Organic Chemistry

Incarcat la data: 19 Aprilie 2011

Autor: Admin

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By Salman Khan - Khan Academy
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Course Description:
Topics covered in college organic chemistry course. Understanding of basic high school or college chemistry assumed.
Lectures:

Lecture 1 - Representing Structures of the Organic Molecules

Representing Structures of Organic Molecules.

Lecture 2 - Naming Sample Alkanes

Naming Simple Alkanes.

Lecture 3 - Naming Alkanes with Alkyl Groups

Naming Alkanes with Alkyl Groups.

Lecture 4 - Correction-2-Propylheptane Should Never Be the Name

Correction - 2-Propylheptane should never be the name!

Lecture 5 - Common and Systematic

Common and Systematic Naming-Iso, Sec and Tert Prefixes

Lecture 6 - More Organic Chemistry Naming

More Organic Chemistry Naming Examples 1.

Lecture 7 - Organic Chemistry Naming Examples 2

Organic Chemistry Naming Examples 2.

Lecture 8 - Organic Chemistry Naming Examples 3

Organic Chemistry Naming Examples 3.

Lecture 9 - Organic Chemistry Naming Examples 4

Organic Chemistry Naming Examples 4.

Lecture 10 - Organic Chemistry Naming Examples 5

Organic Chemistry Naming Examples 5.

Lecture 11 - Naming Alkenes Examples

Naming Alkenes Examples.

Lecture 12 - Naming Alkyl Halides

Naming Alkyl Halides.

Lecture 13 - sp3 Hybridized Orbitals and Sigma

sp3 Hybridized Orbitals and Sigma Bonds.

Lecture 14 - Pi Bonds and sp2 Hybridzied Orbitals

Pi bonds and sp2 Hybridized Orbitals.

Lecture 15 - Newman Projections

Newman Projections.

Lecture 16 - Newman Projections 2

Newman Projections 2.

Lecture 17 - Chair and Boat Shapes for Cyclohexane

Chair and Boat Shapes for Cyclohexane.

Lecture 18 - Double Newman Diagram for Methcyclohexane

Double Newman Diagram for Methcyclohexane.

Lecture 19 - Introduction to Chirality

Introduction to Chirality.

Lecture 20 - Chiral Examples 1

Chiral Examples 1.

Lecture 21 - Chiral Examples 2

Chiral Examples 2.

Lecture 22 - Cahn-Ingold-Prelog System for Naming Enantiomers

Cahn-Ingold-Prelog System for Naming Enantiomers.

Lecture 23 - R,S (Cahn-Ingold-Prelog) Naming System Example 2

R,S (Cahn-Ingold-Prelog) Naming System Example 2.

Lecture 24 - Stereoisomers, Enantiomers, Diastereomers, Constitutional Isomers and Meso Compounds

Stereoisomers, Enantiomers, Diastereomers, Constitutional Isomers and Meso Compounds.

Lecture 25 - Cis-Trans and E-Z Naming Scheme for Alkenes

Cis-Trans and E-Z Naming Scheme for Alkenes.

Lecture 26 - Entgegen-Zusammen Naming Scheme for Alkenes Examples

Entgegen-Zusammen Naming Scheme for Alkenes Examples.

Lecture 27 - Introduction to Reaction Mechanisms

Introduction to Reaction Mechanisms. Addition reaction to an alkene.

Lecture 28 - Markovnikov's Rule and Carbocations

Markovnikov's Rule and Carbocations. Figuring out which addition reaction is more likely.

Lecture 29 - Addition of Water (Acid-Catalyzed) Mechanism

Addition of Water (Acid-Catalyzed) Mechanism.

Lecture 30 - Polymerization of Alkenes with Acid

Polymerization of Alkenes with Acid.

Lecture 31 - Sn2 Reactions

Sn2 Reactions.

Lecture 32 - Sn1 Reactions

Sn1 Reactions.

Lecture 33 - Steric Hindrance

Steric Hindrance.

Lecture 34 - Sn2 Stereochemistry

Sn2 Stereochemistry.

Lecture 35 - Solvent Effects on Sn1 and Sn2 Reactions

Solvent Effects on Sn1 and Sn2 Reactions.

