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A chemical equation is the symbolic representation of a chemical reaction in the form of symbols and chemical formulas.The reactant entities are given on the left-hand side and the product entities are on the right-hand side with a plus sign between the entities in both the reactants and the products, and an arrow that points towards the products to show the direction of the reaction. [1]
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Forming an ionic bond, Li and F become Li + and F − ions. An ion (/ ˈ aɪ. ɒ n,-ən /) [1] is an atom or molecule with a net electrical charge. The charge of an electron is considered to be negative by convention and this charge is equal and opposite to the charge of a proton, which is considered to be positive by convention. The net charge ...
They are present in total ionic equations to balance the charges of the ions. Whereas the Cu 2+ and CO 2− 3 ions combine to form a precipitate of solid CuCO 3. In reaction stoichiometry, spectator ions are removed from a complete ionic equation to form a net ionic equation. For the above example this yields:
with T A the total concentration of species A. Note that it is customary to omit the ionic charges when writing and using these equations. When the equilibrium constants are known and the total concentrations are specified there are two equations in two unknown "free concentrations" [A] and [H].
Complete ionic equations and net ionic equations are used to show dissociated ions in metathesis reactions. When performing calculations regarding the reacting of one or more aqueous solutions, in general one must know the concentration , or molarity , of the aqueous solutions.
Using the electroneutrality principle the assumption is made that the Co-N bond will have 50% ionic character thus resulting in a zero charge on the cobalt atom. Due to the difference in electronegativity the N-H bond would 17% ionic character and therefore a charge of 0.166 on each of the 18 hydrogen atoms.
In 1923, Peter Debye and Erich Hückel reported the first successful theory for the distribution of charges in ionic solutions. [7] The framework of linearized Debye–Hückel theory subsequently was applied to colloidal dispersions by S. Levine and G. P. Dube [8] [9] who found that charged colloidal particles should experience a strong medium-range repulsion and a weaker long-range attraction.