Timeline for How to determine the most reactive hydroxyl group of α-ᴅ-glucopyranose?
Current License: CC BY-SA 3.0
5 events
| when toggle format | what | by | license | comment | |
|---|---|---|---|---|---|
| Jan 12, 2020 at 18:39 | vote | accept | justbehappy | ||
| Aug 12, 2015 at 11:32 | vote | accept | justbehappy | ||
| Jan 12, 2020 at 17:09 | |||||
| Jun 18, 2015 at 17:28 | comment | added | Jori | @Jan Sure it's a hemi-acetal, thanks for pointing that out. I figured that OP's knowledge of chemistry is not very developed yet so I circumvented using the term. Again, thanks for your input. | |
| Jun 18, 2015 at 17:02 | comment | added | Jan | Might be worth mentioning that the big difference of the $\alpha$ carbon is its oxidation state: Formally it's an aldehyde, not an alcohol. And in the OP's figure, one would call it hemi-acetal. | |
| Jun 18, 2015 at 14:47 | history | answered | Jori | CC BY-SA 3.0 |