Consider rotation about the indicated bond in the molecule below. Which Newman Projection formula best represents the most stable conformer of the molecule with respect to rotation about the indicated bond? [As noted below: there is no steric strain between -H and -Et that have a gauche, staggered relationship] H CH3 Br-C-C-CH₂CH3 HH H H Br CH3CH₂ 1 CH3 H CH3CH₂ H Br H₂C || H H H₂C H Br H ||| Select one: OA. I OB. II O C. III D. All conformers have identical energies. CH₂CH3 H NOTE CH3CH₂ no steric strain
Consider rotation about the indicated bond in the molecule below. Which Newman Projection formula best represents the most stable conformer of the molecule with respect to rotation about the indicated bond? [As noted below: there is no steric strain between -H and -Et that have a gauche, staggered relationship] H CH3 Br-C-C-CH₂CH3 HH H H Br CH3CH₂ 1 CH3 H CH3CH₂ H Br H₂C || H H H₂C H Br H ||| Select one: OA. I OB. II O C. III D. All conformers have identical energies. CH₂CH3 H NOTE CH3CH₂ no steric strain
Chemistry
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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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![**Rotational Stability in Newman Projections**
Consider rotation about the indicated bond in the molecule below. Which Newman Projection formula best represents the most stable conformer of the molecule with respect to rotation about the indicated bond? [As noted below: there is no steric strain between -H and -Et that have a gauche, staggered relationship]
**Diagrams:**
- There is a molecular diagram at the top showing a compound with a central carbon atom bonded to a bromine, a hydrogen, and an ethyl group (CH₂CH₃).
- Below are three Newman projection diagrams labeled I, II, and III:
- **I**: Shows bromine and an ethyl group in a staggered formation with hydrogen atoms.
- **II**: Shows bromine and hydrogen in a staggered formation with an ethyl group and other hydrogen atoms.
- **III**: Shows the ethyl group and hydrogen staggered, with bromine positioned next to hydrogen atoms.
- A note box to the right emphasizes that there is "no steric strain" when CH₃CH₂ and H are in this position.
**Select one:**
- A. I
- B. II
- C. III
- D. All conformers have identical energies.
The diagram in the note suggests that the absence of steric strain occurs when larger groups are staggered.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc14b7619-7f42-456d-bd15-e2d5f2d4f203%2F5090caff-67cc-4747-9f8f-e679c488e80d%2Fyu485ta_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Rotational Stability in Newman Projections**
Consider rotation about the indicated bond in the molecule below. Which Newman Projection formula best represents the most stable conformer of the molecule with respect to rotation about the indicated bond? [As noted below: there is no steric strain between -H and -Et that have a gauche, staggered relationship]
**Diagrams:**
- There is a molecular diagram at the top showing a compound with a central carbon atom bonded to a bromine, a hydrogen, and an ethyl group (CH₂CH₃).
- Below are three Newman projection diagrams labeled I, II, and III:
- **I**: Shows bromine and an ethyl group in a staggered formation with hydrogen atoms.
- **II**: Shows bromine and hydrogen in a staggered formation with an ethyl group and other hydrogen atoms.
- **III**: Shows the ethyl group and hydrogen staggered, with bromine positioned next to hydrogen atoms.
- A note box to the right emphasizes that there is "no steric strain" when CH₃CH₂ and H are in this position.
**Select one:**
- A. I
- B. II
- C. III
- D. All conformers have identical energies.
The diagram in the note suggests that the absence of steric strain occurs when larger groups are staggered.
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