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  2. Amino radical - Wikipedia

    en.wikipedia.org/wiki/Amino_radical

    In chemistry, the amino radical, ·NH 2, also known as the aminyl or azanyl, is the neutral form of the amide ion (NH − 2).Aminyl radicals are highly reactive and consequently short-lived, like most radicals; however, they form an important part of nitrogen chemistry.

  3. Aniline - Wikipedia

    en.wikipedia.org/wiki/Aniline

    The lone electron pair on the nitrogen delocalizes into the pi system of the benzene ring. This is responsible for nitrogen's weaker basicity compared to other amines. Missing in such an analysis is consideration of solvation. Aniline is, for example, more basic than ammonia in the gas phase, but ten thousand times less so in aqueous solution. [21]

  4. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3 (in which the bond angle between the nitrogen and hydrogen is 107°), wherein one or more hydrogen atoms have been replaced by a substituent such as an ...

  5. NH2 - Wikipedia

    en.wikipedia.org/wiki/NH2

    NH2 or similar may refer to: Azanide (chemical formula NH − 2) Amino radical (chemical formula NH • 2) Nitrenium ion (chemical formula NH + 2) Primary amide group (chemical formula -NH 2) National Harbor–Alexandria Line (Route NH2), a WMATA bus line between Alexandria, Virginia and Prince George's County, Maryland; National Highway 2 (India)

  6. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is a natural constituent of petroleum and is one of the elementary petrochemicals. Due to the cyclic continuous pi bonds between the carbon atoms, benzene is classed as an aromatic hydrocarbon. Benzene is a colorless and highly flammable liquid with a sweet smell, and is partially responsible for the aroma of gasoline.

  7. Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Mannich_reaction

    In organic chemistry, the Mannich reaction is a three-component organic reaction that involves the amino alkylation of an acidic proton next to a carbonyl (C=O) functional group by formaldehyde (H−CHO) and a primary or secondary amine (−NH 2) or ammonia (NH 3). [1]

  8. Benzylamine - Wikipedia

    en.wikipedia.org/wiki/Benzylamine

    Benzylamine, also known as phenylmethylamine, is an organic chemical compound with the condensed structural formula C 6 H 5 CH 2 NH 2 (sometimes abbreviated as PhCH 2 NH 2 or BnNH 2).It consists of a benzyl group, C 6 H 5 CH 2, attached to an amine functional group, NH 2.

  9. Ammonolysis - Wikipedia

    en.wikipedia.org/wiki/Ammonolysis

    Ammonolysis can be used to synthesize nitrides (and oxynitrides) by reacting various metal precursors with ammonia, some options include chemical vapor deposition, [3] treating metals or metal oxides with ammonia gas, [15] or liquid supercritical ammonia (also known as "ammonothermal" synthesis, analogous to hydrothermal synthesis).