Timeline for Why is a rearrangement observed for the secondary alcohol but not the primary in these examples?
Current License: CC BY-SA 3.0
7 events
| when toggle format | what | by | license | comment | |
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| May 9, 2016 at 15:53 | history | tweeted | twitter.com/StackChemistry/status/729700831323394049 | ||
| May 6, 2016 at 14:49 | vote | accept | J. Doe | ||
| May 6, 2016 at 11:54 | history | edited | Jan | CC BY-SA 3.0 |
Spelt out the bromide and hydrogen, better title.
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| May 6, 2016 at 11:51 | answer | added | Jan | timeline score: 5 | |
| May 6, 2016 at 11:08 | comment | added | Karl | Predicting the pathway for these Wagner-Meerwein rearrangements is rather hard, isn't it? Usually you get a lot of side products. | |
| May 6, 2016 at 8:36 | comment | added | ringo | Consider the preferred pathway for a 2º alcohol vs a 1º alcohol. | |
| May 6, 2016 at 8:26 | history | asked | J. Doe | CC BY-SA 3.0 |