Name the following alcohols, utilizing IUPAC nomenclature rules.
a. The longest carbon chain that contains the alcohol functional group has six carbons. When we change the -e to -ol, hexane becomes hexanol. Numbering the chain from the end nearest the —OH group identifi es carbon number 3 as the location of both the —OH group and a methyl group. The complete name is 3-methyl-3-hexanol.
\quad\quad\quad\quad\quad\quad \ \ CH_{3} \\ \overset{1}{C}H_{3}-\overset{2}{C}H_{2}-\overset{3|}{\underset{|}{C}} -\overset{4}{C}H_{2}-\overset{5}{C}H_{2}-\overset{6}{C}H_{3}\\ \quad\quad\quad\quad\quad\quad \ \ OHb. The longest carbon chain containing the —OH group has four carbon atoms. It is numbered from the end closest to the —OH group as follows:
The base name is 1-butanol. The complete name is 2-ethyl-1-butanol.
c. This alcohol is a cyclohexanol. The carbon to which the —OH group is attached is assigned the number 1. The complete name for this alcohol is 3,4- dimethylcyclohexanol. Note that the number 1 is not part of the name.
d. This alcohol is a dimethylheptanol. Numbering from right to left, the location of the hydroxyl group is 1, and locants for the methyl groups are 3 and 4. The complete IUPAC name is 3,4-dimethyl-1-heptanol.
In the naming of alcohols with unsaturated carbon chains, two endings are needed: one for the double or triple bond and one for the hydroxyl group. The -ol suffix always comes last in the name; that is, unsaturated alcohols are named as alkenols or alkynols.
\underset{ \quad\quad {2-Propen-1-ol} \\ {(common name: allyl alcohol)}}{\overset{3}{C}H_{2}=\overset{2}{C}H-\overset{1}{C}H_{2}-OH}The contrast between IUPAC and common names for alcohols is as follows:
IUPAC (one word)
\boxed{alkanol}ethanol
Common (two words)
\boxed{alkyl alcohol}
ethyl alcohol