Write 1,2,3-trimethylcyclohexane a conformational structure for in which all the methyl groups are axial and then show its more stable conformation.

Organic Chemistry
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ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter3: Organic Compounds: Alkanes And Their Stereochemistry
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Problem 54AP: In the next chapter we'll look at cycloalkanes—saturated cyclic hydrocarbons—and we’ll see...
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Write
1,2,3-trimethylcyclohexane
a conformational structure for
in which all the
methyl groups are axial and then show its more stable
conformation.
Transcribed Image Text:Write 1,2,3-trimethylcyclohexane a conformational structure for in which all the methyl groups are axial and then show its more stable conformation.
Create a conformational analysis using the molecule in
the picture. Follow the instruction in the picture when you
transform the molecule into its Newman projection.
Explain your conformational analysis
Which conformer is the most stable? Explain.
• Which conformer is the most unstable? Explain.
Note:
Use the term angle strain, torsional strain other technical
terms when explaining.
Attachments
H
4 111
CI
Rotate C, when doing
Conformational analysis
CI
Conformational
analysis.png
H
CH3
Transcribed Image Text:Create a conformational analysis using the molecule in the picture. Follow the instruction in the picture when you transform the molecule into its Newman projection. Explain your conformational analysis Which conformer is the most stable? Explain. • Which conformer is the most unstable? Explain. Note: Use the term angle strain, torsional strain other technical terms when explaining. Attachments H 4 111 CI Rotate C, when doing Conformational analysis CI Conformational analysis.png H CH3
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