9. Draw the chair conformation and the ring-flipped chair conformation for the following molecule. Draw Newman projections of each conformer, viewing along the C1-C6 and C3-C4 axes. Which conformation is more stable? Why?
10. Indicate the gauche interactions that each methyl group experiences with the cyclohexane ring by drawing Newman projections.
11. Place an asterisk next to each stereogenic center in cholesterol.
12. Label each molecule as chiral, achiral, or achiral/meso. Label each stereocenter as R or S.
13. Indicate if the pair of molecules are enantiomers, diastereomers, or the same molecule.
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