Let's analyze the structures of catechol and m-cresol:
**Catechol:** Catechol is also known as 1,2-dihydroxybenzene.
It consists of a benzene ring with two hydroxyl (\( -OH \)) groups attached to adjacent carbon atoms (positions 1 and 2).
Therefore, the IUPAC name for catechol is benzene-1,2-diol.
The structure of catechol is:
**m-cresol:** Cresol is the common name for methylphenol.
The prefix "m-" (meta) indicates that the methyl (\( -CH_3 \)) group and the hydroxyl (\( -OH \)) group are attached to the benzene ring at positions 1 and 3 relative to each other.
If we consider the hydroxyl group to be at position 1 (as it gives the phenol base name), then the methyl group is at position 3.
Therefore, the IUPAC name for m-cresol is 3-methylphenol.
The structure of m-cresol is:
Matching these IUPAC names with the options:
Option
(A) Benzene - 1, 4 - diol; 3 - Methoxy phenol: Benzene-1,4-diol is hydroquinone, and 3-methoxy phenol is m-methoxyphenol (not m-cresol).
Option
(B) Benzene - 1, 2 - diol; 3 - Methoxy phenol: Benzene-1,2-diol is catechol, but 3-methoxy phenol is not m-cresol.
Option
(C) Benzene - 1, 3 - diol; 3 - Methyl phenol: Benzene-1,3-diol is resorcinol (not catechol), but 3-methyl phenol is m-cresol.
Option
(D) Benzene - 1, 2 - diol; 3 - Methyl phenol: Benzene-1,2-diol is catechol, and 3-methyl phenol is m-cresol.
Thus, option (D) correctly identifies catechol as benzene-1,2-diol and m-cresol as 3-methyl phenol.