Which one of the following products is formed by the oxidation of phen

Which one of the following products is formed by the oxidation of phenol with chromic acid?

[amp_mcq option1=”1,4-Benzoquinone” option2=”1,2-Benzoquinone” option3=”Benzoic acid” option4=”Diphenyl ether” correct=”option1″]

This question was previously asked in
UPSC Geoscientist – 2023
The correct answer is 1,4-Benzoquinone.
Phenol can be oxidized to quinones. Chromic acid (H₂CrO₄), typically generated in situ from K₂Cr₂O₇ or CrO₃ in acidic solution, is a strong oxidizing agent. Oxidation of phenol with strong oxidizing agents like chromic acid generally results in the formation of p-benzoquinone (1,4-benzoquinone). The hydroxyl group is oxidized, and the aromatic ring is modified to form a conjugated cyclic diketone structure.
1,2-Benzoquinone (o-benzoquinone) is usually formed by milder oxidation methods, such as using Fremy’s salt. Benzoic acid involves cleavage of the ring, which is not the primary product of phenol oxidation with chromic acid under typical conditions. Diphenyl ether (C₆H₅OC₆H₅) is formed through a different type of reaction involving phenol, not simple oxidation.
Exit mobile version