In the drawing areas below, draw the two conformations of trans-1-bromo-4-fluorocyclohexane that are typically the most stable. Besure your drawings make it possible to distinguish between the conformations.After you've drawn the conformations, answer the question below the drawing areas.Xchair flipClick and drag to startdrawing a structure.Of the two conformations you drew above, which isthe more stable?○ leftO rightO they are equally stablecannot decide without moreinformation'oXClick and drag to startdrawing a structure.X☐ :G&

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Answered: In the drawing areas below, draw the…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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In the drawing areas below, draw the two conformations of bromocyclohexane that are typically the most stable. Be sure your drawings make it possible to distinguish between the conformations. After you've drawn the conformations, answer the question below the drawing areas. G chair flip Click and drag to start drawing a structure. Of the two conformations you drew above, which is the more stable? O left O right ◇ they are equally stable cannot decide without more information X X Click and drag to start drawing a structure. C
In the drawing areas below, draw the two conformations of trans-1 - fluoro -2-iodocyclohexane that are typically the most stable. Be sure your drawings make it possible to distinguish between the conformations. After you've drawn the conformations, answer the question below the drawing areas. PLEASE DRAW 2 STABLE CHAIR FLIPS AND CHOOSE THE MOST STABLE ONE. In the drawing areas below, draw the two conformations of trans-1-fluoro-2-iodocyclohexane that are typically the most stable. Be sure your drawings make it possible to distinguish between the conformations. After you've drawn the conformations, answer the question below the drawing areas. 口 Ö Click and drag to start drawing a a structure. 5 Of the two conformations you drew above, which is the more stable? Olaft © Rudo 口 x 5 chair flip Click and drag to start drawing a s a structure. they are equally stable cannot decide without more information x Q m W 田

Rank the conformations of n-butane with reference to its potential energy from the most stable to the least stable. Rank from the most stable to the least stable. To rank items as equivalent, overlap them.
Consider pentane, C5H12. Looking through the internal C3-C4single bond, draw thesix Newman projections (where the angle between two bonds as you look through the C3and C4bond is either 0°or 60°of the different conformations. Label the conformers/rotamers using I, II, etc. a.Which conformer is the most stable? the least stable? b.Which rotamer is the anticonformer? the gaucheconformer? c.Draw the anticonformer in saw horse projection.
5. Draw the two chair conformations ("ring filips") of trans –1- ethyl-4-methylcyclohexane to show the axial and equatorial substituents (including all hydrogens). Then determine which of the two conformations is more stable and why.
Analyze the two Newman projections and determine the relationship between the two. How would you describe the relation between conformations when they are maintained at a temperature too low to permit them to interconvert? CH3 CH3 Br. H H H H A. Identify the relationship. They are identical. They are structural isomers. They are stereoisomers. They are conformers. H H -I H Br H B. What is the relationship at low temperatures? They are identical. They are conformational diastereomers. They are structural isomers. They are conformational enantiomers.
Rank the conformations of n-butane with reference to its potential energy from the most stable to the least stable. Rank from the most stable to the least stable.To rank items as equivalent, overlap them.
Draw the most stable AND most unstable conformations of the following molecules. Briefly explain your answer. Note, for linear structures looking at rotation around the bond depicted in red. HO OH HN Br
1 F1 Q @ 2 F2 W Draw the two chair cyclohexane conformations for the compound shown below. How many substituents are axial in the less stable conformation? >> F10 #3 3 C/ "CI 00 01 02 03 A Moving to another question will save this response. 80 F3 F4 ㅎ... E S4 $ R % 5 F5 T MacBook Air F6 6 Y & 7 F7 U * 00 8 DII F8 ( 9 F9 ) 0 1 I P
In the drawing areas below, draw the two most expected stable conformations of the following molecule: Br Br Be sure your drawings make it possible to distinguish between the conformations. After you've drawn the conformations, answer the question below the drawing areas. × Click and drag to start drawing a structure. O left O right Of the two conformations you drew above, which is the more stable? chair flip O they are equally stable cannot decide without more information X Click and drag to start drawing a structure. ?
4. Which structure below represents the most stable conformation of cis-1-t-butyl-4-methylcyclohexane? A B D 5. The planar form of which ring would have bond angles close to the tetrahedral value, but is destabilized by eclipsing interactions (torsional strain)? Which of the following statements about conformations is FALSE? A) Conformations can be isolated and separated at room temperature B) Conformations are interconverted by rotation about o-bonds C) For butane the staggered anti conformation is the most stable D) For ethane the eclipsed conformation is the least stable 6. 7. Which of the following compounds has two chirality centers? .H H. H3C
Starting from the wedge-and-dash structure below, rotate the back carbon to provide the Newman projection in the most stable conformation. H₂C H (H3C) 3C H H CH3 →

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