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Organic Chemistry: Cyclohexane ring flip

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Uploaded by on May 20, 2010

Cyclohexane ring flip of cis-1-1ethyl-4-fluorocylcohexane

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  • so two quick questions, had you placed the fluorine on the equatorial down position (as opposed to the up axial) then would that be Trans -1-ethyl-4-flourocyclohexane ? also would it be right to place the ethyl on an axial down position and then the flouro would be on an equatorial down as well ? thanks

  • thank you !!!!!!! :)

  • thanks man for clearing up my confusion

  • nice job explaining!

  • Thanks for sharing, this helped clarity some confusion!

  • I guess the first ring is more stable because the larger substituent (ethyl) is in the equatorial position.

  • THANK YOUTHANK YOUTHANK YOUTHANK YOUTHANK YOUTHANK YOUTHANK YOUTHANK YOUTHANK YOUTHANK YOUTHANK YOU

  • Ah nice, this was way easier to follow than my textbook. Thank you!

  • thank you. :)

    

  • thank you so much!! you have made ring flip and stability understandable!!! great explanation!

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