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Oxidation state was nominated as a Natural sciences good article, but it did not meet the good article criteria at the time (April 26, 2021). There are suggestions on the review page for improving the article. If you can improve it, please do; it may then be renominated. |
The contents of the Oxidation number page were merged into Oxidation state on 18:04, 1 July 2013. For the contribution history and old versions of the redirected page, please see its history; for the discussion at that location, see its talk page. |
The contents of the List of oxidation states of the elements page were merged into Oxidation state on 14:54, 22 March 2019 (UTC). For the contribution history and old versions of the redirected page, please see its history; for the discussion at that location, see its talk page. |
Text and/or other creative content from List of oxidation states of the elements was copied or moved into Oxidation state. The former page's history now serves to provide attribution for that content in the latter page, and it must not be deleted as long as the latter page exists. |
I have added a correction to redox equation 1 which was pointed out by DIRAC66 in 2017 but which I missed until nowMcardlep (talk) 08:28, 24 May 2019 (UTC)
I see that in the article copernicium 0 charge is counted as an observed oxidation state, bold because it is a main one. This is not included in whatever the file that looks like File:Langmuir valence.png|700px with all the oxidation states is. Is this accurate, and if it is, how should it be added? --Ammonium121 (talk) 18:40, 22 April 2021 (UTC)
"Several criteria were considered for the ionic approximation:
Point b may be deceptive: in CO the negative end of the dipole is C; in pyrrole the dipole vector points from N to a direction in the middle of the ring. Patrizio 93.147.230.142 (talk) 16:28, 8 January 2023 (UTC)
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