Solved: Why is o-nitroacetanilide much more soluble in acidic, Basic Statistics

Why is o-nitroacetanilide much more soluble in acidic

The para isomer is formed in the reaction in far greater quantity than the orthodox isomer. Justify this fact.

The ortho isomer is not isolated because it is soluble in the acidic water solution. Why is o-nitroacetanilide much more soluble in acidic aqueous solution than p-nitroacetanilide?

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Basic Statistics: Why is o-nitroacetanilide much more soluble in acidic

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Basic Statistics: Why is o-nitroacetanilide much more soluble in acidic

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