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@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.Oxidise hoke kya banega ?
the agents aren't strong enough and-OH is stablized by R so it won't disrupt that stability so it's kind of thermodynamically unfavourable
the -OH in phenol isn’t oxidized here because it's super stable due to resonance with the benzene ring. Plus, the acids mainly do electrophilic substitution and not oxidation. If oxidation were to happen you'd need a way stronger oxidizing agent. So nothin happens with oH while the nitro or nitroso groups get added to the ring.
yeah exactly
Ok,got it,thanks
+solved @Nephilim @itsav23
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