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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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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.
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When ring flip happens completely from chair-to-chair, hydrogens that were previously axial (blue H) turn equatorial & equatorial ones (red H) turn axial.
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Pink and orange arrows show how one can imagine how carbons are being "pushed" as one conformation turns into another.
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I, the copyright holder of this work, hereby publish it under the following license:
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The person who associated a work with this deed has dedicated the work to the
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J Clayden, N Greeves, SG Warren (2001). Organic chemistry. (2nd ed.). p. 373.
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Source for the conformation names & claim of lowest/highest energy:
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Click on a date/time to view the file as it appeared at that time.
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copyrighted, dedicated to the public domain by copyright holder
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http://creativecommons.org/publicdomain/zero/1.0/deed.en
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