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  2. Haber process - Wikipedia

    en.wikipedia.org/wiki/Haber_process

    Nitrogen gas (N 2) is unreactive because the atoms are held together by triple bonds. The Haber process relies on catalysts that accelerate the scission of these bonds. Two opposing considerations are relevant: the equilibrium position and the reaction rate. At room temperature, the equilibrium is in favor of ammonia, but the reaction does not ...

  3. Nitrogen compounds - Wikipedia

    en.wikipedia.org/wiki/Nitrogen_compounds

    Top diagram shows potentials at pH 0; bottom diagram shows potentials at pH 14. [5] Industrially, ammonia (NH 3) is the most important compound of nitrogen and is prepared in larger amounts than any other compound, because it contributes significantly to the nutritional needs of terrestrial organisms by serving as a precursor to food and ...

  4. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. . Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou

  5. Hydrogen compounds - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_compounds

    Water molecules have two hydrogen atoms and one oxygen atom. While H 2 is not very reactive under standard conditions, it does form compounds with most elements. Hydrogen can form compounds with elements that are more electronegative, such as halogens (F, Cl, Br, I), or oxygen; in these compounds hydrogen takes on a partial positive charge. [1]

  6. Pyramidal inversion - Wikipedia

    en.wikipedia.org/wiki/Pyramidal_inversion

    Pyramidal inversion in nitrogen and amines is known as nitrogen inversion. [8] It is a rapid oscillation of the nitrogen atom and substituents, the nitrogen "moving" through the plane formed by the substituents (although the substituents also move - in the other direction); [ 9 ] the molecule passing through a planar transition state . [ 10 ]

  7. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    The nitrogen atom has only 6 electrons assigned to it. One of the lone pairs on an oxygen atom must form a double bond, but either atom will work equally well. Therefore, there is a resonance structure. Tie up loose ends. Two Lewis structures must be drawn: Each structure has one of the two oxygen atoms double-bonded to the nitrogen atom.

  8. Germanium(II) hydrides - Wikipedia

    en.wikipedia.org/wiki/Germanium(II)_Hydrides

    The reaction progresses by the end-on insertion of the diazoalkane into the Ge(II)-H bond, with subsequent hydrogen transfer to the nitrogen. Electronic structure analysis shows that the stability of the product stems from a shifting of electron density from the N-N bond onto the Ge-N bond. The analysis also shows that diazoalkane insertion ...

  9. 2-Pyridone - Wikipedia

    en.wikipedia.org/wiki/2-Pyridone

    The amide group can be involved in hydrogen bonding to other nitrogen- and oxygen-containing species.. The predominant solid state form is 2-pyridone. This has been confirmed by X-ray crystallography which shows that the hydrogen in solid state is closer to the nitrogen than to the oxygen (because of the low electron density at the hydrogen the exact positioning is difficult), and IR ...