The reactions listed in the question involve different reagents and conditions, each causing specific transformations in the aromatic compounds. Here is the step-by-step breakdown of the transformations:
1. A (Phenol + Zn):
- The reaction of phenol with zinc (\(Zn\)) at elevated temperatures typically leads to the reduction of the hydroxyl group (\(-OH\)) and the formation of benzene.
- Hence, A corresponds to Benzene (II).
2. B (Phenol with Na\(_2\)Cr\(_2\)O\(_7\)/H\(_2\)SO\(_4\)):
- This reaction is an oxidation reaction where phenol undergoes oxidation by chromic acid (\(Na_2Cr_2O_7\)/\(H_2SO_4\)), forming Benzquinone (I) as a product.
3. C (Phenol with CHCl\(_3\)/NaOH, followed by H\(^+\)):
- The reaction of phenol with chloroform (\(CHCl_3\)) and sodium hydroxide (\(NaOH\)) followed by acidification leads to the formation of Salicylaldehyde (IV), which is an aldehyde derivative of phenol.
4. D (Phenol with NaOH, followed by \((ii) CO_2\) under H\(^+\)):
- This reaction involves the formation of Salicylic acid (III) through a Kolbe-Schmitt reaction, where phenol is first treated with sodium hydroxide and then carbon dioxide is added under acidic conditions to produce the carboxylated derivative.
Thus, the correct matching is:
- A - II (Benzene from phenol + Zn)
- B - I (Benzquinone from phenol with Na\(_2\)Cr\(_2\)O\(_7\))
- C - IV (Salicylaldehyde from phenol with CHCl\(_3\)/NaOH)
- D - III (Salicylic acid from phenol with NaOH and CO\(_2\))
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