In the nitration of aniline, the first equilibrium is established quickly with majority of starting material as the ammonium salt, shown below. Why is the product not entirely m-nitroaniline?  The rate of reaction of aniline is much faster than protonated aniline The ammonium group is a strong deactivator and directs meta. The amino group is a strong activator and directs meta The nitro group is a strong deactivator and directs meta. Steric effects limit the amount of ortho-nitro

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In the nitration of aniline, the first equilibrium is established quickly with majority of starting material as the ammonium salt, shown below. Why is the product not entirely m-nitroaniline?  The rate of reaction of aniline is much faster than protonated aniline The ammonium group is a strong deactivator and directs meta. The amino group is a strong activator and directs meta The nitro group is a strong deactivator and directs meta. Steric effects limit the amount of ortho-nitro
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