Identify the best conditions to complete the SN2 reaction shown below. .CI A) NaN, DMSO B) NaCN, ETOH C) NaCN, acetonitrile D) NANH2, acetonitrile CN E) LICI, THF

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...
icon
Related questions
Question
100%
**Identify the best conditions to complete the SN2 reaction shown below.**

**Diagram Description:**

The diagram depicts a chemical reaction involving a substitution process. The starting molecule is a linear alkyl halide, specifically a pentyl chloride, where a chlorine (Cl) atom is attached to the carbon chain. An arrow points from this molecule to a product where the chlorine has been replaced by a cyano group (CN), indicating that a nucleophilic substitution (SN2) reaction has occurred.

**Answer Choices:**

A) NaN, DMSO  
B) NaCN, EtOH  
C) NaCN, acetonitrile  
D) NaNH₂, acetonitrile  
E) LiCl, THF

**Explanation:**

In an SN2 reaction, a strong nucleophile and a polar aprotic solvent are usually preferred to facilitate the substitution process. The reaction involves the direct attack by the nucleophile on the substrate, resulting in a one-step mechanism where the leaving group is displaced.
Transcribed Image Text:**Identify the best conditions to complete the SN2 reaction shown below.** **Diagram Description:** The diagram depicts a chemical reaction involving a substitution process. The starting molecule is a linear alkyl halide, specifically a pentyl chloride, where a chlorine (Cl) atom is attached to the carbon chain. An arrow points from this molecule to a product where the chlorine has been replaced by a cyano group (CN), indicating that a nucleophilic substitution (SN2) reaction has occurred. **Answer Choices:** A) NaN, DMSO B) NaCN, EtOH C) NaCN, acetonitrile D) NaNH₂, acetonitrile E) LiCl, THF **Explanation:** In an SN2 reaction, a strong nucleophile and a polar aprotic solvent are usually preferred to facilitate the substitution process. The reaction involves the direct attack by the nucleophile on the substrate, resulting in a one-step mechanism where the leaving group is displaced.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 1 images

Blurred answer
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY