Electrophilic aromatic substitutions proceed in two stages. Attack of the aromatic ring on the electrophile. Regeneration of the stable aromatic system by loss of a positively charged unit, usually a proton. Draw one resonance structure for the intermediate formed when the electrophile is attacked by benzene in the reaction above. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading.