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  2. Nitroaniline - Wikipedia

    en.wikipedia.org/wiki/Nitroaniline

    The term nitroaniline in chemistry refers to a derivative of aniline (C 6 H 5 NH 2) containing a nitro group (—NO 2) There are three simple nitroanilines of formula C 6 H 4 (NH 2)(NO 2) which differ only in the position of the nitro group: 2-Nitroaniline; 3-Nitroaniline; 4-Nitroaniline

  3. Sphygmomanometer - Wikipedia

    en.wikipedia.org/wiki/Sphygmomanometer

    A sphygmomanometer (/ ˌ s f ɪ ɡ m oʊ m ə ˈ n ɒ m ɪ t ə r / SFIG-moh-mə-NO-mi-tər), also known as a blood pressure monitor, or blood pressure gauge, is a device used to measure blood pressure, composed of an inflatable cuff to collapse and then release the artery under the cuff in a controlled manner, [1] and a mercury or aneroid manometer to measure the pressure.

  4. 4-Nitroaniline - Wikipedia

    en.wikipedia.org/wiki/4-Nitroaniline

    4-Nitroaniline, p-nitroaniline or 1-amino-4-nitrobenzene is an organic compound with the formula C 6 H 6 N 2 O 2. A yellow solid, it is one of three isomers of nitroaniline. It is an intermediate in the production of dyes, antioxidants, pharmaceuticals, gasoline, gum inhibitors, poultry medicines, and as a corrosion inhibitor. [3]

  5. 4-Nitrochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/4-nitrochlorobenzene

    4-Nitrochlorobenzene is the organic compound with the formula ClC 6 H 4 NO 2. It is a pale yellow solid. 4-Nitrochlorobenzene is a common intermediate in the production of a number of industrially useful compounds, including antioxidants commonly found in rubber. Other isomers with the formula ClC 6 H 4 NO 2 include 2-nitrochlorobenzene and 3 ...

  6. 2,6-Dichloro-4-nitroaniline - Wikipedia

    en.wikipedia.org/wiki/2,6-Dichloro-4-nitroaniline

    2,6-Dichloro-4-nitroaniline is an organic compound with the formula O 2 NC 6 H 2 Cl 2 NH 2. It is the most widely discussed isomer of dichloronitroaniline, mainly as a precursor to the azo dye disperse brown 1. It is prepared by treatment of 4-nitroaniline with a mixture of hydrochloric acid and hydrogen peroxide (a source of chlorine). [3] [4]

  7. C6H4Cl2N2O2 - Wikipedia

    en.wikipedia.org/wiki/C6H4Cl2N2O2

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  8. o-Phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/O-Phenylenediamine

    Commonly, 2-nitrochlorobenzene is treated with ammonia to generate 2-nitroaniline, whose nitro group is then reduced: [4] ClC 6 H 4 NO 2 + 2 NH 3 → H 2 NC 6 H 4 NO 2 + NH 4 Cl H 2 NC 6 H 4 NO 2 + 3 H 2 → H 2 NC 6 H 4 NH 2 + 2 H 2 O. In the laboratory, the reduction of the nitroaniline is effected with zinc powder in ethanol, followed by ...

  9. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 1 ⁄ 2 O 2 → ClCH 2 CH 2 Cl + H 2 O. Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.

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