Give the correct conformation of the compound A and B. H. H. H. H. H. H. H H. H H. H. O A. s-cis and r-trans OB. Cis and trans C. r-cis and r-trans O D. s-cis and s-trans
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Q: ARO MAT TIC HYD :)0 ROC
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- Among the figure, (a) what is the most stable conformation of n-pentane? (b) gauche conformation of butane and (c) least stable conformation of butaneBuild 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.why is this the chair conformation for the cyclohexane? also is the chair conformation cis or trans
- Ethylene glycol is unusual in that the gauche conformation is more stable than the anti conformation. Offer an explanation.Is the 1st compound ( more, less or equally) stable than B? Pls show through illustrations of chair conformationsTake a look at the butane conformers below. Identify: (a)Which is an anti conformation in Newman? (b)Which is a Gauche conformation? (c)Which is the more stable Sawhorse conformer? (d)Which has the same potential energy/strain with ALS?
- Select the more stable conformation of cis‑1,2‑di(2‑methylpropyl)cyclohexane. A B C D Select the more stable conformation of trans‑1,2‑di(2‑methylpropyl)cyclohexane. A B C D Select the most stable conformation overall. A B C DExplain why butane is customarily drawn in the sawtooth conformation that it is.For the 1,2-dichlorocyclohexane stereoisomers, which conformation of the trans stereoisomer has the lower energy, the diaxial or the diequatorial conformer? Which isomer and conformation of the three you built has the lowest energy? E of all the isomers of 1,2-dichlorocyclohexane. Explain the differences in energy, i.e., identify the sources of strain in the conformations you built. Show the sources of strain in a drawing.