Chapter 4: Q4-31E (page 114)
Draw three isomers of trans-1, 2-dichlorocyclobutane, and label them as either constitutional isomers or stereoisomers.
Short Answer
The three isomers oftrans-1, 2-dichlorocyclobutane are as follow;

Chapter 4: Q4-31E (page 114)
Draw three isomers of trans-1, 2-dichlorocyclobutane, and label them as either constitutional isomers or stereoisomers.
The three isomers oftrans-1, 2-dichlorocyclobutane are as follow;

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cis-1, 2-Dimethylcyclobutane is less stable than its trans isomer, but cis-1, 3-dimethylcyclobutane is more stable than its trans isomer. Draw the most stable conformations of both, and explain.
Draw two constitutional isomers of.
cis-1,2-Dimethylcyclopropane has more strain than trans-1,2-dimethylcyclopropane. How can you account for this difference? Which of the two compounds is more stable?
In light of your answer to Problem 4-48, draw the two chair conformations of 1,1,3-trimethylcyclohexane and estimate the amount of strain energy in each. Which conformation is favored?
Look at the following structure of the female hormone estrone, and tell whether each of the two indicated ring-fusions is cis or trans.

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