Timeline for Stability of tertiary carbocation [duplicate]
Current License: CC BY-SA 4.0
8 events
| when toggle format | what | by | license | comment | |
|---|---|---|---|---|---|
| Dec 22, 2018 at 16:10 | history | closed |
Mithoron andselisk♦ user7951 |
Duplicate of What is the reason for the exceptional stability of the cyclopropylmethyl carbocation? | |
| Dec 22, 2018 at 16:05 | review | Close votes | |||
| Dec 22, 2018 at 16:10 | |||||
| Dec 22, 2018 at 5:59 | comment | added | Jan | chemistry.stackexchange.com/q/19090 Half-way dupe. If I vote to close it will be close-hammered because of my badge so I will leave it to others to decide if this is dupe-y enough. | |
| Dec 22, 2018 at 5:57 | comment | added | Yusuf Hasan | Related: chemistry.stackexchange.com/q/48264/54655 | |
| Dec 22, 2018 at 5:54 | answer | added | Lakshya Sinha | timeline score: -3 | |
| Dec 22, 2018 at 5:35 | history | edited | Jan | CC BY-SA 4.0 |
Better wording
|
| Dec 22, 2018 at 5:34 | comment | added | Jan | It is not called ‘three degree’, it is tertiary. Likewise, they are secondary and primary carbocations. The degree notation should have died out a long time ago. | |
| Dec 22, 2018 at 4:49 | history | asked | sauhaard batra | CC BY-SA 4.0 |