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Benzene (C6H6) exhibits resonance structures that explain its unique stability and aromaticity, characterized by identical carbon-carbon bond lengths of 1.39 Å. The molecule is a resonance hybrid of two Kekulé structures with alternating single and double bonds, leading to delocalized π electrons across the ring. This delocalization results in a bond order of 1.5 for each carbon-carbon bond and contributes to benzene

Author

biswaranjanjena4080

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EN