Timeline for Determine compound acidity based on structure
Current License: CC BY-SA 3.0
7 events
| when toggle format | what | by | license | comment | |
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| Nov 27, 2017 at 18:03 | history | edited | xavier_fakerat |
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| Jan 6, 2014 at 11:30 | vote | accept | atmosx | ||
| Jan 6, 2014 at 10:42 | answer | added | Klaus-Dieter Warzecha | timeline score: 2 | |
| Jan 5, 2014 at 20:03 | history | tweeted | twitter.com/#!/StackChemistry/status/419922155552661504 | ||
| Jan 5, 2014 at 15:28 | comment | added | G M | Welcome! I think you can find some information in this question. In organic chemistry you should always take in account the stability of the compound resulting from a de-protonated or protonated (or accepting or donating electrons). If the resulting molecule is more stable (e.g. some resonance effect occur) the reaction is favorite. This is the case of acidity of the phenol! | |
| Jan 5, 2014 at 10:28 | review | First posts | |||
| Jan 5, 2014 at 13:44 | |||||
| Jan 5, 2014 at 10:09 | history | asked | atmosx | CC BY-SA 3.0 |