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Summary
| Description |
English: Cyclohexane chair flip (ring inversion) reaction. Structures of the significant conformations (A, B, C & D) of the reaction are shown. Inversion happens quickly & constantly in room temperature.
Conformations: 1: chair (lowest in energy) 2: half-chair (highest in energy) 3: twist-boat 4: boat When ring flip happens completely from chair-to-chair, hydrogens that were previously axial (blue H) turn equatorial & equatorial ones (red H) turn axial. Pink and orange arrows show how one can imagine how carbons are being "pushed" as one conformation turns into another. Source for the conformation names & claim of lowest/highest energy:
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| Date | |
| Source | Own work |
| Author | Keministi |
| SVG development |  This chemical equation was created with an unknown SVG tool.  |
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I, the copyright holder of this work, hereby publish it under the following license:
 
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This file is made available under the Creative Commons CC0 1.0 Universal Public Domain Dedication. |
| The person who associated a work with this deed has dedicated the work to the public domain by waiving all of their rights to the work worldwide under copyright law, including all related and neighboring rights, to the extent allowed by law. You can copy, modify, distribute and perform the work, even for commercial purposes, all without asking permission.
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 18:48, 19 September 2018 | | 462 × 157 (23 KB) | 5-HT2AR | User created page with UploadWizard |
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