2. a) Draw the most stable chair conformation of cis 1-isobutyl-2-methylcyclohexane. b) Draw a Newman projection of the best conformation of 2,3-difluorobutane looking down the C2-C3 bond.

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2. a) Draw the most stable chair conformation of cis 1-isobutyl-2-methylcyclohexane.
b) Draw a Newman projection of the best conformation of 2,3-difluorobutane
looking down the C2-C3 bond.
3. Compound X has the formula C46H90O4.
Compound X reacts with excess H2/Pd to give C46H9204.
How many rings does compound X have? Show how you got your answer.
4. For each pair state whether the two are a) the same molecule, b) different
compounds that are not isomers, c) constitutional isomers, d) diastereomers, or
e) enantiomers.
A)
B)
ÇH3
CH3
Br
Br
HS
CI
CI-
SH
H
Br
Br
CH3
CH3
Transcribed Image Text:2. a) Draw the most stable chair conformation of cis 1-isobutyl-2-methylcyclohexane. b) Draw a Newman projection of the best conformation of 2,3-difluorobutane looking down the C2-C3 bond. 3. Compound X has the formula C46H90O4. Compound X reacts with excess H2/Pd to give C46H9204. How many rings does compound X have? Show how you got your answer. 4. For each pair state whether the two are a) the same molecule, b) different compounds that are not isomers, c) constitutional isomers, d) diastereomers, or e) enantiomers. A) B) ÇH3 CH3 Br Br HS CI CI- SH H Br Br CH3 CH3
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