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Your question is not clear. Could you rephrase it?this_is_harsh said:
Yes, resonance does occur in nitrobenzene despite having one pi bond. The nitro group in nitrobenzene can delocalize the electrons through resonance, leading to a more stable molecule.
Resonance increases the stability of nitrobenzene by delocalizing the electrons within the nitro group. This delocalization spreads the charge over a larger area, making the molecule more stable.
The nitro group in nitrobenzene plays a crucial role in resonance by accepting and donating electrons through its nitrogen and oxygen atoms. This electron delocalization leads to resonance stabilization of the molecule.
Yes, resonance in nitrobenzene can affect its reactivity. The delocalization of electrons through resonance can influence the reactivity of nitrobenzene towards electrophilic aromatic substitution reactions.
The presence of a pi bond in nitrobenzene allows for the delocalization of electrons through resonance, enhancing the stability of the molecule. This delocalization is facilitated by the presence of the nitro group in nitrobenzene.
