When naming substituted benzenes, number the ring to give the lowest possible numbers to the substituents. Identify the principal functional groups and the longest carbon chain in the substituent.
To determine the IUPAC name of isoprenaline, we need to analyze its structure. The benzene ring has two hydroxyl groups at positions 1 and 2, making it a benzene-1,2-diol (also known as catechol). The ethylamine substituent is attached to the benzene ring at position 4. The ethylamine group has a hydroxyl group at position 1 and an isopropylamino group at position 2. Therefore, the complete IUPAC name is 4-[1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol.
Let's break down the name:
- "benzene-1,2-diol" indicates the catechol ring.
- The substituent on the benzene ring is at the 4th position.
- The substituent is an ethyl group (-CH2-CH2-) with a hydroxyl group on the first carbon attached to the benzene ring (1-hydroxyethyl-) and an isopropylamino group (-NH-CH(CH3)2) on the second carbon (2-(isopropylamino)ethyl-).
Combining these, we get 4-[1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol.