Template talk:Acetates

There is an error: Ac means acetyl CH3C(=O)- So if someone wants to write copper acetate he should write: Cu(OAc)2 not CuAc2 Acetic acid is: AcOH not AcH --Synthesium (talk) 12:59, 23 September 2015 (UTC)[reply]__DTELLIPSISBUTTON__{"threadItem":{"timestamp":"2015-09-23T12:59:00.000Z","author":"Synthesium","type":"comment","level":1,"id":"c-Synthesium-2015-09-23T12:59:00.000Z","replies":["c-Graeme_Bartlett-2015-09-24T00:05:00.000Z-Synthesium-2015-09-23T12:59:00.000Z"]}}-->

Thanks, I have changed things. Graeme Bartlett (talk) 00:05, 24 September 2015 (UTC)[reply]__DTELLIPSISBUTTON__{"threadItem":{"timestamp":"2015-09-24T00:05:00.000Z","author":"Graeme Bartlett","type":"comment","level":2,"id":"c-Graeme_Bartlett-2015-09-24T00:05:00.000Z-Synthesium-2015-09-23T12:59:00.000Z","replies":[]}}-->
__DTSUBSCRIBEBUTTONDESKTOP__{"headingLevel":2,"name":"h-Mithoron-2018-04-04T23:25:00.000Z","type":"heading","level":0,"id":"h-Salts_and_ester?_What_about_halides?-2018-04-04T23:25:00.000Z","replies":["c-Mithoron-2018-04-04T23:25:00.000Z-Salts_and_ester?_What_about_halides?"],"text":"Salts and ester? What about halides?","linkableTitle":"Salts and ester? What about halides?"}-->

Salts and ester? What about halides?

__DTELLIPSISBUTTON__{"threadItem":{"headingLevel":2,"name":"h-Mithoron-2018-04-04T23:25:00.000Z","type":"heading","level":0,"id":"h-Salts_and_ester?_What_about_halides?-2018-04-04T23:25:00.000Z","replies":["c-Mithoron-2018-04-04T23:25:00.000Z-Salts_and_ester?_What_about_halides?"]}}-->
__DTSUBSCRIBEBUTTONMOBILE__{"headingLevel":2,"name":"h-Mithoron-2018-04-04T23:25:00.000Z","type":"heading","level":0,"id":"h-Salts_and_ester?_What_about_halides?-2018-04-04T23:25:00.000Z","replies":["c-Mithoron-2018-04-04T23:25:00.000Z-Salts_and_ester?_What_about_halides?"],"text":"Salts and ester? What about halides?","linkableTitle":"Salts and ester? What about halides?"}-->

Description is pretty bad, CH3COX where x=I,Br,Cl,F,Ac,B aren't salts or esters. Also AcOAc isn't in proper place, should be rather under ester as carbon not O is bound to acetate oxygen. Under "O" there could be peroxacetic acid and it's derivatives. Mithoron (talk) 23:25, 4 April 2018 (UTC)[reply]__DTELLIPSISBUTTON__{"threadItem":{"timestamp":"2018-04-04T23:25:00.000Z","author":"Mithoron","type":"comment","level":1,"id":"c-Mithoron-2018-04-04T23:25:00.000Z-Salts_and_ester?_What_about_halides?","replies":["c-Graeme_Bartlett-2018-04-05T00:06:00.000Z-Mithoron-2018-04-04T23:25:00.000Z"]}}-->

I have moved things around as you suggest. And there is not even an article on "acetyl ester" so I have stopped drawing attention to it. Graeme Bartlett (talk) 00:06, 5 April 2018 (UTC)[reply]__DTELLIPSISBUTTON__{"threadItem":{"timestamp":"2018-04-05T00:06:00.000Z","author":"Graeme Bartlett","type":"comment","level":2,"id":"c-Graeme_Bartlett-2018-04-05T00:06:00.000Z-Mithoron-2018-04-04T23:25:00.000Z","replies":[]}}-->