Homework Help is Here – Start Your Trial Now!
Science
Chemistry
← Problem 18 of 24 Submit Draw the product of the reaction shown below. Ignore inorganic byproducts.

← Problem 18 of 24 Submit Draw the product of the reaction shown below. Ignore inorganic byproducts.

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...
See similar textbooks
icon
Related questions
Question
**Problem 18 of 24** **Instruction:** Draw the product of the reaction shown below. Ignore inorganic byproducts. **Reaction Information:** - **Starting Material:** The structure is a cyclopentane ring attached to a straight chain terminating with an OH group. - **Reagents:** - pTsCl (p-Toluenesulfonyl chloride) - N(CH₂CH₃)₃ (Triethylamine) **Explanation:** The starting compound is a cyclopentane with an alcohol (-OH) functional group. The reagents mentioned indicate a typical transformation where the -OH group is converted into a tosylate group using p-Toluenesulfonyl chloride (pTsCl) in the presence of a base, such as triethylamine (N(CH₂CH₃)₃). This reaction often replaces the -OH group with a tosyl group (-OTs), making the compound suitable for further reactions, such as nucleophilic substitutions or eliminations.
Transcribed Image Text:**Problem 18 of 24** **Instruction:** Draw the product of the reaction shown below. Ignore inorganic byproducts. **Reaction Information:** - **Starting Material:** The structure is a cyclopentane ring attached to a straight chain terminating with an OH group. - **Reagents:** - pTsCl (p-Toluenesulfonyl chloride) - N(CH₂CH₃)₃ (Triethylamine) **Explanation:** The starting compound is a cyclopentane with an alcohol (-OH) functional group. The reagents mentioned indicate a typical transformation where the -OH group is converted into a tosylate group using p-Toluenesulfonyl chloride (pTsCl) in the presence of a base, such as triethylamine (N(CH₂CH₃)₃). This reaction often replaces the -OH group with a tosyl group (-OTs), making the compound suitable for further reactions, such as nucleophilic substitutions or eliminations.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 3 steps with 1 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Carboxylic Acids and their Derivatives
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
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
SEE MORE TEXTBOOKS