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  2. Nitrile - Wikipedia

    en.wikipedia.org/wiki/Nitrile

    The structure of a nitrile: the functional group is highlighted blue. In organic chemistry, a nitrile is any organic compound that has a −C≡N functional group.The name of the compound is composed of a base, which includes the carbon of the −C≡N, suffixed with "nitrile", so for example CH 3 CH 2 C≡N is called "propionitrile" (or propanenitrile). [1]

  3. 1,3-dipole - Wikipedia

    en.wikipedia.org/wiki/1,3-dipole

    Some oxides. Azoxide compounds (RN(O)NR) Carbonyl oxides (Criegee zwitterions) [4] [5] Nitrile oxides (RCN−O) Nitrous oxide (N 2 O) Nitrones (R 2 CN(R)O) Carbonyl oxide. Some imines: Azomethine imine; Nitrilimines (RCN−NR, analogous to nitrile oxide) Carbonyl imines; Some ylides. Azomethine ylide; Nitrile ylide (RCNCR' 2) Carbonyl ylide ...

  4. Nitric oxide - Wikipedia

    en.wikipedia.org/wiki/Nitric_oxide

    Nitric oxide (nitrogen oxide or nitrogen monoxide [1]) is a colorless gas with the formula NO. It is one of the principal oxides of nitrogen . Nitric oxide is a free radical : it has an unpaired electron , which is sometimes denoted by a dot in its chemical formula ( • N=O or • NO).

  5. Nitrogen compounds - Wikipedia

    en.wikipedia.org/wiki/Nitrogen_compounds

    One other possible oxide that has not yet been synthesised is oxatetrazole (N 4 O), an aromatic ring. [15] Nitrous oxide (N 2 O), better known as laughing gas, is made by thermal decomposition of molten ammonium nitrate at 250 °C. This is a redox reaction and thus nitric oxide and nitrogen are also produced as byproducts.

  6. Category:Nitrogen oxides - Wikipedia

    en.wikipedia.org/wiki/Category:Nitrogen_oxides

    This page was last edited on 1 December 2021, at 08:15 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  7. 1,3-Dipolar cycloaddition - Wikipedia

    en.wikipedia.org/wiki/1,3-Dipolar_cycloaddition

    However, a few examples exist of a stepwise mechanism for the catalyst-free 1,3-dipolar cycloaddition reactions of thiocarbonyl ylides, [6] and nitrile oxides [7] The generic mechanism of a 1,3-dipolar cycloaddition between a dipole and a dipolarophile to give a five-membered heterocycle, through a six-electron transition state.

  8. Nicotinonitrile - Wikipedia

    en.wikipedia.org/wiki/Nicotinonitrile

    The molecule consists of a pyridine ring with a nitrile group attached to the 3-position. A colorless solid, it is produced by ammoxidation of 3-methylpyridine: [2] H 3 CC 5 H 4 N + NH 3 + 1.5 O 2 → NCC 5 H 4 N + 3 H 2 O. Nicotinonitrile is a precursor to the vitamin niacin. [3]

  9. Nitrogen oxide - Wikipedia

    en.wikipedia.org/wiki/Nitrogen_oxide

    Due to relatively weak N–O bonding, all nitrogen oxides are unstable with respect to N 2 and O 2, which is the principle behind the catalytic converter, and prevents the oxygen and nitrogen in the atmosphere from combusting.