Chapter 4: Q.46. (page 128)
Question: Considering rotation around the bond highlighted in pink in each compound, draw Newman projections for the most stable and least stable conformations.
a.
b.
Short Answer
Answer
a.
b.
Chapter 4: Q.46. (page 128)
Question: Considering rotation around the bond highlighted in pink in each compound, draw Newman projections for the most stable and least stable conformations.
a.
b.
Answer
a.
b.
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Get started for freeQuestion: a.Draw the three staggered and three eclipsed conformations that result from rotation around the bond labeled in red using Newman projections. b. Label the most stable and least stable conformation.
Question: Consider the substituted cyclohexane shown in the ball-and-stick model.
Question: Draw the three constitutional isomers having molecular formula that contain a five-membered ring and two methyl groups as substituents. For each constitutional isomer that can have cis and trans isomers, draw the two stereoisomers.
Question: The eclipsed conformation of is role="math" localid="1648620042367" less stable than the staggered conformation. How much is the H, Cl eclipsing interaction worth in destabilization?
Question: Draw the structure corresponding to each IUPAC name.
a. 3-ethyl-2-methylhexane
b. sec-butylcyclopentane
c. 4-isopropyl-2,4,5-trimethylundecane
d. cyclobutylcycloheptane
e. 3-ethyl-1,1-dimethylcyclohexane
f. 4-butyl-1,1-diethylcyclooctane
g. 6-isopropyl-2,3-dimethyldodecane
h. 2,2,6,6,7-pentamethyloctane
i. cis-1-ethyl-3-methylcyclopentane
j. trans-1-tert-butyl-4-ethylcyclohexane
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