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ETHERS
John Cedric Malayag
Samantha Elizabeth Sequito
Dessi Raye Tan
Ether comes from the Latin
aether, means “to ignite”.
High vapor pressure at
room temperature, which
makes them very
flammable.
An ether is an organic
compound in which an
oxygen atom is bonded
to two carbon atoms by
single bonds.
STRUCTURAL
CHARACTERISTICS
OF ETHERS
Examples of
Ethers Include:
CHɜ―O―CHɜ
CHɜ―CH2―O—
CHɜ―O—
GENERALIZED
FORMULAS FOR
ETHERS
R—O—R
R—O—R´
R—O—Ar
Ar—O—Ar
Note that unlike alcohols
and phenols, ethers do not
possess a hydroxyl
(—OH) group.
NOMENCLATURE
FOR
ETHERS
LINE-ANGLE
STRUCTURAL
FORMULAS FOR
SELECTED
SIMPLE ETHERS
Ethyl methyl ether
(methoxyethane)
Diethyl ether
(ethoxyethane)
Dipropyl ether
(1 – propxypropane)
Unsymmetrical
Ethers
Ether in the molecule
of which the two
ligands on the ether
group are different.
Name both hydrocarbon groups
bonded to the oxygen atom in
alphabetical order and add the word
ether, separating the words with a
space.
CHɜ—O—CH2—CHɜ
Ethyl methyl ether
CHɜ—CH2—O—
Ethyl phenyl ether
Symmetrical
Ethers
Ether in the
molecule of which
the two ligands on
the ether group are
identical.
Name the alkyl group, add the
prefix di- , and then add the word
ether, separating the words with a
space.
CHɜ—O—CHɜ
Dimethyl ether
CHɜ—CH2—O—CH2—CHɜ
Diethyl ether
ALKOXY
GROUP
Is an — OR group, an akyl/aryl
group attached to an oxygen atom.
Examples:
CHɜ—O— CHɜ—CH2—O—
Methoxy group Ethoxy group
CHɜ—CH2—CH2—O—
Propoxy group
RULES FOR
NAMING AN
ETHER USING
THE IUPAC
SYSTEM
Rule 1: Select the longest carbon chain and
use its name as the base name.
Rule 2: Change the –yl ending of the other
hydrocarbon group to –oxy to obtain the
alkoxy group name; methyl becomes
methoxy, ethyl becomes ethoxy, etc.
Rule 3: Place the alkoxy name with a
locator number, infront of the base chain
name.
EXAMPLES OF
IUPAC ETHER
NOMENCLATUR
E
CHɜ—O—CH2—CH2—CH2—CHɜ
1 - Methoxybutane
CHɜ—CH—CH2—O—CH2—CHɜ
|
CHɜ
1- Ethoxy – 2-methylproprane
O—CHɜ
O—CHɜ
Anisole
CH2—CH=CH2
Anethole
ISOMERIS
M FOR
ETHERS
Ethers contain two
carbon chains (two alkyl
groups), unlike the one
carbon chain found in
alcohols.
There are
Three C4
Ether
Constitutional
CHɜ—CH2—O—CH2—CHɜ
Diethyl ether
CHɜ—O—CH2—CH2—CH2—CHɜ
Methyl propyl ether
CHɜ—O—CH—CHɜ
CHɜ
Isopropyl methyl ether
FUNCTIONAL
GROUP
ISOMERISM
Are constitutional
isomers that contain
different functional
groups.
CHɜ—CH2—O—CHɜ
Ethyl methyl ether
CHɜ—CH2—CH2—OH
Propyl alcohol
CHɜ—CH—OH
CHɜ
Isopropyl alcohol
PHYSICAL
AND
CHEMICAL
PROPERTIES
The boiling points of ethers
are similar to those of
alkanes of comparable
molecular mass and are much
lower than those of alcohols
of comparable molecular
mass.
Alkane
CHɜ—CH2—CH2—CH2—CHɜ
Mol. Mass = 72 amu bp=36°C
Ether
CHɜ—CH2—O—CH2—CHɜ
Mol. Mass = 74 amu bp=35°C
Alcohol
CHɜ—CH2—CH2—CH2—OH
Mol. Mass = 74 amu bp=117°C
The much higher boiling
point of the alcohol results
from hydrogen bonding
between alcohol molecules.
Gas
Liquid
Ether are more soluble
in water than are alkanes
Similar to alcohols of
the same molecular
mass.
TWO CHEMICAL
PROPERTIES OF
ETHERS ARE
SPECIALLY
IMPORTANT
Ethers are flammable.
Ethers react slowly with
oxygen from the air to
form unstable
hydroperoxides and
peroxides.
R—O—O—H
Hydroperoxide
R—O—O—R
Peroxide
CYCLIC
ETHERS
Cyclic ethers
contain ether
functional groups as
part of a ring system.
ETHYLENE
OXIDE
TETRAHYDROFURAN
(THF)
FURAN
PYRAN
HETEROCYCLIC
ORGANIC
COMPOUND
Is a cyclic organic
compound in which one
or more of the carbon
atoms in the ring have
been replaced with atoms
of other elements.

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Ethers