Determine the name of the compound based on the Newman projections shown below. CH₂CH₂ H H H . H H₂CH₂C 5 CH, П H H CH3 H Н H H H H CH C V "I CH₂ CH3 CH₂CH3 H H H Н Н IV Ш H Н CH3 0 H CH₂CH3 CH3 CH₂CH3 Н H
Determine the name of the compound based on the Newman projections shown below. CH₂CH₂ H H H . H H₂CH₂C 5 CH, П H H CH3 H Н H H H H CH C V "I CH₂ CH3 CH₂CH3 H H H Н Н IV Ш H Н CH3 0 H CH₂CH3 CH3 CH₂CH3 Н H
Chemistry
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
Transcribed Image Text:**Understanding Newman Projections in Organic Chemistry**
Newman projections are useful tools for visualizing the conformational structure of molecules, specifically for looking down the bond between two carbon atoms. Below are several Newman projections that depict the conformations of a particular compound.
**Determine the name of the compound based on the Newman projections shown below.**
***Figure Breakdown:***
1. **Projection I**
- Front carbon: Hydrogens at the 2 and 4 o'clock positions.
- Back carbon: Ethyl group (CH2CH3) at the 12 o'clock position, methyl group (CH3) at the 6 o'clock position, hydrogens at 2 and 4 o'clock positions.
2. **Projection II**
- Front carbon: All hydrogens at 12, 2, and 4 o'clock positions.
- Back carbon: Ethyl group (CH2CH3) at the 4 o'clock position, methyl group (CH3) at the 6 o'clock position, hydrogen at the 12 o'clock position.
3. **Projection III**
- Front carbon: Hydrogens at 12, 2, and 4 o'clock positions.
- Back carbon: Ethyl group (CH2CH3) at the 4 o'clock position, methyl group (CH3) at the 6 o'clock position, hydrogen at 12 o'clock position.
4. **Projection IV**
- Front carbon: Hydrogen at the 10, 2, and 4 o'clock positions.
- Back carbon: Ethyl group (CH3CH2) at the 6 o'clock position, methyl group (CH3) at the 4 o'clock position.
5. **Projection V**
- Front carbon: Hydrogens at 12, 2, and 4 o'clock positions.
- Back carbon: Ethyl group (CH3CH2) at 4 o'clock position, methyl group (CH3) at 6 o'clock position, hydrogen at 12 o'clock position.
6. **Projection VI**
- Front carbon: Hydrogen at the 10, 2, and 4 o'clock positions.
- Back carbon: Ethyl group (CH3CH2) at 4 o'clock position, methyl group (CH3) at 6 o'clock position.
Each projection offers a unique rotational perspective along the carbon-carbon bond of the
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