Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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What will be the correct stereochemistry of the product?

Transcribed Image Text:**Reaction Description:**
- **Question:** What will be the correct stereochemistry of the product of this reaction?
- **Reaction Details:**
- The starting material is a cyclohexane ring with a bromine (Br) substituent.
- The bromine is on a wedge, indicating it is positioned above the plane of the ring.
- The reaction conditions include sodium cyanide (NaCN).
**Explanation:**
This reaction likely involves a nucleophilic substitution, where the NaCN acts as a nucleophile and replaces the bromine atom. The resulting product may show inversion of configuration due to the typical SN2 reaction mechanism, which means if the bromine was wedge (above the plane), the CN group would then be on a dash (below the plane).
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