Draw one of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Q
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- Indicate the relationship between each pair. Choose from: configurational stereoisomers,conformers, constitutional isomers, or different formulas (Each term is used at least twice.)Build a model of methylcyclohexane, and use the model to complete the following Newmanprojections of methylcyclohexane in the chair conformation: a. When the methyl group is in an axial or equatorial (circle one) position, the molecule is inits lowest potential energy conformation. b. Label one Newman projection above anti and the other gauche to describe the relationshipbetween the methyl group and C3 of the ring. c. In general, which is a lower PE conformation, anti or gauche? d. Explain how your answer to b and c provide an explanation for why it is more favorable fora large group to be in an equatorial than an axial position.Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.
- Draw one of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. CIDraw one of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. .Н TDraw one of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. SH Drawing
- Draw one of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. HO Draw a DiastereomerDraw both of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.Draw one of the possible diastereomers of the molecule shown below. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Drawing &
- What's the stablest conformation Newmann projection for this molecule looking down the C3-C4 bond?The molecule (I) and (II) are || CH3 **H I Identical Enantiomers Diastereomers Constitutional Isomers Next H3C X IIto Medical Chemistry II. (BMC1CHEM02) oard / My courses / Introduction to Medical Chemistry II. (BMCICHEM02) / 29/03 2021 Chemistry Electronic te Electronic test in Chemistry n3 Cyclobutane is more stable molecule than cyclopropane, because.... Select one: ut of it has less angle strain. cyclobutane has a cis-trans stereoisomers. cyclobutane is a larger ring. it has more torsional strain. cyclopropane is planar. Next page