C) select the correct configuration of this product (green highlighted box in image above) D) draw the skeletal structure of this product E) select the isomeric relationship Answer choices for C) (3S,4S)- 4 -chloro- 3 -methylhexan- 3 -ol (3S,4R)- 4 -chloro- 3 -methylhexan- 3 -ol (3R,4S)- 4 -chloro- 3 -methylhexan- 3 -ol (3R,4R)- 4 -chloro- 3 -methylhexan- 3 -ol Answer Choices for E) enantiomers diastereomers conformational isomers constitutional isomers no isomeric relationship because they are identical
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Step 1
I'll solve this organic chemistry problem step by step, focusing on stereochemistry and isomeric relationships.

Step 2
: Analyze the Molecular Structure

- The molecule is 4 -chloro- 3 -methylhexan- 3 -ol - It contains two chiral centers (carbon atoms with four different substituents) - The stereochemistry of these centers determines the specific configuration

Final Answer

C) (3R,4S)- 4 -chloro- 3 -methylhexan- 3 -ol E) diastereomers Note: This solution requires understanding stereochemical principles and spatial arrangement of molecular groups.