Lec 18 - Double Newman Diagram for Methcyclohexane

Lecture list for this course

Lec 1 - Representing Structures of Organic Molecules

Lec 2 - Naming Simple Alkanes

Lec 3 - Naming Alkanes with Alkyl Groups

Lec 4 - Correction - 2-Propylheptane should never be the name!

Lec 5 - Common and Systematic Naming-Iso, Sec and Tert Prefixes

Lec 6 - More Organic Chemistry Naming Examples 1

Lec 7 - Organic Chemistry Naming Examples 2

Lec 8 - Organic Chemistry Naming Examples 3

Lec 9 - Organic Chemistry Naming Examples 4

Lec 10 - Organic Chemistry Naming Examples 5

Lec 11 - Naming Alkenes Examples

Lec 12 - Naming Alkyl Halides

Lec 13 - sp3 Hybridized Orbitals and Sigma Bonds

Lec 14 - Pi bonds and sp2 Hybridized Orbitals

Lec 15Newman Projections

Lec 16 - Newman Projections 2

Lec 17 - Chair and Boat Shapes for Cyclohexane

Lec 19 - Introduction to Chirality

Lec 20 - Chiral Examples 1

Lec 21 - Chiral Examples 2

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

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

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

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

Lec 26 - Entgegen-Zusammen Naming Scheme for Alkenes Examples

Lec 27 - Introduction to Reaction Mechanisms

Lec 28 - Markovnikov's Rule and Carbocations

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

Lec 30 - Polymerization of Alkenes with Acid

Lec 31 - Sn2 Reactions

Lec 32 - Sn1 Reactions

Lec 33 - Steric Hindrance

Lec 34 - Sn2 Stereochemistry

Lec 35 - Solvent Effects on Sn1 and Sn2 Reactions

Lec 36 - Nucleophilicity (Nucleophile Strength)

Lec 37 - Nucleophilicity vs. Basicity

Lec 38 - E2 Reactions

Lec 39 - E1 Reactions

Lec 40 - Zaitsev's Rule

Lec 41 - Comparing E2 E1 Sn2 Sn1 Reactions

Lec 42 - E2 E1 Sn2 Sn1 Reactions Example 2

Lec 43 - E2 E1 Sn2 Sn1 Reactions Example 3

Lec 44 - Free Radical Reactions

Lec 45 - Alcohols

Lec 46 - Alcohol Properties

Lec 47 - Resonance

Lec 48 - Ether Naming and Introduction

Lec 49 - Cyclic ethers and epoxide naming

Lec 50 - Ring-opening Sn2 reaction of expoxides

Lec 51 - Sn1 and Sn2 epoxide opening discussion

Lec 52 - Aromatic Compounds and Huckel's Rule

Lec 53 - Naming Benzene Derivatives Introduction

Lec 54 - Electrophilic Aromatic Substitution

Lec 55 - Bromination of Benzene

Lec 56 - Amine Naming Introduction

Lec 57 - Amine Naming 2

Lec 58 - Amine as Nucleophile in Sn2 Reaction

Lec 59 - Amine in Sn2 part 2

Lec 60 - Sn1 Amine Reaction

Lec 61 - Aldehyde Introduction

Lec 62 - Ketone Naming

Lec 63 - Friedel Crafts Acylation

Lec 64 - Friedel Crafts Acylation Addendum

Lec 65 - Keto Enol Tautomerization

Lec 66 - Carboxlic Acid Introduction

Lec 67 - Carboxylic Acid Naming

Lec 68 - Fisher Esterification

Lec 69 - Acid Chloride Formation

Lec 70 - Amides, Anhydrides, Esters and Acyl Chlorides

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

Lec 72 - Amide Formation from Acyl Chloride

Lec 73 - Aldol Reaction