2,4,6-Trinitrochlorobenzene on warming with water produces:

The hydrolysis of p-chloromitrobenzene requiries it to be heated with NaOH solution at 170^(@)C but the hydrolysis of 1-chloro-2,4,6-trinitribenzene requires only warming with water. Explain these observations.

How will you carry out the following conversions?2,4,6-trinitrochlorobenzene to 2,4,6-trinitrophenol

Which out of o-chloronitrobenzene and 2, 4, 6-trinitrochlorobenzene is more reactive towards nucleophilic substitution?

Which out of o-chloronitrobenzene and 2, 4, 6-trinitrochlorobenzene is more reactive towards nucleophilic substitution?

Which out of o-chloronitrobenzene and 2, 4, 6-trinitrochlorobenzene is more reactive towards nucleophilic substitution?

Write the main products when 2, 4, 6-trinitrochlorobenzene is subjected to hydrolysis.

Write the main product when. 2, 4, 6- trinitrochlorobenzene is sujected to hydrolysis.