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Azanide is the IUPAC -sanctioned name for the anion NH− 2. The term is obscure; derivatives of NH− 2 are almost invariably referred to as amides, [1][2][3] despite the fact that amide also refers to the organic functional group – C (=O)−NR2. The anion NH− 2 is the conjugate base of ammonia, so it is formed by the self-ionization of ...
In chemistry, the amino radical, ·NH2, 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. In sufficiently high concentration, amino radicals dimerise to form hydrazine.
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atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...
Hydroxylamine (also known as hydroxyammonia) is an inorganic compound with the chemical formula N H 2 O H. The compound is in a form of a white hygroscopic crystals. [4] Hydroxylamine is almost always provided and used as an aqueous solution. It is consumed almost exclusively to produce Nylon-6.
Use. IUPAC nomenclature is used for the naming of chemical compounds, based on their chemical composition and their structure. [1] For example, one can deduce that 1-chloropropane has a Chlorine atom on the first carbon in the 3-carbon propane chain.
Imide. In organic chemistry, an imide is a functional group consisting of two acyl groups bound to nitrogen. [1] The compounds are structurally related to acid anhydrides, although imides are more resistant to hydrolysis. In terms of commercial applications, imides are best known as components of high-strength polymers, called polyimides.
In organic chemistry, an aromatic amine is an organic compound consisting of an aromatic ring attached to an amine. It is a broad class of compounds that encompasses anilines, but also many more complex aromatic rings and many amine substituents beyond NH2. Such compounds occur widely. [1] Representative aromatic amines. Aromatic ring.
The general structure of an imine. In organic chemistry, an imine (/ ɪˈmiːn / or / ˈɪmɪn /) is a functional group or organic compound containing a carbon – nitrogen double bond (C=N). The nitrogen atom can be attached to a hydrogen or an organic group (R). The carbon atom has two additional single bonds. [1][2] Imines are common in ...