Organic Chemistry Khan Academy
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World Mentoring Academy
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Details
Topics covered in college organic chemistry course. Basic understanding of basic high school or college chemistry assumed. Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, composition, reactions,
and preparation (by synthesis or by other means) of carbon-based compounds, hydrocarbons, and their derivatives. These compounds may contain any number of other elements, including hydrogen, nitrogen, oxygen, the halogens as well as phosphorus, silicon, and
sulfur.
Resources: OpenCourseware from Khan Academy, MIT, UC Berkeley, Stanford along with many of the World's finest University's.
Language: English
Professors: Michael Williams
Units: 73
Lesson content
- Representing Structures of Organic Molecules
- Naming Simple Alkanes
- Naming Alkanes with Alkyl Groups
- Correction - 2-Propylheptane should never be the name!
- Common and Systematic Naming-Iso, Sec and Tert Prefixes
- More Organic Chemistry Naming Examples 1
- Organic Chemistry Naming Examples 2
- Organic Chemistry Naming Examples 3
- Organic Chemistry Naming Examples 4
- Organic Chemistry Naming Examples 5
- Naming Alkenes Examples
- Naming Alkyl Halides
- sp3 Hybridized Orbitals and Sigma Bonds
- Pi bonds and sp2 Hybridized Orbitals
- Newman Projections
- Newman Projections 2
- Chair and Boat Shapes for Cyclohexane
- Double Newman Diagram for Methcyclohexane
- Introduction to Chirality
- Chiral Examples 1
- Chiral Examples 2
- Cahn-Ingold-Prelog System for Naming Enantiomers
- R,S (Cahn-Ingold-Prelog) Naming System Example 2
- Stereoisomers, Enantiomers, Diastereomers, Constitutional Isomers and Meso Compounds
- Cis-Trans and E-Z Naming Scheme for Alkenes
- Entgegen-Zusammen Naming Scheme for Alkenes Examples
- Introduction to Reaction Mechanisms
- Markovnikov's Rule and Carbocations : Markovnikov's Rule and Carbocations. Figuring out which additi
- Addition of Water (Acid-Catalyzed) Mechanism
- Polymerization of Alkenes with Acid
- Sn2 Reactions
- Sn1 Reactions
- Steric Hindrance
- Sn2 Stereochemistry
- Solvent Effects on Sn1 and Sn2 Reactions
- Nucleophilicity (Nucleophile Strength)
- Nucleophilicity vs. Basicity . The difference between what it means to be a nucle
- E2 Elimination Reactions
- E1 Elimination Reactions
- Zaitsev's Rule for E2 and E1 reactions
- Comparing E2 E1 Sn2 Sn1 Reactions
- E2 E1 Sn2 Sn1 Reactions Example 2
- E2 E1 Sn2 Sn1 Reactions Example 3
- Free Radical Reactions
- Alcohols : Naming alcohols
- Alcohol Properties
- Resonance in benzene and the carbonate ion
- Ether Naming and Introduction
- Cyclic ethers and epoxide naming
- Ring-opening Sn2 reaction of expoxides
- Sn1 and Sn2 epoxide opening discussion
- Aromatic Compounds and Huckel's Rule
- Naming Benzene Derivatives Introduction
- Electrophilic Aromatic Substitution
- Bromination of Benzene : Bromination of benzene catalyzed by iron bromide
- Amine Naming Introduction
- Amine Naming 2
- Amine as Nucleophile in Sn2 Reaction
- Amine in Sn2 part 2 : Amine continuing to act as nucleophile to generate more products
- Sn1 Amine Reaction
- Aldehyde Introduction
- Ketone Naming
- Friedel Crafts Acylation
- Friedel Crafts Acylation Addendum
- Keto Enol Tautomerization
- Carboxlic Acid Introduction
- Carboxylic Acid Naming
- Fisher Esterification of Carboxylic Acids
- Acid Chloride Formation : Acetic Acid to Acetyl Chloride mechanism. Can be generalized to forming any aci
- Amides, Anhydrides, Esters and Acyl Chlorides : Carboxylic Acid Derivatives - Amides, Anhydrides, Este
- Relative Stability of Amides Esters Anhydrides and Acyl Chlorides
- Amide Formation from Acyl Chloride
- Aldol Reaction
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