Consider the cyclohexane framework in a chair conformation, where carbon 1 has two substituents, X and Y. a. Label each position as axial or equatorial. b. On the same figure, label all positions that are gauche to the Y group on carbon 1. A bin may hold more than one label. axial equatorial X 1 equatorial equatorial 2 axial axial axial gauche 3 axial gauche 5 equatorial equatorial 4 axial equatorial Answer Bank equatorial gauche axial

Consider the cyclohexane framework in a chair conformation, where carbon 1 has two substituents, X and Y. a. Label each position as axial or equatorial. b. On the same figure, label all positions that are gauche to the Y group on carbon 1. A bin may hold more than one label. axial equatorial X 1 equatorial equatorial 2 axial axial axial gauche 3 axial gauche 5 equatorial equatorial 4 axial equatorial Answer Bank equatorial gauche axial

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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Which of the following Newman projections is NOT a conformational isomer of 1,2-dibromoethane? Br H BrH Br H Br Br B.H- D. H- A. С. H- -Br -H- Br H. H Br HH H H H H
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a. Draw the structure of this molecule as a hexagon with dash(es) and/or wedge(s). ha -OH b. Draw the other chair conformation. c. Draw the enantiomer of the molecule in its most stable conformation. он H d. Ignoring differences in conformation, how is this molecule related to the one above? Are they the Same molecule, Enantiomers, or Diastereomers? OH H₂ HH₂ POM (CH₂)2
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Which of the following projections would the most stable? I believe that it would be the 6th because out of all 6 groups, the methyl groups are the furthest distance away from each other in the 6th. When they are in close proximity, the front and back methyl groups’ electron orbitals repel each other, which generates potential energy and makes the conformation unstable.
5. Draw a Newman projection of 1,2-dichloroethane in the eclipsed, gauche and staggered position. 6. Build a model of 3,3-dimethylhexane. Draw a Newman projection of the most stable conformer of 3,3-dimethylhexane sighting down the C2-C3 bond.
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Chair Conformer = axial bond > = equatorial bond Draw 1,2,3,4,5,6-hexachlorocyclohexane with a. all the chloro groups in axial positions. b. all the chloro groups in equatorial positions.