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Systematic oxidation state is chosen from close alternatives as a pedagogical description. An example is the oxidation state of phosphorus in H 3 PO 3 (structurally diprotic HPO(OH) 2) taken nominally as +3, while Allen electronegativities of phosphorus and hydrogen suggest +5 by a narrow margin that makes the two alternatives almost equivalent:
The oxidation states are also maintained in articles of the elements (of course), and systematically in the table {{Infobox element/symbol-to-oxidation-state}}
Latimer diagrams can be used in the construction of Frost diagrams, as a concise summary of the standard electrode potentials relative to the element.Since Δ r G o = -nFE o, the electrode potential is a representation of the Gibbs energy change for the given reduction.
The oxidation states are also maintained in articles of the elements (of course), and systematically in the table {{Infobox element/symbol-to-oxidation-state}}
In aqueous solutions, redox potential is a measure of the tendency of the solution to either gain or lose electrons in a reaction. A solution with a higher (more positive) reduction potential than some other molecule will have a tendency to gain electrons from this molecule (i.e. to be reduced by oxidizing this other molecule) and a solution with a lower (more negative) reduction potential ...
Chloride can be oxidized but not reduced. The first oxidation, as employed in the chlor-alkali process, is conversion to chlorine gas. Chlorine can be further oxidized to other oxides and oxyanions including hypochlorite (ClO −, the active ingredient in chlorine bleach), chlorine dioxide (ClO 2), chlorate (ClO − 3), and perchlorate (ClO − 4).
As another difference, chlorine has a significant chemistry in positive oxidation states while fluorine does not. Chlorination often leads to higher oxidation states than bromination or iodination but lower oxidation states than fluorination. Chlorine tends to react with compounds including M–M, M–H, or M–C bonds to form M–Cl bonds. [40]
The chemical state of a group of elements, can be similar to, but not identical to, the chemical state of another similar group of elements because the two groups have different ratios of the same elements and exhibit different chemical, electronic, and physical properties that can be detected by various spectroscopic techniques.