Talk:Carbonate ester
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Ideas for expansion
[edit]- Alkylene carbonates
- Trimethylene carbonate
- Reactivity - transesterification, hydrolysis
- Non-bisphenol A polycarbonates & nucleophilic substitution of carbonate esters by diamines to give polyurethanes
- Bicarbonate esters
--Rifleman 82 (talk) 13:51, 3 August 2012 (UTC)
External links modified
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Oleochemical carbonates
[edit]I'm concerned about the Oleochemical carbonates section: it starts out talking about oleochemistry (i.e. getting the substituents from animal or plant sources) but it seems drift into a general discussion about long-chain substituents, which could in principle come from petrochemical sources. I don't know enough about the industry to be confident in fixing it, though. --Slashme (talk) 20:23, 21 November 2017 (UTC)
- Good catch. I read through Ullmann's on carbonate esters. That source mentions no fatty acid derivatives, so I conclude that they are unimportant and that some advocating editor inserted the section. --Smokefoot (talk) 23:30, 21 November 2017 (UTC)
Chemistry-jewelry connection?
[edit]Amusement for the day. For the image at right, Wiki commons recommended additional tags: "bead", "costume accessory", "jewellery", "necklace". The suggestion does illustrate the strong effect of the geminal dimethyl group on the conformation.--Smokefoot (talk) 16:24, 18 February 2020 (UTC)
![](http://upload.wikimedia.org/wikipedia/commons/thumb/4/4f/DINWOM10.png/244px-DINWOM10.png)
- Does the jewellery come Ingold? --Project Osprey (talk) 11:26, 19 February 2020 (UTC)
- Well the gem-dimethyl effect is striking. --Smokefoot (talk) 17:44, 19 February 2020 (UTC)
- These jokes would be funnier if we put more Thorpe into them. --Project Osprey (talk) 01:09, 20 February 2020 (UTC)
- Well the gem-dimethyl effect is striking. --Smokefoot (talk) 17:44, 19 February 2020 (UTC)