3.Look along any bond connecting any two carbon atoms in the ring. (Rotate the r
ID: 811616 • Letter: 3
Question
3.Look along any bond connecting any two carbon atoms in the ring. (Rotate the ring and look along a new pair of carbon atoms.) How are the bonds connected to these two carbons arranged? Are they staggered or are they eclipsed (3a)? In the space provided on the Report Sheet (3b), draw the Newman projection for the view (see Experiment 21 for an explanation of this projection); for the bond connecting a ring carbon, label that group ring. 4. Pick up the cyclohexane model and view it from the side of the chair. Visualize the ring around the perimeter of the system perpendicular to the axis through the center. Of the 12 hydrogens, how many are pointed up relative to the plane (4a)? How many are pointed down (4b)? 5. Orient your model so that you look at an edge of the ring and it conforms to Figure 22.3. Are the two axial positions labeled A cis or trans to each other (5a)? Are the two equatorial positions labeled B cis or trans to each other (5b)? Are the axial and equatorial positions A and B cis or trans to each other (5c)? Rotate the ring and view new pairs of carbons in the same way. See whether the relationships of positions vary from the above. Position your eye as in Figure 22.3 and view along the carbon - carbon bond. In the space provided on the Report Sheet (5d), draw the Newman projection. Using this projection, review your answers to 5a, 5b, and 5c.Explanation / Answer
3.Look along any bond connecting any two carbon atoms in the ring. (Rotate the r
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