User talk:Alfa-ketosav/Archive1

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Please stop
Please stop renaming articles without first getting consensus. You can do so using the process outlined at WP:RM. Some of the new titles you are creating are inconsistent with Wikipedia naming conventions.

Also, you should not change the titles of journal articles in references to fit your preferred name as you did with this edit. Thank you. -- Ed (Edgar181) 14:35, 2 May 2018 (UTC)
 * But we use benzenehexol trisoxalate, not hexahydroxybenzene trisoxalate. Alfa-ketosav (talk) 14:39, 2 May 2018 (UTC)
 * The reference in the article is titled "A new carbon oxide synthesis of hexahydroxybenzene tris oxalate" (well it did until you inappropriately altered the reference), so it could be argued that way as well. This is the reason that such changes to Wikipedia page titles should be discussed first.  -- Ed (Edgar181) 14:43, 2 May 2018 (UTC)
 * The preferred name is benzene-1,2,3,4,5,6-hexol, not 1,2,3,4,5,6-hexahydroxybenzene. Alfa-ketosav (talk) 14:53, 2 May 2018 (UTC)
 * Well obviously it's not preferred by at least one research group who has published on the topic. Wikipedia chemistry articles are not necessarily titled using any specific system of chemical nomenclature, such as IUPAC names.  Guidelines are described at Naming conventions (chemistry).  This is why getting consensus is important before making a move.  -- Ed (Edgar181) 15:06, 2 May 2018 (UTC)
 * I agree with Edgar181, and hence I have reverted your moves and your alterations of reference titles. If you would like these articles to be renamed, please discuss it on the talk pages or at Wikipedia talk:WikiProject Chemicals and do it only if and after you get consensus for it. Double sharp (talk) 10:55, 3 May 2018 (UTC)

Butalene
The butalene is indeed aromatic as shown by quantum chemical calculations. But both SMILES forms (c1ccc21cc2 and C=1C=C2C=CC=12) are equally correct and valid (the same as 2 SMILES's for benzene - c1ccccc1 and C=1C=CC=CC=1). I changed the form to non-aromatic because the Wikipedia Chemical Structure Explorer http://www.cheminfo.org/wikipedia/ is not able to process the aromatic form (what is apparently a bug in the SMILES parser of this tool). After your reversal I added now the non-aromatic form as an alternative SMILES, so also this molecules can be added to the database. SMILESmaster (talk) 13:18, 3 November 2018 (UTC)

File:Dirubídium.png listed for discussion
A file that you uploaded or altered, File:Dirubídium.png, has been listed at Files for discussion. Please see the to see why it has been listed (you may have to search for the title of the image to find its entry). Feel free to add your opinion on the matter below the nomination. Thank you. DMacks (talk) 04:56, 26 December 2019 (UTC)