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Chapter 16 Ethers, Epoxides, and Sulfides

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1 Chapter 16 Ethers, Epoxides, and Sulfides
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 2

2 16.1 Nomenclature of Ethers, Epoxides, and Sulfides
2

3 Substitutive IUPAC Names of Ethers
name as alkoxy derivatives of alkanes CH3OCH2 CH3 CH3CH2OCH2CH2CH2Cl methoxyethane 1-chloro-3-ethoxypropane CH3CH2OCH2 CH3 ethoxyethane 3

4 Functional Class IUPAC Names of Ethers
Name the groups attached to oxygen in alphabetical order as separate words; "ether" is last word. CH3OCH2 CH3 CH3CH2OCH2CH2CH2Cl ethyl methyl ether 3-chloropropyl ethyl ether CH3CH2OCH2 CH3 diethyl ether 3

5 Substitutive IUPAC Names of Sulfides
Name as alkylthio derivatives of alkanes. CH3SCH2 CH3 SCH3 methylthioethane (methylthio)cyclopentane CH3CH2SCH2 CH3 ethylthioethane 3

6 Functional Class IUPAC Names of Sulfides
Analogous to ethers, but replace “ether” as last word in the name by “sulfide.” CH3SCH2 CH3 SCH3 ethyl methyl sulfide cyclopentyl methyl sulfide CH3CH2SCH2 CH3 diethyl sulfide 3

7 Oxirane (Ethylene oxide) Oxetane Oxolane (tetrahydrofuran)
Names of Cyclic Ethers O O O Oxirane (Ethylene oxide) Oxetane Oxolane (tetrahydrofuran) Oxane (tetrahydropyran) 1,4-Dioxane O O O 3

8 Names of Cyclic Sulfides
Thiirane Thietane Thiolane Thiane S 3

9 16.2 Structure and Bonding in Ethers and Epoxides
bent geometry at oxygen analogous to water and alcohols 8

10 Bond angles at oxygen are sensitive to steric effects
H H CH3 H 112° 105° 108.5° 132° O (CH3)3C O C(CH3)3 CH3 CH3 9

11 An oxygen atom affects geometry in much the same way as a CH2 group
Most stable conformation of diethyl ether resembles that of pentane. 10

12 An oxygen atom affects geometry in much the same way as a CH2 group
Most stable conformation of tetrahydropyran resembles that of cyclohexane. 10

13 16.3 Physical Properties of Ethers
11

14 Table 16.1 Ethers resemble alkanes more than alcohols with respect to boiling point
Intermolecular hydrogen bonding possible in alcohols; not possible in alkanes or ethers. 36°C 35°C O 117°C OH 12

15 solubility in water (g/100 mL)
Table 16.1 Ethers resemble alcohols more than alkanes with respect to solubility in water solubility in water (g/100 mL) very small 7.5 Hydrogen bonding to water possible for ethers and alcohols; not possible for alkanes. O 9 OH 12


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