Timeline for Friedel-Crafts Alkylation and hybridization
Current License: CC BY-SA 3.0
7 events
| when toggle format | what | by | license | comment | |
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| Apr 8, 2017 at 1:25 | history | edited | pentavalentcarbon |
had the obsolete reaction tag, added carbocation and halide tags
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| Feb 15, 2015 at 18:05 | vote | accept | Dissenter | ||
| Jan 31, 2015 at 18:11 | history | edited | ron | CC BY-SA 3.0 |
spelling
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| Jan 31, 2015 at 17:34 | comment | added | ron | You can do this. As @jerepierre has noted the intermediates involved are higher in energy and consequently more reactive once generated. But under controlled conditions the reaction does work. You just need to use a stronger lewis acid than an aluminum trihalide. Google "Friedel Crafts alkenylation". | |
| Jan 31, 2015 at 16:32 | history | tweeted | twitter.com/#!/StackChemistry/status/561562555060334592 | ||
| Jan 31, 2015 at 13:06 | answer | added | jerepierre | timeline score: 2 | |
| Jan 31, 2015 at 7:31 | history | asked | Dissenter | CC BY-SA 3.0 |