**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.

pTsCl stands for p-toluenesulfonyl chloride and N(CH2CH3)3 act as a base.Treatment of alcohol with…

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

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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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.

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