5. (3 pts) a- Convert the following Newman projection into the bond line structural formula. Must use stereobonds to indicate the orientation of the groups. CN H H3CO H b- Draw the anti, gauche, and eclipsed conformations of the following molecule using Newman projection. H Η H H c- i. Which cyclopropane molecule has the highest torsional strain? ii. Which cyclopropane molecule has the lowest torsional strain? с b a
5. (3 pts) a- Convert the following Newman projection into the bond line structural formula. Must use stereobonds to indicate the orientation of the groups. CN H H3CO H b- Draw the anti, gauche, and eclipsed conformations of the following molecule using Newman projection. H Η H H c- i. Which cyclopropane molecule has the highest torsional strain? ii. Which cyclopropane molecule has the lowest torsional strain? с b a
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:5. (3 pts)
a- Convert the following Newman projection into the bond line structural formula.
Must use stereobonds to indicate the orientation of the groups.
CN
H
H3CO
H
b- Draw the anti, gauche, and eclipsed conformations of the following molecule
using Newman projection.
H
Η
H
H
c- i. Which cyclopropane molecule has the highest torsional strain?
ii. Which cyclopropane molecule has the lowest torsional strain?
с
b
a
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