1. Draw the correct skeletal structure of 4,4-dibromo-1-butanol: ; draw its most stable conformer looking along C2-C3 the Newman projection to differentiate them from methyl groups and draw all the carbons skeletal and on the Newman Projection provided Draw the hydrogens that are directly connected to draw the corect skeletal structure here

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Chapter1: Chemical Foundations
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1. **4,4-dibromo-1-butanol: Skeletal Structure and Newman Projection**

   - **Instructions**: Draw the skeletal structure of 4,4-dibromo-1-butanol. Use the provided Newman Projection template to visualize the most stable conformation when looking along the C2-C3 bond. Indicate the hydrogens that are directly connected to the Newman projection, and differentiate them from the methyl groups. Ensure all carbon atoms are drawn in the skeletal structure.
   
   - **Diagram**: The figure on the right displays a Newman projection view of a carbon-carbon bond with substituents arranged around it.

2. **1R, 2S, 4R-4-tert-butyl-1-ethyl-2-methylcyclohexane: Skeletal Structure and Conformations**

   - **Instructions**: Draw the skeletal structure of the molecule. Depict its most stable conformer by initially highlighting the hydrogens attached directly to the cyclohexane ring. In the final structure, omit the hydrogens while accurately representing the three alkyl groups in skeletal form. Ensure consistent bond lengths.

   - **Diagrams**:

     - **First Diagram**: A numbered cyclohexane ring indicating where to draw the skeletal structure, showcasing stereochemistry.
     - **Second Diagram**: A chair conformation of the cyclohexane with labeled substituents includes hydrogens attached to the ring.
     - **Third Diagram**: A simplified version of the chair conformation illustrating only the alkyl groups, with uniform bond lengths.
Transcribed Image Text:1. **4,4-dibromo-1-butanol: Skeletal Structure and Newman Projection** - **Instructions**: Draw the skeletal structure of 4,4-dibromo-1-butanol. Use the provided Newman Projection template to visualize the most stable conformation when looking along the C2-C3 bond. Indicate the hydrogens that are directly connected to the Newman projection, and differentiate them from the methyl groups. Ensure all carbon atoms are drawn in the skeletal structure. - **Diagram**: The figure on the right displays a Newman projection view of a carbon-carbon bond with substituents arranged around it. 2. **1R, 2S, 4R-4-tert-butyl-1-ethyl-2-methylcyclohexane: Skeletal Structure and Conformations** - **Instructions**: Draw the skeletal structure of the molecule. Depict its most stable conformer by initially highlighting the hydrogens attached directly to the cyclohexane ring. In the final structure, omit the hydrogens while accurately representing the three alkyl groups in skeletal form. Ensure consistent bond lengths. - **Diagrams**: - **First Diagram**: A numbered cyclohexane ring indicating where to draw the skeletal structure, showcasing stereochemistry. - **Second Diagram**: A chair conformation of the cyclohexane with labeled substituents includes hydrogens attached to the ring. - **Third Diagram**: A simplified version of the chair conformation illustrating only the alkyl groups, with uniform bond lengths.
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