Chapter 3: Q18P (page 168)
Give IUPAC names for the following cycloalkanes.
(a)
(b)
(c)
Short Answer
(a)cis-1-ethyl-3-methylcyclobutane
(b)trans-1-tert-butyl-3-ethyl cyclohexane
(c)trans-1,2-dimethyl cyclopropane
Chapter 3: Q18P (page 168)
Give IUPAC names for the following cycloalkanes.
(a)
(b)
(c)
(a)cis-1-ethyl-3-methylcyclobutane
(b)trans-1-tert-butyl-3-ethyl cyclohexane
(c)trans-1,2-dimethyl cyclopropane
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Get started for freeDraw Newman projection, similar to Figure 3-25, down the C1-C6 bond in the equatorial conformation of methylcyclohexane. Show that the equatorial methyl group is also anti toC5. (Using your models will help.)
Construct a graph, similar to Figure 3-11, of the torsional energy of along the.Placein front, represented by three bonds coming together in a Y shape, andin back, represented by a circle with three bonds pointing out from it. Define the dihedral angle as the angle between the methyl group on the front carbon and ethyl group on the back carbon. Begin your graph at thedihedral angle and begin to turn the front carbon. Show the Newman projection and the approximate energy at eachof rotation. Indicate which conformations are the most stable (lowest energy) and the least stable (highest energy).
Question: The most stable form of 1,2,3,4,5,6-Cyclohexanehexolcontains a six-membered ring in the chair conformation with all the substituents equatorial. Draw this most stable conformation of cyclohexanehexol
Question: This is a Newman projection of a substituted cyclohexane.
(a) Draw the equivalent chair form
(b)Draw the equivalent structure using wedge and dash notation on a cyclohexane hexagon.
(c) Give the IUPAC name.
Use a Newman projection about the indicated bond to draw the most stable conformer for each compound.
(a)
(b)
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