Search results
Results From The WOW.Com Content Network
Instead, the slow step involves two molecules of NO 2. A possible mechanism for the overall reaction that explains the rate law is: 2 NO 2 → NO 3 + NO (slow) NO 3 + CO → NO 2 + CO 2 (fast) Each step is called an elementary step, and each has its own rate law and molecularity. The sum of the elementary steps gives the net reaction.
This page was last edited on 10 October 2008, at 02:16 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
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]
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:
Here k is the first-order rate constant, having dimension 1/time, [A](t) is the concentration at a time t and [A] 0 is the initial concentration. The rate of a first-order reaction depends only on the concentration and the properties of the involved substance, and the reaction itself can be described with a characteristic half-life. More than ...
Proteins purification and separation can be performed by precipitation in changing the nature of the solvent or the value of its relative permittivity (e.g., by replacing water by ethanol), or by increasing the ionic strength of the solution.
Dissociation in chemistry is a general process in which molecules (or ionic compounds such as salts, or complexes) separate or split into other things such as atoms, ions, or radicals, usually in a reversible manner.
They can be used to calculate mixed ion activity coefficients and water activities in solutions of high ionic strength for which the Debye–Hückel theory is no longer adequate. They are more rigorous than the equations of specific ion interaction theory (SIT theory), but Pitzer parameters are more difficult to determine experimentally than ...