Which of the following best explains the reason for the relative stabilities of the conformersshown?II.H3C CH3I.HCH3...-H--H.H3CHA I has more steric strain.B Il has more torsional strain.I has more torsional strain.D II has more steric strain.

Strain cause by the repulsion of electrons in bonds . I is eclipsed conformation but anti-clinal…

ch of the following best explains the reason for the relative stabilities of the conformers vn? II. H3C CH3 I. CH3 ... -H H H3C H. H I has more steric strain. Il has more torsional strain. I has more torsional strain. Il has more steric strain.

ch of the following best explains the reason for the relative stabilities of the conformers vn? II. H3C CH3 I. CH3 ... -H H H3C H. H I has more steric strain. Il has more torsional strain. I has more torsional strain. Il has more steric strain.

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...

See similar textbooks

Related questions

Q: 4 - 8. Provide the lowest energy conformation for each of the following: 4. d.) a.) b.) c.) D c.)…

A: Lowest energy conformation of substituted cyclohexane is the one which has most stable chair…

Q: Which chair conformer is the most stable/lower in energy: EXY Because axial positions are more…

A: Given chair conformations:

Q: Which of the following is a Newman projection for the following compound as viewed down the…

A: This is a simple problem of stereochemistry where we have to fin the Newman projection from zig-zag…

Q: draw Newman projection of the conformer by looking C1-C2 and C4-C

A: Newman projection is studied along the carbon-carbon axis and two carbon atoms are represented by a…

Q: Which of the following two conformers is higher in potential energy? H₂CH H CH₂ | H CH₂ Select one:…

A: Here, we have to find the conformer that is higher in potential energy.

Q: For the molecule shown below, draw both chair conformations and circle which is the lower energy…

A: The given molecule is (1S,2S,4S)-1,2,4-trifluorocyclohexane. It contains three fluorine group…

Q: 4. a. Draw the two chair conformations for cis-1,4-dimethylcyclohexane. Use the given template. In…

A: We have to complete the structural form and choose the correct option.

Q: Which is the lowest energy conformer of 2-methylbutane? A) C) H₂C O 1. A O 4. D O 2. B H₂C. $ O 3. C…

A: Given in following 2-methylbutane conformers which have lowest energy means stability is more…

Q: dentify the conformer with the highest energy. CH₂ Oa. D O b. E. 0 c. C d. A e. B D H

A: -> Conformers refers to different spatial arrangements of atoms in a molecule that results from…

Q: Identify the most stable conformer: CH2CH3 CH2CH3 H. H. H. `H CH2CH3 ČH3 II ČH3 II H. H. H. H3CH2C.…

A: Newman projection formula is a way of representing molecules. In this confirmation, the chemical…

Q: 1) Are the molecules A and B... conformational isomers? Diastereomers? Enantiomers? Position…

A: The enantiomers are the compounds that are mirror images of each other but are not superimposable.…

Q: 6. Consider the following Newman Projections. Which is the most stable conformation? Which is the…

Q: Which is the lowest energy conformer of 2-methylbutane? A) C) O 1. A 04. D O 2. B O 3. C B) H₂C. 安安…

Q: Which statement is true about these conformers? H H H H. CH3 -- H3C TH. H,C H,C H. H A B.

A: Given:

Q: g. Draw two chair conformations of the following molecule and indicate which one is more stable. h.…

A: Here we have to write the chair conformation and predict the most stable conformation of the…

Q: [Review Topics) [References) Specify the types of strain that destabilize the conformer shown below.…

A: Torsional strain is generated when two groups are placed at 1 and 3 positions with respect to…

Q: NH₂ 8 A. NH2 NH₂ B. H3C CH3 CH3 C. H3C,,. ... OH CH3 H₂N. D. H₂N NH₂ NH₂

A: Chair conformation: A six-membered ring configuration in which the planes shared by atoms 2, 3, 5,…

Q: None

A: Answer image:When drawing the chair conformers for a cyclohexane derivative, the groups that are…

Q: ecify the types of strain that destabilize the conformer shown below. Hint: All bonds not explicitly…

A: Torsional strain is the strain between the bonding electrons of two nearest bonds those don't shear…

Q: 13a. Draw the correct skeletal structure of 5-methyl-1-hexanol. provided (13b.) draw in skeletal…

A: a.) Skeletal Structure of a compound is drawn by using IUPAC rules . We need to check the carbon…

Q: . Draw the chair conformers of each of the following cyclohexane. 2. which one is more stable in…

Q: 1. Classify the following compounds as constitutional isomers, conformations, enantiomers,…

A: Answer : 1) meso compound 2) Enantiomers 3) conformation isomers 4) constitutional isomers…

Q: 4. Draw the Newman projection of the conformer below as it is drawn looking down the indicated C-C…

A: Newmann projections.

Q: ✔ Preview File Edit View Go Tools Window Help Q Search U2HW5.pdf Page 1 of 2 372 U2HW5.pdf H CH3…

A: Give many confirmation of isomers select most stable and least stable .

Q: O Which is the most stable chair conformer of the following compound? EM NH NH NH₂ D. A. B. A D B C.

A: -> chair conformer must have same molecular formula to given compound . -> conformer is most…

Q: CH2CH2CH3 CH2CH2CH3 CH2CH2CH3 CH2CH2CH3 F CH2CH2CH3 CH2CH3 H. H CH2CH3 H3CH2C- H. F- H' H H. H…

Q: Indicate the position, axial or equatorial, of each of the groups shown when the ring is in its more…

A: The basic principle is; the bulky group (in this case isopropyl) should always come at equatorial…

Q: Rank these conformations from Teast to most Stable lless c more stably H CH3 Hj C HgC CH3 H. HgC

Q: - Which conformation of cyclohexane experiences the most transannular strain? a. chair b. planar c.…

Q: 6. Draw the two chair conformations of the molecule below. Which is the most stable? HO

Question

Which of the following best explains the reason for the relative stabilities of the conformers
shown?
II.
H3C CH3
I.
H
CH3
...
-H
--
H.
H3C
H
A I has more steric strain.
B Il has more torsional strain.
I has more torsional strain.
D II has more steric strain.

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps

SEE SOLUTION Check out a sample Q&A here

Similar questions

Consider the energy diagram showing the conformational analysis of propane and match the indicated position with the correct conformation below. 00000 - = 3 2 OIV OV Н. CH3 Н Н H пи m 0 dihedral angle energy 180 HH H Н II Н. H Н Ш CH3 H 180 HCH3 HXH Н IV HCH3 CH3 HXH Н V
Draw the following molecules in their most stable conformation. You do not have to draw the least stable conformation, unless you find it helpful practice.
6. Sort the following conformations of 1-chloropropane from most stable to least stable. H CI Hн Н Н Н CH₂ н H н CI 2) Н CH, H 3) CH1 CI
Which statement describes the conformations below? H₂CCI I H. H CI CH3 'Н H The staggered conformation on the left is more stable. O The staggered conformation on the right is more stable. The eclipsed conformation on the left is more stable. The eclipsed conformation on the right is more stable.
9. Draw the two chair conformations of the following molecule. Describe spatial relationship of the two chlorine atoms as gauche, anti or eclipsed? CI CI
Decide which conformation in each pair of compounds is more stable