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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Chapter1: Chemical Foundations
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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
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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