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Preparing p-nitroacetanilide is significant for its application in organic synthesis and as an intermediate in the production of dyes and pharmaceuticals. The reaction involves the nitration of acetanilide, which introduces a nitro group at the para position, enhancing the compound's reactivity. This synthesis serves as an important example of electrophilic aromatic substitution, illustrating key concepts in organic chemistry. Additionally, p-nitroacetanilide can be used to study reaction mechanisms and the effects of substituents on aromatic systems.

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2mo ago

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