Chair Conformation and Ring Flips
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- Опубліковано 4 сер 2024
- This organic chemistry video tutorial provides a basic introduction into drawing the chair conformation of cyclohexane and identifying the most stable conformation of Methylcyclohexane and 1-tert-butyl-4-methylcyclohexane. It also discusses how to perform a ring flip by adjusting the appropriate axial bonds and equatorial bonds. It also explains what type of reaction arrow to use This video contains plenty of examples and practice problems.
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I think the equatorial position should be parallel to the C -C bond either to the right or left. I have noticed that you have made some mistakes in drawing the correct structure. Otherwise, you the best tutor that I would always like your videos that simplifies everything. thank you very much.
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At 16:20, when you're doing a chair flip from form B to form A, you said that you move the carbons in a couterclockwise direction, but is it necessary to reverse the direction of the carbons, or just move them back one place? By the way, your videos are amazing, and I use them for practically every subject in school! Thank you so much!
Im confused on how you know if the substituents is either axial or equatorial and if they are up or down on on the chair. I understand the ring flip and which one would be more stable but I just dont understand the inital drawing process, someone plzzzzzzzzzz help
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For the first cyclohexane on number 5, wouldn't you start numbering at the bromine atom since halogens are the priority group in this case?
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