How are alcohols named using the IUPAC system?

Created from Britannica articles using AI. AI can make mistakes, so verify using Britannica articles.

The International Union of Pure and Applied Chemistry (IUPAC) system provides a systematic method for naming alcohols. The process follows these three steps:

  1. Identify the parent chain: Determine the longest carbon chain that contains the carbon atom bonded to the hydroxyl (–OH) group. Use the corresponding alkane name, drop the final "-e," and add the suffix "-ol."
  2. Number the chain: Number the longest carbon chain starting from the end closest to the –OH group. Use this number to indicate the position of the hydroxyl group if necessary.
  3. Name substituents: Identify and name any additional substituents, providing their positions using the same numbering rules applied to alkanes or alkenes.1

For cyclic alcohols, the prefix "cyclo-" is used, and the hydroxyl group is assumed to be on carbon 1. The ring is then numbered to ensure other substituents receive the lowest possible numbers.1