Chair Conformation and Ring Flips
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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Жыл бұрын
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Жыл бұрын
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2 жыл бұрын
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2 жыл бұрын
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2 жыл бұрын
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2 жыл бұрын
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@vallariashar3179
3 жыл бұрын
unive- isn't this high school level stuff?
@kurooackerman7338
3 жыл бұрын
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@vallariashar3179
3 жыл бұрын
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3 жыл бұрын
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@Veronicz
3 жыл бұрын
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6 ай бұрын
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6 ай бұрын
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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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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
@imanifreefun
3 жыл бұрын
Hi @Mohamed Dahcheh, this video helped me understand the placement of substituents! kzread.info/dash/bejne/ZqyCs9momLa4ktI.html Good luck!
@bet3324
2 жыл бұрын
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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!
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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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