Draw the Newman Projections with the highest and lowest energy conformers for the molewkes of the below. Sight along the bond highlighted Carbons. a) Cl - CH₂ - CH₂ - Br b) CHÍCH - CHÍ CH3 F C) In the molewles above, explain why the the highest energy. conformer you drew is

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Chapter1: Chemical Foundations
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**Organic Chemistry Task: Analyzing Newman Projections**

**Objective:** Draw the Newman Projections with the highest and lowest energy conformers for the molecules below. Focus on the bond of the highlighted carbons.

**a)** Molecule: Cl-CH₂-CH₂-Br

**b)** Molecule: CH₃-CH-CH₂-CH₃  
                                 F

**c)** Explanation Required: For the molecules above, explain why the conformer you draw is the highest energy.

Note: To complete this task, use Newman projections to clearly visualize the spatial arrangement and energy levels. Highlight steric hindrance and electron interactions to justify energy distinctions.
Transcribed Image Text:**Organic Chemistry Task: Analyzing Newman Projections** **Objective:** Draw the Newman Projections with the highest and lowest energy conformers for the molecules below. Focus on the bond of the highlighted carbons. **a)** Molecule: Cl-CH₂-CH₂-Br **b)** Molecule: CH₃-CH-CH₂-CH₃                       F **c)** Explanation Required: For the molecules above, explain why the conformer you draw is the highest energy. Note: To complete this task, use Newman projections to clearly visualize the spatial arrangement and energy levels. Highlight steric hindrance and electron interactions to justify energy distinctions.
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Step 1: Interpretation of given problem

Given are organic compounds.

In Newman projections, eclipsed conformation is highest energy conformation and staggered conformation is lowest energy conformation 

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