Determine the name of the compound based on the Newman projections shown below. CH2CH3 CH2CH3 H H. H. CH2CH3 ČH3 II CH3 II ČH3 1 H. H H. H. H3CH2C H3CH;C H. H ČH;CH3 ČH3 VI IV ČH3 V ČH3

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### Determining the Name of a Compound Using Newman Projections

Newman projections are a way of visualizing the conformation of a molecule, especially around its carbon-carbon bonds, by looking straight down the bond between two carbon atoms. Below are a series of Newman projections for a particular compound. We aim to determine the name of the compound based on these projections.

#### Newman Projections:

1. **Projection I:** 
   - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation.
   - Back carbon: three hydrogens (H).
     
2. **Projection II:**
   - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation.
   - Back carbon: three hydrogens (H).

3. **Projection III:**
   - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation.
   - Back carbon: three hydrogens (H).

4. **Projection IV:**
   - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation.
   - Back carbon: three hydrogens (H).

5. **Projection V:**
   - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation.
   - Back carbon: three hydrogens (H).

6. **Projection VI:**
   - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation.
   - Back carbon: three hydrogens (H).

#### Brief Analysis:

All the Newman projections shown are staggered conformations of the same molecule, typically representing the lowest energy form.

#### Conclusion:

From the Newman projections, we can infer that the compound is **butane (C₄H₁₀)**. It is the simplest compound that fits the pattern of displaying Newman projections shown, specifically focusing on rotations and interactions around the carbon-carbon single bonds. 

Therefore
Transcribed Image Text:### Determining the Name of a Compound Using Newman Projections Newman projections are a way of visualizing the conformation of a molecule, especially around its carbon-carbon bonds, by looking straight down the bond between two carbon atoms. Below are a series of Newman projections for a particular compound. We aim to determine the name of the compound based on these projections. #### Newman Projections: 1. **Projection I:** - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation. - Back carbon: three hydrogens (H). 2. **Projection II:** - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation. - Back carbon: three hydrogens (H). 3. **Projection III:** - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation. - Back carbon: three hydrogens (H). 4. **Projection IV:** - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation. - Back carbon: three hydrogens (H). 5. **Projection V:** - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation. - Back carbon: three hydrogens (H). 6. **Projection VI:** - Front carbon: one hydrogen (H), one methyl (CH₃) group, one ethyl (CH₂CH₃) group in a staggered conformation. - Back carbon: three hydrogens (H). #### Brief Analysis: All the Newman projections shown are staggered conformations of the same molecule, typically representing the lowest energy form. #### Conclusion: From the Newman projections, we can infer that the compound is **butane (C₄H₁₀)**. It is the simplest compound that fits the pattern of displaying Newman projections shown, specifically focusing on rotations and interactions around the carbon-carbon single bonds. Therefore
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