The alcohol homologous series has the general formula CnH2n+1OH.
Primary, secondary and tertiary alcohols
An alcohol can be primary, secondary or tertiary, depending on which carbon atom the hydroxyl group -OH is bonded to.
Primary alcohols are given the notation 1° and the -OH group is attached to a carbon with one alkyl group attached.
Secondary alcohols are given the notation 2° and the -OH group is attached to a carbon with two alkyl groups attached.
Tertiary alcohols are given the notation 3° and the -OH group is attached to a carbon with three alkyl groups attached.
Examples of Primary, secondary and tertiary alcohols
Physical properties of alcohols
Alcohols are polar molecules due to the electronegative hydroxyl group which pulls the electrons in the C-OH bond away from the carbon atom.
The hydroxyl group (-OH) is also polar, with a delta- charge on the oxygen atom and a delta+ charge on the hydrogen atom.
The partial positive charge on the hydrogen atom in the hydroxyl group can attract the lone pairs on an oxygen from a neighbouring molecule, forming hydrogen bonds.
Physical properties of alcohols (2)
When you mix an alcohol with water, hydrogen bonds form between the -OH group and H2O.
If it's a small alcohol (e.g. methanol, ethanol or propan-1-ol), hydrogen bonding lets it mix freely with water- it's soluble in water.
In larger alcohols, most of the molecule is a non-polar carbon chain, so there's less attraction for the polar H2O molecules.
This means that as alcohols increase in size, their solubility in water decreases.
Physical properties of alcohols (3)
Alcohols also form hydrogen bonds with each other.
Hydrogen bonding is the strongest kind of intermolecular force, so it gives alcohols a relatively low volatility (they don't evaporate easily into a gas) and relatively high boiling points compared to non-polar compounds of similar sizes, e.g. alkanes.