benzene diazonium ion reacts with p amino phenol in basic medium gives
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Benzene diazonium chloride on reaction with phenol in a basic medium gives p-Hydroxy azobenzene. This is an example of the coupling reaction.
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When benzene diazonium ion reacts with p amino phenol it gives p-Hydroxy azobenzene
- The aromatic diazonium ion naturally formed from the diazotisation of aniline in common is benzenediazonium. Benzene diazonium chloride properly produces p-Hydroxy azobenzene when reacted with phenol in a ordinary medium.
- The specific substance p-Hydroxy azobenzene is generally an orange coloured dye.
- The active substance is properly produced as a direct result of coupling mechanism.
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