Chapter 3: Q17P (page 168)
Question: Which of the following cycloalkanes are capable of geometric (cis-trans) isomerism? Draw the cis and trans isomers
(a)
(b)
(c)
(d)
Short Answer
A)
B)
C)
D)
Chapter 3: Q17P (page 168)
Question: Which of the following cycloalkanes are capable of geometric (cis-trans) isomerism? Draw the cis and trans isomers
(a)
(b)
(c)
(d)
A)
B)
C)
D)
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Get started for freeUse your models to do a chair-chair interconversion on each ring of the conformation of shown in Figure 3-27. Draw the conformation that results.
The following names are all incorrect or incomplete, but they represent real structures. Draw each structure and name it correctly.
(a)
(b)
(c)
(d)
(e)
(f)
Using what you know about the conformational energetics of substituted cyclohexanes, predict which of the two isomers is more stable. Explain your reasoning.
Table 3-6 shows that the axial-equatorial energy difference for methyl, ethyl, and isopropyl groups increases gradually: 7.6, 7.9 and 8.8 kJ/mol (1.8, 1.9, and 2.1 kcal/mol). The tert-butyl group jumps to an energy difference of 23 kJ/mol (5.4 kcal/mol), over twice the value for the isopropyl group. Draw pictures of the axial conformations of isopropylcyclohexane and tert-butylcyclohexane and explain why the tert-butyl substituent experiences such a large increase in axial energy over the isopropyl group.
Give the IUPAC name of the following alkanes.
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
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