Chapter 4: Q4-43E (page 114)
Draw the two chair conformations of trans-1-chloro-2-methylcyclohexane. Which is more stable?
Short Answer
The diequitorial conformation of trans-1-chloro-2-methylcyclohexane is more stable.
Chapter 4: Q4-43E (page 114)
Draw the two chair conformations of trans-1-chloro-2-methylcyclohexane. Which is more stable?
The diequitorial conformation of trans-1-chloro-2-methylcyclohexane is more stable.
All the tools & learning materials you need for study success - in one app.
Get started for freeThe following cyclohexane derivative has three red, green, and blue substituents. Identify each substituent as axial or equatorial, and identify each pair of relationships (red–blue, red-green, and blue-green) as cis or trans.
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?
Question:There are two different substances named trans-1,2-dimethylcyclopentane. What is the relationship between them?
Draw three isomers of trans-1, 2-dichlorocyclobutane, and label them as either constitutional isomers or stereoisomers.
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?
What do you think about this solution?
We value your feedback to improve our textbook solutions.