5. a. Draw the major product of the following reaction. NaCN Br b. Determine the absolute configuration of each chiral center in the starting material and the product. c. What was the stereochemical outcome at the reaction site? (retention or inversion) Explain. d. The same alkyl halide as in #5a was reacted with excess CH;OH. Three products were obtained, A, B and C. Products A and B are diastereomers and product Cis a constitutional isomer of A and B. Draw the three products A, B and C, clearly showing stereochemistry. e. Draw the mechanism using curved arrows to show how the three products in #5d were formed.

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Need only parts D and E answered! Thank you very much.

5. **a.** Draw the major product of the following reaction.

- The image depicts a cyclohexane ring with a wedge pointing upwards and a bromine atom attached with a wedge pointing downwards. The reaction involves the reagent NaCN and an arrow indicating formation of a product.

**b.** Determine the absolute configuration of each chiral center in the starting material and the product.

**c.** What was the stereochemical outcome at the reaction site? (retention or inversion) Explain.

**d.** The same alkyl halide as in #5a was reacted with excess CH₃OH. Three products were obtained, A, B, and C. Products A and B are diastereomers and product C is a constitutional isomer of A and B. Draw the three products A, B, and C, clearly showing stereochemistry.

**e.** Draw the mechanism using curved arrows to show how the three products in #5d were formed.
Transcribed Image Text:5. **a.** Draw the major product of the following reaction. - The image depicts a cyclohexane ring with a wedge pointing upwards and a bromine atom attached with a wedge pointing downwards. The reaction involves the reagent NaCN and an arrow indicating formation of a product. **b.** Determine the absolute configuration of each chiral center in the starting material and the product. **c.** What was the stereochemical outcome at the reaction site? (retention or inversion) Explain. **d.** The same alkyl halide as in #5a was reacted with excess CH₃OH. Three products were obtained, A, B, and C. Products A and B are diastereomers and product C is a constitutional isomer of A and B. Draw the three products A, B, and C, clearly showing stereochemistry. **e.** Draw the mechanism using curved arrows to show how the three products in #5d were formed.
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