Chapter 3: 41P (page 189)
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)
Short Answer
(a)
(b)
(c)
(d)
(e)
(f)
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Chapter 3: 41P (page 189)
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)
(a)
(b)
(c)
(d)
(e)
(f)
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Use a Newman projection about the indicated bond to draw the most stable conformer for each compound.
(a)
(b)
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.
Draw the two chair conformations of each compound, and label the substituents as axial and equatorial. In each case, determine which conformation is more stable.
(a)
(b)
(c)
(d)
(e)
(f)
In each pair of compounds, which compound has the higher boiling point? Explain your reasoning.
(a) Nonane or 3-methylheptane
(b) Octane or 2,3,4-trimethylpentane
(c) 2,3,5-trimethylhexane or nonane
Name the following alkane and haloalkane. When two or more are present list them in alphabetical order.

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