16.1 Introduction to Conjugated Systems and Heats of Hydrogenation
- 16.2a Introduction to Pi Molecular Orbitals Ethylene
- 16.2b Pi Molecular Orbitals 1,3 Butadiene
- 16.2c Pi Molecular Orbitals the Allyl System
- 16.2d Pi Molecular Orbitals 1,3,5 Hexatriene
- 16.3 UV Vis Spectroscopy
- 16.4 Addition Reactions to Conjugated Dienes
- 16.5a Introduction to Diels Alder Reactions
- 16.5b Stereoselectivity and Regioselectivity in Diels Alder Reactions
- 16.5c Diels Alder Reactions with Cyclic Dienes
- 16.5d Conservation of Orbital Symmetry in Diels Alder Reactions
- 16.6 Cycloaddition Reactions
- 16.7 Electrocyclic Reactions
- 16.8 Sigmatropic Rearrangements
- 18.1 Introduction to Aromatic Substitution Reactions
- 18.2a EAS Bromination and Chlorination
- 18.2b EAS Sulfonation and Desulfonation
- 18.2c EAS Nitration
- 18.2d EAS Friedel Crafts Alkylation and Acylation
- 18.2e EAS Activating and Deactivating Groups and Ortho Para and Meta Directors
- 18.2f EAS Predicting the Products of EAS Reactions
- 18.3 Catalytic Hydrogenation and the Birch Reduction
- 18.4a Side Chain Oxidation with Permanganate or Chromic Acid
- 18.4b Benzylic Bromination with NBS
- 18.4c The Clemmensen and Wolff Kishner Reductions
- 18.4d Side Chain General Reduction
- 18.5 Nucleophilic Aromatic Substitution
- 19.1 Nomenclature of Ketones and Aldehydes
- 19.2 Synthesis of Ketones and Aldehydes
- 19.3 Introduction to Nucleophilic Addition Reactions
- 19.4 Hydration Addition of Water
- 19.5a Addition of Alcohols
- 19.5b Cyclic Acetals as Protecting Groups
- 19.6a Addition of Primary Amines Imine Formation
- 19.6b Addition of Secondary Amines Enamine Formation
- 19.6c Mechanism for the Wolff Kishner Reduction
- 19.7 Reduction via Thioacetals
- 19.8 Hydride Reduction Reactions
- 19.9a Addition of Acetylide Ions and Grignard Reagents
- 19.9b Addition of HCN Cyanohydrin Formation
- 19.9c The Wittig Reaction
- 19.10 Baeyer Villiger Oxidation
- 20.1 Introduction to and Physical Properties of Carboyxylic Acids and Acid Derivatives
- 20.2a Nomenclature of Carboxylic Acids
- 20.2b Nomenclature of Acid Halides
- 20.2c Nomenclature of Acid Anhydrides
- 20.2d Nomenclature of Esters
- 20.2e Nomenclature of Amides
- 20.2f Nomenclature of Nitriles
- 20.3 Introduction to Nucleophilic Acyl Substitution
- 20.4 Reaction with Organometallic Reagents
- 20.5 Hydride Reduction
- 20.6 Interconversion of Carboxylic Acids and Derivatives
- 20.7 The Mechanisms of Nucleophilic Acyl Substitution
- 20.8a Synthesis of Acid Halides
- 20.8b Reactions of Acid Halides
- 20.9 Synthesis and Reactions of Acid Anhydrides
- 20.10a Synthesis of Esters
- 20.10b Reactions of Esters
- 20.11 Synthesis and Reactions of Carboxylic Acids
- 20.12 Synthesis and Reactions of Amides
- 20.13 Synthesis and Reactions of Nitriles
- 21.1 Acidity of the Alpha Hydrogen
- 21.2 General Mechanisms of Alpha Substitution Reactions
- 21.3a Alpha Halogenation
- 21.3b The Haloform Reaction
- 21.3b The HVZ Reaction
- 21.4a Alpha Alkylation
- 21.4b The Stork Synthesis
- 21.5a Introduction to Aldol Reactions
- 21.5b Mechanisms of Aldol Reactions
- 21.5c Mixed Aldol Reactions
- 21.5d Intramolecular Aldol Reactions
- 21.6a Claisen Condensation Reactions
- 21.6b Dieckmann Condensation Reactions
- 21.7a Beta Decarboxylation
- 21.7b The Malonic Ester Synthesis
- 21.7c The Acetoacetic Ester Synthesis
- 21.8 Michael Reactions
- 21.9 The Robinson Annulation
- 22.1 Classification of Amines
- 22.2 Nomenclature of Amines
- 22.3 Basicity of Amines
- 22.4a Synthesis of Amines Reduction
- 22.4b Synthesis of Amines Hofmann Rearrangement
- 22.4c Synthesis of Amines Curtius Rearrangement and Schmidt Reaction
- 22.4d Synthesis of Amines Gabriel Synthesis
- 22.4e Synthesis of Amines Reductive Amination
- 22.5 Acylation
- 22.6 Hofmann Elimination
- 22.7 Cope Elimination
- 22.8a Reaction with Nitrous Acid and the Sandmeyer Reactions
- 22.8b Azo Coupling
- 22.9 EAS Reactions with Nitrogen Heterocycles
Summary of Organic Reactions
SN1, SN2, E1, and E2 Reactions

Alkene Addition Reactions Guide

Alkene Reactions

Alkyne Reactions

Radical Reactions

Alcohol Reactions

Ether Reactions

Epoxide Reactions

Thiol and Sulfide Reactions

Reactions of Aromatic Compounds

Aldehyde and Ketone Reactions

Hydride Reduction Reactions

Organometallic Reactions

Interconversion of Carboxylic Acids and Acid Derivatives

Acyl Halide Reactions

Acid Anhydride Reactions

Ester Reactions

Carboxylic Acid Reactions

Amide Reactions

Nitrile Reactions

Enol and Enolate Reactions (Alpha Substitution Reactions)

Amine Reactions
