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 freeDraw two different chair conformations of cyclohexanol (hydroxycyclohexane),showing all hydrogen atoms. Identify each position as axial orequatorial.
Name the following substances, including the cis- or trans- prefix (red-brown= Br):
Draw the two chair conformations of cis-1-chloro-2-methylcyclohexane. Which is more stable, and by how much?
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.
What do you think about this solution?
We value your feedback to improve our textbook solutions.