Benzene typically undergoes
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The bond angle in benzene is
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The electrophile in nitration of benzene is
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Nitration of benzene requires
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Enthalpy of hydrogenation of cyclohexene is −120 kJ mol⁻¹ and of benzene −208 kJ mol⁻¹. By how much (kJ mol⁻¹) is benzene more stable than the Kekulé structure?
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Evidence that benzene doesn't have alternating single and double bonds:
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In the bromination of benzene, FeBr₃ acts as
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Benzene + ethanoyl chloride with AlCl₃ gives
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Methylbenzene heated with alkaline KMnO₄, then acidified, gives
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Methyl groups direct incoming electrophiles to positions
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Methylbenzene + Cl₂ in UV light gives mainly
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7.80 g of benzene ( 78.0) gives 9.84 g of nitrobenzene ( 123). Calculate the percentage yield.
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