13. Given the following interactions, what is the difference in the amount of strain associated with the conformations show Me/Me gauche: 0.9 kcal/mol Me/H 1,3-diaxial: 0.9 kcal/mol OH/H 1,3-diaxial: 0.25 kcal/mol (A) 0.4 kcal/mol (B) 0.9 kcal/mol OH Me -Me Me ring inversion HO Me (C) 1.3 kcal/mol (D) 1.8 kcal/mol Me Me if th EU an
13. Given the following interactions, what is the difference in the amount of strain associated with the conformations show Me/Me gauche: 0.9 kcal/mol Me/H 1,3-diaxial: 0.9 kcal/mol OH/H 1,3-diaxial: 0.25 kcal/mol (A) 0.4 kcal/mol (B) 0.9 kcal/mol OH Me -Me Me ring inversion HO Me (C) 1.3 kcal/mol (D) 1.8 kcal/mol Me Me if th EU an
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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Transcribed Image Text:13. Given the following interactions, what is the difference in the amount of strain associated with the conformations show
Me/Me gauche: 0.9 kcal/mol
Me/H 1,3-diaxial: 0.9 kcal/mol
OH/H 1,3-diaxial: 0.25 kcal/mol
F
CI
OH
-F
(B)
CI
Me
-Me
Me
(A) 0.4 kcal/mol (B) 0.9 kcal/mol (C) 1.3 kcal/mol
(D) 1.8 kcal/mol
14. Which structure represents the most stable conformation of trans-1-chloro-3-fluorocyclohexane if the F/H and
interactions are 0.12 and 0.25 kcal/mol, respectively?
CI
ring inversion
A
F
(A)
(C)
15. Which compound is chiral and can exist as a pair of enantiomers?
(A) cis-1,3-dimethylcyclobutane
(B) trans-1,3-dimethylcyclobutane
(C) cis-1,2-dimethylcyclobutane
(D) trans-1,2-dimethylcyclobutane
HO Me
Me
(D)
Me
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