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Date: 26-2-2016
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Date: 23-7-2019
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Ethers are compounds having two alkyl or aryl groups bonded to an oxygen atom, as in the formula R1–O–R2. The ether functional group does not have a characteristic IUPAC nomenclature suffix, so it is necessary to designate it as a substituent. To do so the common alkoxy substituents are given names derived from their alkyl component (Table 1.1):
Alkyl Group | Name | Alkoxy Group | Name |
---|---|---|---|
CH3– | Methyl | CH3O– | Methoxy |
CH3CH2– | Ethyl | CH3CH2O– | Ethoxy |
(CH3)2CH– | Isopropyl | (CH3)2CHO– | Isopropoxy |
(CH3)3C– | tert-Butyl | (CH3)3CO– | tert-Butoxy |
C6H5– | Phenyl | C6H5O– | Phenoxy |
The smaller, shorter alkyl group becomes the alkoxy substituent. The larger, longer alkyl group side becomes the alkane base name. Each alkyl group on each side of the oxygen is numbered separately. The numbering priority is given to the carbon closest to the oxgen. The alkoxy side (shorter side) has an "-oxy" ending with its corresponding alkyl group. For example, CH3CH2CH2CH2CH2-O-CH2CH2CH3 is 1-propoxypentane. If there is cis or trans stereochemistry, the same rule still applies.
Example 1.1
Examples of ethers include CH3CH2OCH2CH3, diethyl ether (sometimes referred to as ether), and CH3OCH2CH2OCH3, ethylene glycol dimethyl ether (glyme).
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