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  2. 1-Nitropropane - Wikipedia

    en.wikipedia.org/wiki/1-Nitropropane

    1-nitropropane is produced industrially by the reaction of propane and nitric acid. 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.

  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. Nitroethane - Wikipedia

    en.wikipedia.org/wiki/Nitroethane

    This exothermic reaction produces four industrially significant nitroalkanes: nitromethane, nitroethane, 1-nitropropane, and 2-nitropropane. The reaction involves free radicals, such as CH 3 CH 2 CH 2 O., which arise via homolysis of the corresponding nitrite ester. These alkoxy radicals are susceptible to C—C fragmentation reactions, which ...

  5. Nitropropane - Wikipedia

    en.wikipedia.org/wiki/Nitropropane

    Nitropropane may refer to: 1-Nitropropane; 2-Nitropropane This page was last edited on 16 May 2022, at 02:06 (UTC). Text is available under the Creative Commons ...

  6. 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). The reaction has been the subject of several literature reviews. [1] [2] [3] The Nef reaction: 1. Salt of a nitroalkane ...

  7. 1,4-Dioxane - Wikipedia

    en.wikipedia.org/wiki/1,4-Dioxane

    1,4-Dioxane (/ d aɪ ˈ ɒ k s eɪ n /) is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether . The compound is often called simply dioxane because the other dioxane isomers ( 1,2- and 1,3- ) are rarely encountered.

  8. C3H7NO2 - Wikipedia

    en.wikipedia.org/wiki/C3H7NO2

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  9. 1,2-Dioxolane - Wikipedia

    en.wikipedia.org/wiki/1,2-Dioxolane

    Synthesis methods for the 1,2-dioxolane core structure include oxidation of cyclopropane derivatives with singlet oxygen [3] or molecular oxygen with a suitable catalyst, [4] [5] the use of autooxidation, nucleophilic displacement with hydrogen peroxide, treatment with mercury(II) nitrate, photolysis of extended π-systems, [6] reaction of a bis-silylperoxide and an alkene, [7] or reaction ...