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Combining action :- The N=N bond is used to link two aromatic rings together in the process. In the presence of phenol or aromatic amines, arene diazonium salts—such as benzene diazonium salts—react to produce colored azo compounds.
A diazonium compound and another aromatic compound engage in a chemical process known as an azo coupling, which results in an azo compound. The aryldiazonium cation acts as the electrophile and the activated arene as the nucleophile in this electrophilic aromatic substitution process.
Benzene diazonium chloride and phenol combine to form a yellow-orange azo molecule. The reaction is catalyzed by the base.
As a result, although the reason is flawed, the assertion is true.
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