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d) [RX] is halved, and [:Nu-] is doubled. • Question 4: (a) Draw the product (including stereochemistry) of the following SN2 reaction. CH3 H Br + CN H

d) [RX] is halved, and [:Nu-] is doubled. • Question 4: (a) Draw the product (including stereochemistry) of the following SN2 reaction. CH3 H Br + CN H

Chemistry
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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Transcription of the image content for educational purposes: --- **Question 4:** (a) Draw the product (including stereochemistry) of the following SN2 reaction. Structure: A cyclohexane ring with a bromine (Br) atom on the first carbon and a methyl (CH₃) group on the adjacent carbon. + CN⁻ Diagram explanation: The CN⁻ (cyanide ion) is shown as an attacking nucleophile in the SN2 reaction, depicted with an arrow indicating the substitution of the bromine atom. **Question 5:** Draw the products of each SN1 reaction and indicate the stereochemistry of any stereogenic centers. --- The content includes questions regarding SN2 and SN1 reactions, focusing on drawing reaction products and considering stereochemistry changes.
Transcribed Image Text:Transcription of the image content for educational purposes: --- **Question 4:** (a) Draw the product (including stereochemistry) of the following SN2 reaction. Structure: A cyclohexane ring with a bromine (Br) atom on the first carbon and a methyl (CH₃) group on the adjacent carbon. + CN⁻ Diagram explanation: The CN⁻ (cyanide ion) is shown as an attacking nucleophile in the SN2 reaction, depicted with an arrow indicating the substitution of the bromine atom. **Question 5:** Draw the products of each SN1 reaction and indicate the stereochemistry of any stereogenic centers. --- The content includes questions regarding SN2 and SN1 reactions, focusing on drawing reaction products and considering stereochemistry changes.
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