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. Drawing I a DrDraw 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.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. .Н T
- Please don't provide handwriting solutionDraw 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.Does the molecule below exist exist as a pair of enantiomers, as a pair of enantiomers? If so, change the bonds to wedges and dashes to reflect S stereochemistry. If the molecule does not check the box below. H CI C D x Ć G D c* e E