this_is_harsh
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Resonance occurs in nitrobenzene (C6H5NO2) despite the presence of only one pi bond. The discussion highlights that the pi electrons in the nitro group (NO2) are attracted to the benzene ring, facilitating resonance due to the positive charge associated with the nitro group. This interaction contributes to the overall bond strength within the molecule. The presence of conjugated pi bonds is essential for resonance to manifest in nitrobenzene.
PREREQUISITESChemistry students, organic chemists, and anyone interested in understanding molecular interactions and resonance in aromatic compounds.
Your question is not clear. Could you rephrase it?this_is_harsh said:"My teacher had mentioned that resonance would occur here due to the presence of a positive charge if benzene is attached. However, if we consider two bonds without breaking them, there will be one pi bond. So, will there be no resonance due to it?"