Basic Organic Nomenclature


Ethers

1) Named as an alkyl alkyl ether:

Ethers are characterized by two alkyl groups being bonded to a central oxygen atom (i.e. R-O-R). The alkyl groups need not be the same, and may contain other function groups. Unfortunately there are several ways to name ethers. An older, but still common method for simple ethers, is to name it as an alkyl alkyl ether (note the spaces between the words). If the two alkyl groups are the same it is named as a dialkyl ether.

Examples naming simple ethers:

Compound Name
Line Drawing
3D Model
ethyl methyl ether
t-butyl propyl ether
 isopropyl methyl ether
diethyl ether
or ether


2) Named as an alkoxy- substituent:

The most common way of naming ethers is as an alkoxy substituent on a parent chain (or ring). This is the common method when one of the alkyl groups is a small simple group, while the other is complex containing multiple substituents or multiple bonds. In this case the smaller of the two alkyl groups is named as the alkoxy substituent, with its location indicated by the numbering scheme of the parent chain (or ring). A few examples of naming alkoxy ethers:
Compound Name
Line Drawing
3-methoxy-1-propene
2-ethoxy-2,4-dimethylpentane
isopropoxycycloheptane
1-methyl-4-sec-butoxycyclohexene


3) Named as an -oxa- substituent:

The final way to name ethers is as an oxa substituent. This method only applies to very complex molecules, where neither of the alkyl groups can be named as simple hydrocarbons, or to complex cyclic ethers. A few examples of naming oxa ethers:
Compound Name
Line Drawing
7-chloro-2,3,4,8-tetramethyl-6-oxadecane
7-ethyl-4,8-dimethyl-6-oxa-2,4-nonadiene


Sulfides

Sulfides are the sulfur analog of ethers. They contain a sulfur atom bonded to two alkyl groups (i.e. R-S-R). They are named as an alkyl alkyl sulfide similar to the simple ethers.

A few examples of naming sulfides:

Compound Name
Line Drawing
ethyl methyl sulfide
dimethyl sulfide
sec-butyl propyl sulfide


Tutorial Quiz: Ethers

Next Page: Amines

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