Draw the substituents in the specified locations on the given cyclohexane ring to show the most stable chair conformation. Be sure that the bonds are drawn toclearly show whether they are axial or equatorial.SubstituentPositionOH1CH,2CI5छCI6C C9c

Answered: Draw the substituents in the specified…

Chemistry

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ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Draw the substituents in the specified locations on the given cyclohexane ring to show the most stable chair conformation. Be sure that the bonds are drawn to clearly show whether they are axial or equatorial. CH₂ 1 Substituent Position Br 5 3 5 3 Q C C с X ㅃ E Jh Cx C 00 olo Ar 18 K
Draw the substituents in the specified locations on the given cyclohexane ring to show the most stable chair conformation. Be sure that the bonds are drawn to clearly show whether they are axial or equatorial. Substituent Position OH 1 OH 3 F 4 CH, 5
Draw the substituents in the specified locations on the given cyclohexane ring to show the most stable chair conformation. Be sure that the bonds are drawn to clearly show whether they are axial or equatorial. 6 Substituent Position CH 3 1 Br 3 5 3
Complete the given chair conformation of cyclohexane by adding the listed substituents to the specified position and bond direction. Substituent Position Bond direction CH3 CH3 OH F 3 6 1 3 axial axial equatorial equatorial
9
Draw the structure for the most stable chair conformation of trans-1-tert-butyl-3-chlorocyclohexane. Use the cyclohexane conformation drawing tool and guide points to draw each structure. C1 M C™ X Ĉ
Draw a Newman projection for two more staggered conformations of this molecule. Which of your conformations is most stable? Assume that -OH and -CH3 are comparable in size.
Following is a planar hexagon representation for one isomer of 1,2,4-trimethylcyclohexane. Draw the alternative chair conformations of this compound and state which of the two is more stable. H,C CH3 H H H CH3
Consider the isomers of tert-butylcyclohexanol in conformational structures. Two are cis-2-tert-butylcyclohexanol and two are cis-3-tert-butylcyclohexanol. Indicate which is the more stable conformation for each pair, and indicate which of all four conformations is the most stable. FIX a box OH HO OH A Select the more stable conformation of cis-2-tert-butylcyclohexanol. B OD C B C D ☐A C OH Select the more stable conformation of cis-3-tert-butylcyclohexanol.
11. Which one of these forms of 1,2,4-trimethylcyclohexane can have a chair conformation in which the methyl groups are all equatorial? III ++ |||| A B с D E
None
Starting from the wedge-and-dash structure below, rotate the back carbon to provide the Newman projection in the most stable conformation. H3C H Br H H3C H Q

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Draw the substituents in the specified locations on the given cyclohexane ring to show the most stable chair conformation. Be sure that the bonds are drawn to clearly show whether they are axial or equatorial. Substituent Position OH 1 CH, 2 CI 5 छ CI 6 C C 9 c