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  2. Nitroethane - Wikipedia

    en.wikipedia.org/wiki/Nitroethane

    Nitroethane is an organic compound having the chemical formula C 2 H 5 NO 2. Similar in many regards to nitromethane , nitroethane is an oily liquid at standard temperature and pressure. Pure nitroethane is colorless and has a fruity odor.

  3. Nitro compound - Wikipedia

    en.wikipedia.org/wiki/Nitro_compound

    Free radical nitration of alkanes. [4] The reaction produces fragments from the parent alkane, creating a diverse mixture of products; for instance, nitromethane, nitroethane, 1-nitropropane, and 2-nitropropane are produced by treating propane with nitric acid in the gas phase (e.g. 350–450 °C and 8–12 atm).

  4. 1-Nitropropane - Wikipedia

    en.wikipedia.org/wiki/1-Nitropropane

    This reaction forms four nitroalkanes: nitromethane, nitroethane, 1-nitropropane, and 2-nitropropane. 1-nitropropane is also a byproduct of the process for making 2-nitropropane, which is done by vapour phase nitration of propane.

  5. Phenyl-2-nitropropene - Wikipedia

    en.wikipedia.org/wiki/Phenyl-2-nitropropene

    In the lab, phenyl-2-nitropropene is produced by the reaction of benzaldehyde and nitroethane in the presence of a basic catalyst like n-butylamine.The reaction is a nitroaldol reaction, and is a variant of a Knoevenagel condensation reaction, which is one of a broader class of reactions called Henry condensations, or simply Henry reactions.

  6. Nitroethylene - Wikipedia

    en.wikipedia.org/wiki/Nitroethylene

    The main use of nitroethylene is as an intermediate reagent in chemical synthesis. One example is the production of N-(2-nitroethyl)-aniline with aniline at room temperature. The reaction utilizes benzene as a solvent and proceeds to about 90% yield in 12 hours. [9] Reaction of nitroethylene and aniline

  7. Reduction of nitro compounds - Wikipedia

    en.wikipedia.org/wiki/Reduction_of_nitro_compounds

    Several methods have been described for the production of aryl hydroxylamines from aryl nitro compounds: Raney nickel and hydrazine at 0-10 °C [15] Electrolytic reduction [16] Zinc metal in aqueous ammonium chloride [17] Catalytic Rhodium on carbon with excess hydrazine monohydrate at room temperature [18]

  8. Nef reaction - Wikipedia

    en.wikipedia.org/wiki/Nef_reaction

    In organic chemistry, the Nef reaction is an organic reaction describing the acid hydrolysis of a salt of a primary or secondary nitroalkane (R−NO 2) to an aldehyde (R−CH=O) or a ketone (R 2 C=O) and nitrous oxide (N 2 O).

  9. Hexanitroethane - Wikipedia

    en.wikipedia.org/wiki/Hexanitroethane

    Hexanitroethane (HNE) is an organic compound with chemical formula C 2 N 6 O 12 or (O 2 N) 3 C-C(NO 2) 3.It is a solid matter with a melting point of 135 °C. Hexanitroethane is used in some pyrotechnic compositions as a nitrogen-rich oxidizer, e.g. in some decoy flare compositions and some propellants.