In the drawing areas below, draw the two conformations of bromocyclohexane that are typically the most stable. Be sure yourdrawings make it possible to distinguish between the conformations.After you've drawn the conformations, answer the question below the drawing areas.Gchair flipClick and drag to startdrawing a structure.Of the two conformations you drew above, which isthe more stable?O leftO right◇ they are equally stablecannot decide without moreinformationXXClick and drag to startdrawing a structure.C

Step 1:Cyclohexane in reality is in puckered form which is called "chair form" because it is most…

Answered: In the drawing areas below, draw the…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter3: Organic Compounds: Alkanes And Their Stereochemistry

Section3.SE: Something Extra

Problem 52AP: Increased substitution around a bond leads to increased strain. Take the four substituted butanes...

See similar textbooks

Similar questions

Increased substitution around a bond leads to increased strain. Take the four substituted butanes listed below, for example. For each compound, sight along the C2-C3 bond and draw Newman projections of the most stable and least stable conformations. Use the data in Table 3-5 to assign strain-energy values to each conformation. Which of the eight conformations is most strained? Which is least strained? (a) 2-Methylbutane (b) 2,2-Dimethylbutane (c) 2,3-Dimethylbutane (d) 2,2,3-Trimethylbutane
In the drawing areas below, draw the two conformations of trans-1-bromo-4-fluorocyclohexane 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. X chair flip Click and drag to start drawing a structure. Of the two conformations you drew above, which is the more stable? ○ left O right O they are equally stable cannot decide without more information 'o X Click and drag to start drawing a structure. X ☐ : G &
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.
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. ?
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.
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.
Rank these conformations from least to most stable (less stable < more stable). H. CH3 H3C. H3C CYH `H. H. H3C H H3C ČH3 II II O 1. I| < III
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
Identify the correct chair conformations of the following compound and then indicate which one is more stable. OH OH OH HO 1 || 4 OI and II are correct chair structures and I is most stable OI and II are correct chair structures and II is most stable OI and III are correct chair structures and III is most stable O II and III are correct chair structures and II is most stable O II and III are correct chair structures and III is most stable |||
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
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.
Which is the least stable molecule of the 5 shown? Does the least stable molecule have steric strain??

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry
Chemistry
ISBN:
9781305080485
Author:
John E. McMurry
Publisher:
Cengage Learning

SEE MORE TEXTBOOKS