Timeline for Why does fructose reduce Tollen's reagent and Fehling's solution?
Current License: CC BY-SA 3.0
9 events
| when toggle format | what | by | license | comment | |
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| May 8, 2021 at 0:46 | review | Suggested edits | |||
| May 8, 2021 at 4:15 | |||||
| Mar 15, 2018 at 15:19 | comment | added | Gaurang Tandon | This answer nicely elaborates the mechanism stated in words in this answer. | |
| May 26, 2017 at 10:20 | comment | added | MrObjectOriented | However, everywhere, it is written only 'alpha-hydroxy ketones'. Not all alpha-hydroxy ketones are fructose, that is, not all alpha hydroxy ketones can double tautomerization to form an aldehyde. | |
| Nov 14, 2016 at 14:17 | history | edited | user7951 | CC BY-SA 3.0 |
added 2 characters in body
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| S Feb 24, 2016 at 19:42 | history | suggested | Nilay Ghosh | CC BY-SA 3.0 |
improved formatting
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| Feb 24, 2016 at 19:32 | review | Suggested edits | |||
| S Feb 24, 2016 at 19:42 | |||||
| Nov 6, 2015 at 15:58 | vote | accept | Nilay Ghosh | ||
| Nov 6, 2015 at 15:54 | vote | accept | Nilay Ghosh | ||
| Nov 6, 2015 at 15:58 | |||||
| Nov 6, 2015 at 14:28 | history | answered | user7951 | CC BY-SA 3.0 |