Translate the given conformer from the wedge-and-dash drawing into its Newman projection. You might find it helpful to make amodel, then manipulate it to the desired viewpoint.H3CH.Clil.BrCH3Which Newman structure matches the conformer? Which Newman structure matches the conformer?CH3H CH3H.CH3CH3BrCIBrH.BrHCH3-CH3CH3CICH3H.BrCI

Answered: Image /qna-images/answer/8f453ade-b808-4336-be74-0404ac051915.jpg

Answered: Translate the given conformer from the…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 4E: Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This...

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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.
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.
a model of cyclohexane in a chair conformation, and explain why the names “axial” and“equatorial’ are appropriate.
draw the newman projection looking down the indicated bond, and then draw the most stable and least stable conformation...
Observe the Newman projection of the next molecule along the bond shown in red with the front carbon the one bonded to "Cl". a) Draw one of the Newman projections of the molecule with a staggered conformation. b) Draw one of the Newman projections of the molecule with an eclipsed conformation.
Draw both a chair confirmation of the substitutes cyclohexane drawn below. Be certain to actually do a ring flip. Also be certain to very clearly distinguish axial from equatorial positions. Then circle the more stable conformation.
How many alkyl substituents are axial in the lowest energy conformation?
Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed down the red bond in the direction of the red arrow. Your projection should be oriented as shown by the arrow marked up. So the CH2SH group on the front carbon should be above the H and H3C groups, no matter which template you use
Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed down the red bond.
Newman projection, and conformer of
Imagine that this worksheet has sucked you the plane of the page, and you are now facing the indicated bond of the drawn molecule. a. Draw the six main Newman projections for the indicated bond: three eclipsed, three staggered. b. Label which conformers are eclipsed ands taggered.c. Identify the most and least stable conformer, and explain your reasoning.
Draw both trans chair conformations of 2-methylcyclohexanol and circle the more stable one.

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Translate the given conformer from the wedge-and-dash drawing into its Newman projection. You might find it helpful to make a model, then manipulate it to the desired viewpoint. H3C H. Cli.. Br CH3 Which Newman structure matches the conformer?