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| Description |
English: Skeletal structures for the organic oxidation) of a pyrrolidine hydroxylamine using mercuric oxide to give a nitrone. |
| Date | |
| Source | Own work |
| Author | DMacks (talk) |
|
This image of a simple structural formula is ineligible for copyright and therefore in the public domain, because it consists entirely of information that is common property and contains no original authorship. |  |
File history
Click on a date/time to view the file as it appeared at that time.
| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 23:47, 4 December 2015 | | 1,271 × 460 (34 KB) | DMacks | Let's try that again. grr |
| 22:21, 4 December 2015 |  | 1,271 × 460 (34 KB) | DMacks | fix N=C bond display | |
| 22:12, 4 December 2015 |  | 1,271 × 460 (34 KB) | DMacks | Redraw from scratch for various MOS reasons: alignment of N–O bond in reactant, non-use of ambiguous "Me" for methyl group, more scalable. | |
| 00:39, 27 June 2010 |  | 269 × 99 (8 KB) | OrganicReactions | yield | |
| 21:27, 5 June 2010 |  | 280 × 83 (9 KB) | OrganicReactions | {{Information |Description={{en|1=nitrone-olefin cycloaddition}} |Source={{own}} |Author=OrganicReactions |Date= |Permission= |other_versions= }} Category:Organic chemistry |
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