If I am not mistaken , p-block is not a compound !
CO is the most common OXIDE reducing agent . Do you expect Sodium oxide to behave as a good reducing agent ?
Almost all reactions are .
Yes . TNT is produced by step by step nitration with increasing temperature and purity of acids .
No problem .
Chloro group is weakly deactivating itself .
In chlorobenzene case , polynitration would be dependent on temperature to an extent but stating...
Of course the lone pair resonance is stronger . Thats why toluene will take harsher conditions than phenol .
And I meant that by your theory , "even weakly acrivating groups will give the reaction" .
Well , giving out the answer directly won't do you good and it would (maybe) be against the forum rules . Think about Le Chateliers principle and the temperature variation of equilibrium constant . You must have surely learned this .
the methyl group activates o-p by HC , if nitration indirectly activates meta position , why shouldn't toluene give trinitration . Since your argument is not based on the activating group , even a weakly activating group should give the rxn .