9: Alcohols, Ethers, and Epoxides Last updated Jun 23, 2019 Save as PDF 8.11: When Is the Reaction SN1, SN2, E1, or E2? 9.1: Dehydration Using POCl3 and Pyridine Page ID57494 ( \newcommand{\kernel}{\mathrm{null}\,}\) Topic hierarchy9.1: Dehydration Using \(POCl_{3}\) and Pyridine9.2: Conversion of Alcohols to Alkyl Halides with HX9.3: Conversion of Alcohols to Alkyl Halides with \(SOCl_{2}\) and \(PBr_{3}\)9.4: Tosylate—Another Good Leaving Group9.5: Reaction of Ethers with Strong Acid9.6: Reactions of Epoxides9.7: Application- Epoxides, Leukotrienes, and Asthma9.8: Application- Benzo[a]pyrene, Epoxides, and Cancer9.9: Introduction9.10: Structure and Bonding9.11: Nomenclature9.12: Physical Properties9.13: Interesting Alcohols, Ethers, and Epoxides9.14: Preparation of Alcohols, Ethers, and Epoxides9.15: General Features—Reactions of Alcohols, Ethers, and Epoxides9.16: Dehydration of Alcohols to Alkenes9.17: Carbocation Rearrangements