Chapter 4: Q4-4-5 (page 89)
Draw the structures of the following molecules:
(a) trans-1-Bromo-3-methylcyclohexane
(b) cis-1,2-Dimethylcyclobutane
(c) trans-1-tert-Butyl-2-ethylcyclohexane
Short Answer
a)
b)
c)
Chapter 4: Q4-4-5 (page 89)
Draw the structures of the following molecules:
(a) trans-1-Bromo-3-methylcyclohexane
(b) cis-1,2-Dimethylcyclobutane
(c) trans-1-tert-Butyl-2-ethylcyclohexane
a)
b)
c)
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Get started for freeDraw a stereoisomer of trans-1, 3-dimethylcyclobutane.
One of the two chair structures of cis-1-chloro-3-methylcyclohexane is more stable than the other by 15.5 kJ/mol (3.7 kcal/mol). Which is it? What is the energy cost of a 1,3-diaxial interaction between chlorine and a methyl group?
Two conformations of cis-1,3-dimethylcyclobutane are shown. What is the difference between them, and which do you think is likely to be more stable?
Assume that you have a variety of cyclohexane substituted in the positions indicated. Identify the substituents as either axial or equatorial. For example, a 1, 2-cis relationship means that one substituent must be axial and one equatorial, whereas a 1, 2-trans relationship means that either substituent is axial or both are equatorial.
(a) 1, 3-Trans disubstituted (b) 1, 4-Cis disubstituted
(c) 1, 3-Cis disubstituted (d) 1, 5-Trans disubstituted
(e) 1, 5-Cis disubstituted (f) 1, 6-Trans disubstituted
Name the following compound, identify each substituent as axial or equatorial, and tell whether the conformation shown is the more stable or less stable chair form
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