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  2. Reduction of nitro compounds - Wikipedia

    en.wikipedia.org/wiki/Reduction_of_nitro_compounds

    The reduction of nitro compounds are chemical reactions of wide interest in organic chemistry. The conversion can be effected by many reagents. The nitro group was one of the first functional groups to be reduced. Alkyl and aryl nitro compounds behave differently. Most useful is the reduction of aryl nitro compounds.

  3. Denitrification - Wikipedia

    en.wikipedia.org/wiki/Denitrification

    Direct reduction from nitrate to ammonium, a process known as dissimilatory nitrate reduction to ammonium or DNRA, [6] is also possible for organisms that have the nrf-gene. [ 7 ] [ 8 ] This is less common than denitrification in most ecosystems as a means of nitrate reduction.

  4. Béchamp reduction - Wikipedia

    en.wikipedia.org/wiki/Béchamp_reduction

    The Béchamp reduction (or Béchamp process) is a chemical reaction that converts aromatic nitro compounds to their corresponding anilines using iron as the reductant: [1] 4 C 6 H 5 NO 2 + 9 Fe + 4 H 2 O → 4 C 6 H 5 NH 2 + 3 Fe 3 O 4. This reaction was once a major route to aniline, but catalytic hydrogenation is the preferred method. [2]

  5. Quench polish quench - Wikipedia

    en.wikipedia.org/wiki/Quench_polish_quench

    Field immersion comparison chart ASTM B117 Salt Spray Test The chart on the right shows a comparison of corrosion resistance against other surface treatments, based on field immersion tests. Test conditions for the immersion test are full immersion in 3% sodium chloride plus 3 g / L of hydrogen peroxide for 24 hours.

  6. Nitro compound - Wikipedia

    en.wikipedia.org/wiki/Nitro_compound

    The structure of an organic nitro compound. In organic chemistry, nitro compounds are organic compounds that contain one or more nitro functional groups (−NO 2). The nitro group is one of the most common explosophores (functional group that makes a compound explosive) used globally. The nitro group is also strongly electron-withdrawing.

  7. Zinin reaction - Wikipedia

    en.wikipedia.org/wiki/Zinin_reaction

    Zinin reaction or Zinin reduction involves reduction of nitro aromatic compounds to the amines using sodium sulfide. [1] It is used to convert nitrobenzenes to anilines. [2] [3] The reaction selectively reduces nitro groups in the presence of other easily reduced functional groups (e.g., aryl halides and C=C bonds) are present in the molecule.

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    mail.aol.com

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  9. Table of standard reduction potentials for half-reactions ...

    en.wikipedia.org/wiki/Table_of_standard...

    ′, an apparent formal standard reduction potential at pH 7 in given conditions and also depending on the ratio =. This requires thus to dispose of a clear definition of the considered reduction potential, and of a sufficiently detailed description of the conditions in which it is valid, along with a complete expression of the corresponding ...