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  2. Cyclohexylamine - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylamine

    3D model Interactive image ... It has a fishy odor and is miscible with water. Like other amines, it is a weak base, ... C 6 H 5 NH 2 + 3 H 2 → C 6 H 11 NH 2.

  3. Hexylamine - Wikipedia

    en.wikipedia.org/wiki/Hexylamine

    Hexylamine or n-hexylamine is a chemical compound with the formula CH 3 CH 2 CH 2 CH 2 CH 2 CH 2 NH 2. This colorless liquid is one of the isomeric amines of hexane. At standard temperature and pressure, it has the ammonia/bleach odor common to amines and is soluble in almost all organic solvents.

  4. Chemosynthesis - Wikipedia

    en.wikipedia.org/wiki/Chemosynthesis

    Venenivibrio stagnispumantis gains energy by oxidizing hydrogen gas.. In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules (usually carbon dioxide or methane) and nutrients into organic matter using the oxidation of inorganic compounds (e.g., hydrogen gas, hydrogen sulfide) or ferrous ions as a source of energy, rather than sunlight, as in ...

  5. Methylhexanamine - Wikipedia

    en.wikipedia.org/wiki/Methylhexanamine

    Methylhexanamine (also known as methylhexamine, 1,3-dimethylamylamine, 1,3-DMAA, dimethylamylamine, and DMAA; trade names Forthane and Geranamine) is an indirect sympathomimetic drug invented and developed by Eli Lilly and Company and marketed as an inhaled nasal decongestant from 1948 until it was voluntarily withdrawn from the market in the 1980s.

  6. Thermochemical cycle - Wikipedia

    en.wikipedia.org/wiki/Thermochemical_cycle

    During the reduction half-cycle of the stochiometric cycle, the metal oxide is reduced and forms a new metal oxide with different oxidation states (Fe 3 O 4 → 3FeO + 1/2 O 2); a non-stochiometric cycle's reduction of the metal oxide will produce vacancies, often oxygen vacancies, but the crystal structure remains stable and only a portion of ...

  7. 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.

  8. A ‘good ‘ol American boy’ and a woman everyone loved. Days after the murder, the Sarasota Herald-Tribune interviewed Greg’s co-workers at the South Florida Sod Farm.

  9. Ammonium hexachloroplatinate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_hexachloroplatinate

    Ammonium hexachloroplatinate, also known as ammonium chloroplatinate, is the inorganic compound with the formula (NH 4) 2 [PtCl 6]. It is a rare example of a soluble platinum(IV) salt that is not hygroscopic. It forms intensely yellow solutions in water. In the presence of 1M NH 4 Cl, its solubility is only 0.0028 g/100 mL.