Lecture 36 - Nucleophilicity (Nucleophile Strength)

Nucleophilicity (Nucleophile Strength).

Lecture 37 - Nucleophilicity vs. Basicity

Nucleophilicity vs. Basicity . The difference between what it means to be a nucleophile and a base.

Lecture 38 - E2 Reactions

E2 Elimination Reactions

Lecture 39 - E1 Reactions

E1 Elimination Reactions.

Lecture 40 - Zaitsev's Rule

Zaitsev's Rule for E2 and E1 reactions.

Lecture 41 - Comparing E2 E1 Sn2 Sn1 Reactions

Comparing E2 E1 Sn2 Sn1 Reactions.

Lecture 42 - E2 E1 Sn2 Sn1 Reactions Example 2

E2 E1 Sn2 Sn1 Reactions Example 2.

Lecture 43 - E2 E1 Sn2 Sn1 Reactions Example 3

E2 E1 Sn2 Sn1 Reactions Example 3.

Lecture 44 - Free Radical Reactions

Free radical reactions.

Lecture 45 - Alcohols

Naming alcohols.

Lecture 46 - Alcohol Properties

Alcohol Properties.

Lecture 47 - Resonance

Resonance in benzene and the carbonate ion.

Lecture 48 - Ether Naming and Introduction

Ether Naming and Introduction.

Lecture 49 - Cyclic Ethers and Epoxide Naming

Cyclic ethers and epoxide naming.

Lecture 50 - Ring-opening Sn2 Reaction of Expoxides

Ring-opening Sn2 reaction of expoxides.

Lecture 51 - Sn1 and Sn2 Epoxide Opening Discussion

Sn1 and Sn2 epoxide opening discussion.

Lecture 52 - Aromatic Compounds and Huckel's Rule

Aromatic Compounds and Huckel's Rule.

Lecture 53 - Naming Benzene Derivatives Introduction

Naming Benzene Derivatives Introduction.

Lecture 54 - Electrophilic Aromatic Substitution

Electrophilic Aromatic Substitution.

Lecture 55 - Bromination of Benzene

Bromination of benzene catalyzed by iron bromide.

Lecture 56 - Amine Naming Introduction

Amine Naming Introduction.

Lecture 57 - Amine Naming 2

Amine Naming 2.

Lecture 58 - Amine as Nucleophile in Sn2 Reaction

Amine as Nucleophile in Sn2 Reaction.

Lecture 59 - Amine in Sn2 Part 2

Amine continuing to act as nucleophile to generate more products.

Lecture 60 - Sn1 Amine Reaction

Sn1 Amine Reaction.

Lecture 61 - Aldehyde Introduction

Aldehyde introduction.

Lecture 62 - Ketone Naming

Ketone Naming.

Lecture 63 - Friedel Crafts Acylation

Friedel Crafts Acylation.

Lecture 64 - Friedel Crafts Acylation Addendum

Friedel Crafts Acylation Addendum.

Lecture 65 - Keto Enol Tautomerization

Keto Enol Tautomerization.

Lecture 66 - Carboxlic Acid Introduction

Carboxlic Acid Introduction.

Lecture 67 - Carboxylic Acid Naming

Carboxylic Acid Naming.

Lecture 68 - Fisher Esterification

Fisher Esterification of Carboxylic Acids.

Lecture 69 - Acid Chloride Formation

Acetic Acid to Acetyl Chloride mechanism. Can be generalized to forming any acid halide from a carboxylic acid.

Lecture 70 - Amides, Anhydrides, Esters and Acyl Chlorides

Carboxylic Acid Derivatives - Amides, Anhydrides, Esters and Acyl Chlorides.

Lecture 71 - Relative Stability of Amides Esters Anhydrides and Acyl Chlorides

Relative Stability of Amides Esters Anhydrides and Acyl Chlorides

Lecture 72 - Amide Formation from Acyl Chloride

Amide Formation from Acyl Chloride.

Lecture 73 - Aldol Reaction

Aldol Reaction.

Source: http://academicearth.org/courses/organic-chemistry-khan

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Organic Chemistry