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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atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...
For example, in the formation of an ammonium ion from ammonia and hydrogen the ammonia molecule donates a pair of electrons to the proton; [11] the identity of the electrons is lost in the ammonium ion that is formed. Nevertheless, Lewis suggested that an electron-pair donor be classified as a base and an electron-pair acceptor be classified as ...
Other molecules have a tetrahedral arrangement of electron pairs around a central atom; for example ammonia (NH 3) with the nitrogen atom surrounded by three hydrogens and one lone pair. However the usual classification considers only the bonded atoms and not the lone pair, so that ammonia is actually considered as pyramidal. The H–N–H ...
Lone pairs (shown as pairs of dots) in the Lewis structure of hydroxide. In science, a lone pair refers to a pair of valence electrons that are not shared with another atom in a covalent bond [1] and is sometimes called an unshared pair or non-bonding pair. Lone pairs are found in the outermost electron shell of atoms.
A Lewis base or electron-pair donor is a molecule with one or more high-energy lone pairs of electrons which can be shared with a low-energy vacant orbital in an acceptor molecule to form an adduct. In addition to H + , possible electron-pair acceptors (Lewis acids) include neutral molecules such as BF 3 and high oxidation state metal ions such ...
The lone pair repels more strongly than bond pairs; therefore, the bond angle is not 109.5°, as expected for a regular tetrahedral arrangement, but 106.8°. [36] This shape gives the molecule a dipole moment and makes it polar. The molecule's polarity, and especially its ability to form hydrogen bonds, makes ammonia highly miscible with water ...
Ammonolysis reactions can be conducted with organic compounds to produce amines (molecules containing a nitrogen atom with a lone pair, :N), [2] or with inorganic compounds to produce nitrides. [3] [4] This reaction is analogous to hydrolysis in which water molecules are split.
In the case of water, with its 104.5° HOH angle, the OH bonding orbitals are constructed from O(~sp 4.0) orbitals (~20% s, ~80% p), while the lone pairs consist of O(~sp 2.3) orbitals (~30% s, ~70% p). As discussed in the justification above, the lone pairs behave as very electropositive substituents and have excess s character.