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

Onalee S.

I learned more from watching Chad's videos and doing his review quizzes than I ever have from other review sites/ books. He explains things in such a way that they just "click."

This course is an epitome of excellence.

Kyle B.

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...

Ursula H.

Chad is the best instructor! As a non-traditional student I love this course! He helps me understand in a way that the university professors could never! These courses are truly an answer to my prayers! Chad is awesome!

Organic Chemistry

Andreea N.

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

Aida R.

I owe it all to you Chad! the material is explained so so well! I love watching these videos before going to lecture as well as watching them to clear up a lot of the concepts covered in the textbook assigned to me.

Chad is saving my chem courses!

Tabby S.

I just want to say thank you, because this course is the only thing that I needed for my ochem course!

The best preparation course

Amy A.

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

Watch First Lesson

Course Content

Chapter 1 – Electrons, Bonding, and Molecular Properties
- 1.1 Lewis Structures
- 1.2 Formal Charges
- 1.3 Valence Bond Theory and Hybridization
- 1.4 Molecular Orbital Theory
- 1.5 Polarity
- 1.6 Intermolecular Forces
Chapter 2 – Molecular Representations and Resonance
- 2.1 Condensed Structures
- 2.2 Bond Line Structures
- 2.3 Functional Groups
- 2.4 Resonance
Chapter 3 – Acids and Bases
- 3.1 Introduction to Acids and Bases
- 3.2 Ranking Acids and Bases
Chapter 4 – Alkanes
- 4.1 Naming Alkanes
- 4.2 Naming Complex Substituents
- 4.3 Naming Bicyclic Compounds
- 4.4 Drawing Constitutional Isomers
- 4.5 Newman Projections
- 4.6 Cycloalkanes and Cyclohexane Chair Conformations
Chapter 5 – Isomers and Stereochemistry
- 5.1 Overview of Isomerism
- 5.2 Absolute Configurations | How to Assign R and S
- 5.3 Molecules with Multiple Chiral Centers
- 5.4 Fischer Projections
- 5.5 Determining the Relationship Between a Pair of Molecules
- 5.6 Amine Inversion and Chiral Molecules Without Chiral Centers
- 5.7 Optical Activity
Chapter 6 – Organic Reactions and Mechanisms
- 6.1 Reaction Enthalpies and Bond Dissociation Energies
- 6.2 Entropy, Gibbs Free Energy, and the Equilibrium Constant
- 6.3 The Kinetics of Organic Reactions
- 6.4 Nucleophiles, Electrophiles, and Intermediates
- 6.5 Reaction Mechanisms and Curved Arrow Pushing
Chapter 7 – Substitution and Elimination Reactions
- 7.1 SN2 Reactions
- 7.2 SN1 Reactions
- 7.3 SN1 vs SN2
- 7.4 Introduction to Elimination Reactions [Zaitsev’s Rule and the Stability of Alkenes]
- 7.5 E2 Reactions
- 7.6 E1 Reactions and E1 vs E2
- 7.7 Distinguishing Between SN1/SN2/E1/E2
Chapter 8 – Alkenes
- 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
Chapter 9 – Alkynes
- 9.1 Naming Alkynes
- 9.2 Acidity of Alkynes
- 9.3 Synthesis of Alkynes
- 9.4 Reduction of Alkynes
- 9.5 Hydrohalogenation of Alkynes
- 9.6 Halogenation of Alkynes
- 9.7 Hydration of Alkynes
- 9.8 Ozonolysis of Alkynes
- 9.9 Alkylation of Acetylide Ions
Chapter 10 – Radical Reactions
- 10.1 Free Radical Halogenation
- 10.2 The Free Radical Halogenation Mechanism
- 10.3 Allylic and Benzylic Bromination with NBS
- 10.4 Addition of HBr and Peroxide
Chapter 11 – Organic Synthesis (Retrosynthesis)
- 11.1 Introduction to Organic Synthesis
- 11.2 Common Patterns in Organic Synthesis (Involving Alkenes)
- 11.3 Common Patterns in Organic Synthesis (involving Alkynes)
Chapter 12 – Alcohols
- 12.1 Naming Alcohols
- 12.2 Properties of Alcohols
- 12.3 Synthesis of Alcohols
- 12.4 Grignard Reagents
- 12.5 Protecting Alcohols
- 12.6 Substitution Reactions of Alcohols
- 12.7 Elimination Reactions (Dehydration) of Alcohols
- 12.8 Oxidation of Alcohols
- 12.9 Organic Synthesis with Alcohols
Chapter 13 – Ethers, Epoxides, Thiols, and Sulfides
- 13.1 Naming Ethers
- 13.2 Synthesis of Ethers
- 13.3 Reactions of Ethers
- 13.4 Nomenclature of Epoxides
- 13.5 Synthesis of Epoxides
- 13.6 Ring Opening of Epoxides
- 13.7 Nomenclature, Synthesis, and Reactions of Thiols
- 13.8 Nomenclature, Synthesis, and Reactions of Sulfides
- 13.9 Organic Synthesis with Ethers and Epoxides
Chapter 14 – IR Spectroscopy and Mass Spectrometry
- 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
Chapter 15 – NMR Spectroscopy
- 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
Chapter 16 – Conjugated Pi Systems
- 16.1 Introduction to Conjugated Systems and Heats of Hydrogenation
- 16.2a Pi Molecular Orbitals 1,3 Butadiene
- 16.2b Pi Molecular Orbitals the Allyl System
- 16.2c Pi Molecular Orbitals 1,3,5 Hexatriene
- 16.3 UV Vis Spectroscopy
- 16.4 Electrophilic Addition to Conjugated Dienes
- 16.5 Diels Alder Reactions
- 16.6 Cycloaddition Reactions
- 16.7 Electrocyclic Reactions
- 16.8 Sigmatropic Rearrangements
Chapter 17 – Aromatic Compounds
- 17.1 Nomenclature of Benzenes
- 17.2a Criteria for Aromatic Compounds
- 17.2b Aromatic vs Nonaromatic vs Antiaromatic
- 17.3 The Effects of Aromaticity on SN1 Reactions and Acidity Basicity
- 17.4 Aromaticity and Molecular Orbital Theory
Chapter 18 – Reactions of Aromatic Compounds
- 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
Chapter 19 – Ketones and Aldehydes
- 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
Chapter 20 – Carboxylic Acids and Acid Derivatives
- 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
Chapter 21 – Substitution Reactions at the Alpha Carbon
- 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
Chapter 22 – Amines
- 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