. Name this ether correctly. CH3CH2CH2CH2-O-CHCH=CHCH3 ČH3

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 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.
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
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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