Chapter 6
Web Site for Chapter 6
Alkyl Halide Family (R-X)
Nucleophilic Substitutions:Net Reaction
Nucleophiles
Leaving Groups
Nucleophilic Substitutions
Kinetics- SN2
Reaction Mechanism-SN2
Transition State Theory
Stereochemistry-SN2
Reaction Kinetics-SN1
Reaction of t-ButylChloride with Hydroxide ion-SN1
Reaction Mechanism-SN1
Carbocation Intermediates-SN1
Stereochemistry-SN1
Solvolysis-SN1
Factors Affecting Rates of SN1 and SN2 Reactions
Substituent Factor-SN2
Substituent Effect-SN1
Concentration of Nucleophile-SN2
Concentration Effect of Nucleophile-SN1
Nucleophilic Strength-SN2
Nucleophilic Strength-SN1
Solvent Effect-SN2
Solvent Effect-SN1
Leaving Group Ability (LGA)- SN2
Leaving Group Ability(LGA)-SN1
Molecular Rearrangement-SN1
Summary-SN1 vs SN2
Organic Synthesis:Functional Group Transformation-SN2
Phenyl and Vinylic Halides
Elimination Reactions of Alkyl Halides-Dehydrohalogenation
Dehydrohalogenation (1,2 elemination)
Bases Used In Dehydrohalogenation
Elimination Mechanisms
E2 Reaction Mechanism
Elimination-E1
Favorable Conditions-E2
Favorable Conditions-E1
SN vs E Reactions
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