Timeline for How to explain (non-/anti-) aromaticity in fulvene with the help of resonance structures?
Current License: CC BY-SA 4.0
15 events
when toggle format | what | by | license | comment | |
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Apr 21 at 9:07 | history | edited | Loong | CC BY-SA 4.0 |
added 4 characters in body
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Sep 14, 2017 at 13:32 | history | edited | Martin - マーチン♦ | CC BY-SA 3.0 |
reformulated title as question
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Sep 14, 2017 at 13:28 | answer | added | Martin - マーチン♦ | timeline score: 6 | |
Sep 14, 2017 at 8:13 | history | reopened |
Oscar Lanzi Martin - マーチン♦ |
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Sep 14, 2017 at 1:28 | review | Reopen votes | |||
Sep 14, 2017 at 8:13 | |||||
Sep 14, 2017 at 1:11 | comment | added | Oscar Lanzi | Structure 1 has pendant pi bonding. The Huckel rules require a cycle of conjugated electrons and that does not go with pendant pi bonds. | |
Sep 10, 2017 at 9:46 | comment | added | Sawarnik | Well just apply the Huckel rules and see there's 4 electrons in conjugation in (2) while (1) is not fully conjugated. | |
Sep 5, 2017 at 8:28 | review | Reopen votes | |||
Sep 5, 2017 at 13:47 | |||||
Sep 5, 2017 at 8:12 | history | edited | andselisk♦ | CC BY-SA 3.0 |
Added ACS-complient CG-structures, put title into question as OP attempt to solve the problem, generalized title
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Sep 5, 2017 at 7:56 | history | edited | Amruta Koshe | CC BY-SA 3.0 |
edited title
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Sep 4, 2017 at 18:31 | history | closed |
Oscar Lanzi Tyberius♦ Mithoron Linear Christmas M.A.R. |
Not suitable for this site | |
Sep 4, 2017 at 17:16 | history | edited | user7951 | CC BY-SA 3.0 |
edited title
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Sep 4, 2017 at 16:43 | review | Close votes | |||
Sep 4, 2017 at 18:31 | |||||
Sep 4, 2017 at 16:10 | review | First posts | |||
Sep 4, 2017 at 18:30 | |||||
Sep 4, 2017 at 16:06 | history | asked | Amruta Koshe | CC BY-SA 3.0 |