7: Alkyl Halides and Nucleophilic Substitution Last updated Jun 23, 2019 Save as PDF 6.16: Kinetics 7.1: Introduction to Alkyl Halides Page ID30380 ( \newcommand{\kernel}{\mathrm{null}\,}\) Topic hierarchy7.1: Introduction to Alkyl Halides7.2: Nomenclature7.3: Physical Properties7.4: Interesting Alkyl Halides7.5: The Polar Carbon–Halogen Bond7.6: General Features of Nucleophilic Substitution7.7: The Leaving Group7.8: The Nucleophile7.9: Possible Mechanisms for Nucleophilic Substitution7.10: Two Mechanisms for Nucleophilic Substitution7.11: The \(S_{N}2\) Mechanism7.12: Application- Useful \(S_{N}2\) Reactions7.13: The \(S_{N}1\) Mechanism7.14: Carbocation Stability7.15: The Hammond Postulate7.16: Application- \(S_{N}1\) Reactions, Nitrosamines, and Cancer7.17: When Is the Mechanism \(S_{N}1\) or \(S_{N}2\)?7.18: Vinyl Halides and Aryl Halides7.19: Organic Synthesis