Ethers can be regarded as substituted alkanes in which a hydrogen atom is replaced with an alkoxy functional group, –OR, and have the general structure R' – O – R'', where R' and R'' are alkyl groups
Ethers are named as substituted alkanes in which a hydrogen atom is replaced with an alkoxyfunctional group (-OR)
The alkoxy group is named by adding the ending ‘oxy’ to the alkyl substituent, and this prefixes the name of the longest carbon chain
Ethers can be prepared in a nucleophilic substitution reaction by reacting a monohaloalkane with an alkoxide
Due to the lack of hydrogen bonding between ether molecules, they have lower boiling points than the corresponding isomeric alcohols.
Smaller GFM ethers (Methoxymethane and methoxyethane) are soluble in water. Larger ethers are insoluble in water due to their increased molecular size (GFM).
Ethers are commonly used as solvents since they are relatively inert chemically and will dissolve many organic compounds.