6. In the following exercise, you will use the name of the compound given to draw the substituted cyclohexane rings in both chair conformations (i.e. before and after a "ring/chair flip"). Draw the axial and equatorial positions ONLY ON the carbons indicated in the name of the compound, please leave all other carbons alone. Circle the lowest energy conformation of each structure. A table of 1,3-diaxial steric strain values required for this analysis is found on the next page. a. cis-2-bromo-1-methylcyclohexane b. cis-3-isopropyl-1-methylcyclohexane c. cis-4-chloro-1-hydroxycyclohexane. (a hydroxy group is an OH group) d. trans-4-chloro-1-ethylcyclohexane e. trans-3-tert-butyl-1-ethylcyclohexane
6. In the following exercise, you will use the name of the compound given to draw the substituted cyclohexane rings in both chair conformations (i.e. before and after a "ring/chair flip"). Draw the axial and equatorial positions ONLY ON the carbons indicated in the name of the compound, please leave all other carbons alone. Circle the lowest energy conformation of each structure. A table of 1,3-diaxial steric strain values required for this analysis is found on the next page. a. cis-2-bromo-1-methylcyclohexane b. cis-3-isopropyl-1-methylcyclohexane c. cis-4-chloro-1-hydroxycyclohexane. (a hydroxy group is an OH group) d. trans-4-chloro-1-ethylcyclohexane e. trans-3-tert-butyl-1-ethylcyclohexane
Chemistry
10th Edition
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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