9: Reactions of Alkyl Halides
- Page ID
- 337968
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- 9.2: Alkyl Halide Reactivity - Substitution Reactions
- 9.2.1: Physical Properties of Haloalkanes
- 9.2.2: Nucleophilic Substitution
- 9.2.3: Reaction Mechanisms Involving Polar Functional Groups- Using "Electron-Pushing'" Arrows
- 9.2.4: A Closer Look at the Nucleophilic Substitution Mechanism- Kinetics
- 9.2.5: Frontside or Backside Attack? Stereochemistry of the SN2 Reaction
- 9.2.6: Consequences of Inversion in SN2 Reactions
- 9.2.7: Structure and \(S_N2\) Reactivity- The Leaving Group
- 9.2.8: Structure and SN2 Reactivity- The Nucleophile
- 9.2.9: Keys to Success- Choosing Among Multiple Mechanistic Pathways
- 9.2.10: Reaction Mechanisms Involving Polar Functional Groups- Using "Electron-Pushing\\'" Arrows
- 9.2.11: Structure and SN2 Reactivity- The Substrate
- 9.2.12: The Sn2 Reaction at a Glance
- 9.2.13: Stereochemical Consequences of SN1 Reactions
- 9.2.14: Stereochemical Consequences of SN1 Reactions
- 9.2.15: Effect of the Alkyl Group on the SN 1 Reaction- Carbocation Stability
- 9.2.E: Properties and Reactions of Haloalkanes- Bimolecular Nucleophilic Substitution (Exercises)
- 9.6: Videos
- The OER Remixer is a self-service tool to rapidly assemble a LibreText from existing sources. This tutorial will include both an explanation of the User Interface as well as a walkthrough of how to do basic tasks.