Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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  1. Build a model of 2,2,5,5-tetramethylhexane.
  2. Orient the model so that you are looking at the carbon with the arrow pointing to it in Figure 3. Align the bond to the next carbon in the chain so that it is directly behind the first carbon to match a Newman projection view. (See Figure MM.3 in the lab manual)
  3. Spin the carbons on either side of the bond you're looking down to cycle through all three staggered and all three eclipsed positions of the substituents.
  4. Draw all six positions as Newman projections on the data sheet and identify the position with the highest energy. Draw the six Newman projections of all of the different energy levels. Label each as staggered or eclipsed and rank in order from lowest energy to highest.

 

H3C
H3C-
st Edi
CH3
CH3
CH3
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Transcribed Image Text:H3C H3C- st Edi CH3 CH3 CH3
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Are these in order of highest energy to lowest energy? What would be that order? 

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Are these in order of highest energy to lowest energy? What would be that order? 

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