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The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
A metal ion in aqueous solution or aqua ion is a cation, dissolved in water, of chemical formula [M(H 2 O) n] z+.The solvation number, n, determined by a variety of experimental methods is 4 for Li + and Be 2+ and 6 for most elements in periods 3 and 4 of the periodic table.
The nitronium ion, [N O 2] +, is a cation.It is an onium ion because its nitrogen atom has +1 charge, similar to ammonium ion [NH 4] +.It is created by the removal of an electron from the paramagnetic nitrogen dioxide molecule NO 2, or the protonation of nitric acid HNO 3 (with removal of H 2 O).
Quaternary ammonium cations have four organic groups attached to the nitrogen atom, they lack a hydrogen atom bonded to the nitrogen atom. These cations, such as the tetra-n-butylammonium cation, are sometimes used to replace sodium or potassium ions to increase the solubility of the associated anion in organic solvents.
Ionic radius, r ion, is the radius of a monatomic ion in an ionic crystal structure. Although neither atoms nor ions have sharp boundaries, they are treated as if they were hard spheres with radii such that the sum of ionic radii of the cation and anion gives the distance between the ions in a crystal lattice.
In the simplest case, the cation is a metal atom and the anion is a nonmetal atom, but these ions can be more complex, e.g. polyatomic ions like NH + 4 or SO 2− 4. In simpler words, an ionic bond results from the transfer of electrons from a metal to a non-metal to obtain a full valence shell for both atoms.
An example is the ammonium cation of 8 valence electrons (5 from nitrogen, 4 from hydrogens, minus 1 electron for the cation's positive charge): Drawing Lewis structures with electron pairs as dashes emphasizes the essential equivalence of bond pairs and lone pairs when counting electrons and moving bonds onto atoms.
Some of the first studies on the cation–π interaction involved looking at the interactions of charged, nitrogenous molecules in cyclophane host–guest chemistry. It was found that even when anionic solubilizing groups were appended to aromatic host capsules, cationic guests preferred to associate with the π-system in many cases.