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
![**Question 4:**
Name this ether correctly.
\[ \text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_2\text{-O-CH(CH}_3\text{)CH=CHCH}_3 \]
**Question 5:**
Show the best way to make the ether in Problem #4, using a Williamson Ether Synthesis, starting from an alcohol/phenol.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F60a763da-0d80-48cc-b9af-a1764b06c188%2F1e5ed5f8-7699-4354-9f77-674153a569f4%2Fy4vs6ev_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Question 4:**
Name this ether correctly.
\[ \text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_2\text{-O-CH(CH}_3\text{)CH=CHCH}_3 \]
**Question 5:**
Show the best way to make the ether in Problem #4, using a Williamson Ether Synthesis, starting from an alcohol/phenol.
Expert Solution
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Step 1 Introduction
IUPAC rules :
Ethers name should be "alkoxyalkane" , lower carbons chain should be alkoxy side , where as higher carbon chain as parent chain
Williomson's etherification :
alkylhalide reacts with alkoxide ion to give ether as major product via SN2 mechanism . It is an example for nucleophilic substitution reaction
primary alkylhalides are more preforable while preparing ether, if we use secondary (or) tertiary alkyl halides elimination product is formed instead of substitution reaction
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