Compared to benzene, how reactive is nitrobenzene?

Answer 1

Nitrobenzene is LESS reactive than benzene.

The nitro group, #-N^(+)(=O)O^-# is formally electron withdrawing. And the resonance structure suggests this by placing the quaternized nitrogen directly next to the benzene ring. The result? Nitrobenzene is much less reactive in aromatic electrophilic substitution reactions.
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Answer 2

Nitrobenzene is less reactive than benzene due to the presence of the nitro group, which is an electron-withdrawing group that deactivates the benzene ring towards electrophilic aromatic substitution reactions.

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

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