Chapter 3: 46P (page 190)
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)
Chapter 3: 46P (page 190)
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)
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Get started for freeQuestion: Using the general formula for alkanes
(a) Predict the molecular formula of thestraight chain alkane.
(b) Predict the molecular formula of the alkanes containing 42 carbon atom with extensive branching.
Draw the structure and give the molecular formula for each of the following compounds.
(a) 1-ethyl-3-methylcycloheptane
(b) isobutylcyclohexane
(c) cyclopropylcyclopentane
(d) 3-ethyl-1,1-dimethylcyclohexane
(e) 3-ethyl-2,4-dimethylhexane
(f) 1,1-diethyl-4-(3,3-dimethylbutyl)cyclohexane
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.
(a) Draw and name the five cycloalkane structures of formula. Can any of these structures give rise to geometric (cis-trans) isomerism? If so, show the cis and trans stereoisomers.
(b) Draw and name the eight cycloalkane structures of formulathat do not show geometric isomerism.
(c) Draw and name the four cycloalkanes of formulathat do have cis-trans isomerism.
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