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Formal charges in ozone and the nitrate anion. In chemistry, a formal charge (F.C. or q*), in the covalent view of chemical bonding, is the hypothetical charge assigned to an atom in a molecule, assuming that electrons in all chemical bonds are shared equally between atoms, regardless of relative electronegativity.
The nitrate ion carries a formal charge of −1. [citation needed] This charge results from a combination formal charge in which each of the three oxygens carries a − 2 ⁄ 3 charge, [citation needed] whereas the nitrogen carries a +1 charge, all these adding up to formal charge of the polyatomic nitrate ion.
In terms of Lewis structures, formal charge is used in the description, comparison, and assessment of likely topological and resonance structures [7] by determining the apparent electronic charge of each atom within, based upon its electron dot structure, assuming exclusive covalency or non-polar bonding.
Nitrite is an ambidentate ligand and can form a wide variety of coordination complexes by binding to metal ions in several ways. [2] Two examples are the red nitrito complex [Co(NH 3 ) 5 (ONO)] 2+ is metastable , isomerizing to the yellow nitro complex [Co(NH 3 ) 5 (NO 2 )] 2+ .
As an example, summing bond orders in the ammonium cation yields −4 at the nitrogen of formal charge +1, with the two numbers adding to the oxidation state of −3: The sum of oxidation states in the ion equals its charge (as it equals zero for a neutral molecule). Also in anions, the formal (ionic) charges have to be considered when nonzero.
There are two possible structures for hydrogen cyanide, HCN and CNH, differing only as to the position of the hydrogen atom. The structure with hydrogen attached to nitrogen, CNH, leads to formal charges of -1 on carbon and +1 on nitrogen, which would be partially compensated for by the electronegativity of nitrogen and Pauling calculated the net charges on H, N and C as -0.79, +0.75 and +0.04 ...
The electronic structure of a coordination complex can be described in terms of the set of ligands each donating a pair of electrons to a metal centre. For example, in hexamminecobalt(III) chloride, each ammonia ligand donates its lone pair of electrons to the cobalt(III) ion. In this case, the bonds formed are described as coordinate bonds.
N 2 O 4 undergoes molecular autoionization to give [NO +] [NO 3 −], with the former nitrosonium ion being a strong oxidant. The method is illustrated by the route to β-Cu(NO 3) 2: Cu + 2 N 2 O 4 → Cu(NO 3) 2 + 2 NO. Many metals, metal halides, and metal carbonyls undergo similar reactions, but the product formulas can be deceptive.