Timeline for How does chloroform react with cyclopentadiene in base?
Current License: CC BY-SA 4.0
5 events
| when toggle format | what | by | license | comment | |
|---|---|---|---|---|---|
| Jul 13, 2021 at 10:31 | comment | added | Rishi | @NuclearChemist In your first paragraph, last line you state that, "* This anion is an aromatic species which is unlikely to be able to react with the carbene.*" Why?, In reimer teimann reaction it is completely fine for the aromaticity to break momentarily? | |
| Apr 28, 2019 at 16:07 | history | edited | orthocresol | CC BY-SA 4.0 |
deleted 75 characters in body
|
| Jun 6, 2018 at 0:42 | vote | accept | Avyansh Katiyar | ||
| Jun 3, 2018 at 9:12 | comment | added | Waylander | The abstract of this paper pubs.rsc.org/en/content/articlelanding/1971/c2/… records that under very similar conditions the product of cyclopentadiene and dichlorocarbene is 6-Cl-fulvene. It is behind a paywall so I cannot read the full paper. | |
| Jun 3, 2018 at 6:35 | history | answered | Nuclear Chemist | CC BY-SA 4.0 |