File:Mechanism for the Reaction of N-tert-butylbenzenesulfinimidoyl chloride With an Alkoxide.png
Size of this preview: 800 × 188 pixels. Other resolutions: 320 × 75 pixels | 640 × 150 pixels | 3,012 × 708 pixels.
Original file (3,012 × 708 pixels, file size: 70 KB, MIME type: image/png)
 | This is a file from the Wikimedia Commons. Information from its description page there is shown below. Commons is a freely licensed media file repository. You can help. |
Summary
| Description |
English: N-tert-butylbenzenesulfinimidoyl is an oxidizing agent that reacts with secondary and primary alkoxides to give ketones and aldehydes, respectively. The elimination reaction responsible for the new double bond occurs via a five-membered ring transition state. |
| Date | |
| Source | Own work |
| Author | Ckalnmals |
Licensing
I, the copyright holder of this work, hereby publish it under the following license:
This file is licensed under the Creative Commons Attribution-Share Alike 3.0 Unported license.
- You are free:
- to share – to copy, distribute and transmit the work
- to remix – to adapt the work
- Under the following conditions:
- attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
- share alike – If you remix, transform, or build upon the material, you must distribute your contributions under the same or compatible license as the original.
File history
Click on a date/time to view the file as it appeared at that time.
| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 03:11, 26 June 2012 | | 3,012 × 708 (70 KB) | Ckalnmals |
File usage
The following page uses this file:
