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    Lec 37 - Nucleophilicity vs. Basicity

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

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    Tags: Nucleophilicity vs. Basicity

    Uploaded by: ( Send Message ) on 17-09-2012.

    Duration: 12m 47s

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    Lec 38 - E2 Reactions

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    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 18 - Double Newman Diagram for Methcyclohexane

    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 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