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Meta-nitroaniline

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Organic Chemistry

Definition

meta-Nitroaniline is an organic compound with the chemical formula C₆H₆N₂O₂. It is a derivative of aniline with a nitro group (-NO₂) substituted at the meta position on the benzene ring. This structural feature makes meta-nitroaniline an important intermediate in the synthesis of various dyes, pharmaceuticals, and other organic compounds.

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5 Must Know Facts For Your Next Test

  1. meta-Nitroaniline is a yellow crystalline solid that is moderately soluble in water and organic solvents.
  2. The nitro group in meta-nitroaniline is a strong electron-withdrawing substituent, which affects the reactivity and properties of the compound.
  3. meta-Nitroaniline is an important intermediate in the synthesis of various dyes, such as azo dyes and disperse dyes, as well as in the production of certain pharmaceuticals.
  4. The meta-substitution pattern of the nitro group in meta-nitroaniline affects the reactivity and selectivity of subsequent reactions, compared to ortho- or para-substituted nitroanilines.
  5. meta-Nitroaniline can undergo various organic reactions, including electrophilic aromatic substitution, nucleophilic aromatic substitution, and reduction of the nitro group to an amino group.

Review Questions

  • Explain the significance of the meta-substitution pattern in meta-nitroaniline and how it affects the reactivity of the compound.
    • The meta-substitution pattern of the nitro group in meta-nitroaniline is important because it affects the reactivity and selectivity of subsequent reactions. The nitro group is a strong electron-withdrawing substituent, and its position at the meta position on the benzene ring influences the distribution of electron density within the molecule. This, in turn, impacts the reactivity and the types of reactions that meta-nitroaniline can undergo, often leading to different products compared to ortho- or para-substituted nitroanilines.
  • Describe the role of meta-nitroaniline as an important intermediate in the synthesis of various organic compounds, such as dyes and pharmaceuticals.
    • meta-Nitroaniline is a versatile and important intermediate in organic synthesis. Its unique structural features, particularly the meta-substitution pattern of the nitro group, make it a valuable precursor for the production of a wide range of dyes, including azo dyes and disperse dyes. Additionally, meta-nitroaniline is used in the synthesis of certain pharmaceuticals, where its reactivity and selectivity are exploited to create desired molecular structures. The ability to further functionalize meta-nitroaniline through various organic reactions is a key reason for its importance as an intermediate in the chemical industry.
  • Analyze the potential reaction pathways and products that can be obtained from meta-nitroaniline, considering its reactivity and the influence of the meta-substitution pattern.
    • Given the meta-substitution pattern and the presence of both the nitro group and the amino group, meta-nitroaniline can undergo a variety of organic reactions. These include electrophilic aromatic substitution, where the meta-substitution pattern affects the regioselectivity of the reaction; nucleophilic aromatic substitution, where the nitro group can be displaced; and reduction of the nitro group to an amino group, which opens up further synthetic possibilities. The unique reactivity of meta-nitroaniline, stemming from the interplay between the substituents and their positions on the benzene ring, allows for the synthesis of a diverse range of organic compounds with varied applications in the fields of dyes, pharmaceuticals, and other industries.

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