Timeline for Stability order of carbocations
Current License: CC BY-SA 4.0
7 events
| when toggle format | what | by | license | comment | |
|---|---|---|---|---|---|
| Feb 11, 2019 at 19:11 | comment | added | Martin - マーチン♦ | I inserted a link to the paper I could find, I don't have the time to look for the other 'reference'. I found two candidates be Olah et.al.; DOI: 10.1021/ja00761a041; 10.1021/ja00761a042 | |
| Feb 11, 2019 at 19:05 | history | edited | Martin - マーチン♦ | CC BY-SA 4.0 |
removed thanks, inserted links
|
| Feb 11, 2019 at 18:58 | comment | added | Martin - マーチン♦ | Given the evidence in the linked post, I'd say this is not correct in its entirety. | |
| Feb 11, 2019 at 11:45 | comment | added | Alchimista | en.m.wikipedia.org/wiki/Tropylium_cation | |
| Feb 11, 2019 at 11:36 | comment | added | Arpit Kumar | I know D is a very stable carbocation due to aromaticity. However, the cyclopropylmethyl carbocation is exceptionally stable deu to its bend orbital bond i.e. a non conventional resonance(popularily called dancing resonance). However you dont seem to have accounted for it in your answer......... | |
| Feb 11, 2019 at 11:15 | review | First posts | |||
| Feb 11, 2019 at 11:33 | |||||
| Feb 11, 2019 at 11:13 | history | answered | John | CC BY-SA 4.0 |