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Lone pairs in ammonia (A), water (B), and hydrogen chloride (C) A single lone pair can be found with atoms in the nitrogen group, such as nitrogen in ammonia. Two lone pairs can be found with atoms in the chalcogen group, such as oxygen in water. The halogens can carry three lone pairs, such as in hydrogen chloride.
A carbon–nitrogen bond is a covalent bond between carbon and nitrogen and is one of the most abundant bonds in organic chemistry and biochemistry. [1]Nitrogen has five valence electrons and in simple amines it is trivalent, with the two remaining electrons forming a lone pair.
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. The ...
These complexes, in which a nitrogen molecule donates at least one lone pair of electrons to a central metal cation, illustrate how N 2 might bind to the metal(s) in nitrogenase and the catalyst for the Haber process: these processes involving dinitrogen activation are vitally important in biology and in the production of fertilisers. [1] [2]
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(NH 3 (in which the bond angle between the nitrogen and hydrogen is 170°), wherein one or more hydrogen atoms have been replaced by a substituent such as an ...
The structural differences, distinct reactivity, and increased stability of the unsaturated ring is attributed the olefinic C=C bond which creates a 6π aromatic ring with the two nitrogen lone pairs. The Si-N bond length discrepancy mentioned above is a strong indication of π delocalization.
Nitrogen forms an extensive series of nitrides with carbon, including those with chain-, graphitic-, and fullerenic-like structures. [29] It resembles oxygen with its high electronegativity and concomitant capability for hydrogen bonding and the ability to form coordination complexes by donating its lone pairs of electrons.
In non-basic aromatic rings the lone pair of electrons of the nitrogen atom is delocalized and contributes to the aromatic pi electron system. In these compounds the nitrogen atom is connected to a hydrogen atom. Examples of non-basic nitrogen-containing aromatic rings are pyrrole and indole. Pyrrole contains a lone pair that is part of the pi ...