A student wanted to prepare (1-Ethylpropoxy)cyclopentane by heating cyclopentanol and pentan-3-ol under acidic conditions. On carrying out the reaction, however, she found that there were three ethers produced, each containing 10 carbon atoms. One of the ethers was (1-Ethylpropoxy)cyclopentane. Draw the structures of the other two ethers, and draw the complete, detailed mechanisms showing how all three ethers are produced. (1-Ethylpropoxy)cyclopentane
A student wanted to prepare (1-Ethylpropoxy)cyclopentane by heating cyclopentanol and pentan-3-ol under acidic conditions. On carrying out the reaction, however, she found that there were three ethers produced, each containing 10 carbon atoms. One of the ethers was (1-Ethylpropoxy)cyclopentane. Draw the structures of the other two ethers, and draw the complete, detailed mechanisms showing how all three ethers are produced. (1-Ethylpropoxy)cyclopentane
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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(SYN) The reaction in Problem 10.48 produces a mixture of ethers rather than the desired ether exclusively. Starting with the same two alcohols given in Problem 10.48, show the sequence of reactions that would need to be carried out to produce (1-Ethylpropoxy)cyclopentane as the exclusive ether
Transcribed Image Text:A student wanted to prepare (1-Ethylpropoxy)cyclopentane
by heating cyclopentanol and pentan-3-ol under acidic
conditions. On carrying out the reaction, however, she
found that there were three ethers produced, each
containing 10 carbon atoms. One of the ethers was
(1-Ethylpropoxy)cyclopentane. Draw the structures of the
other two ethers, and draw the complete, detailed
mechanisms showing how all three ethers are produced.
(1-Ethylpropoxy)cyclopentane
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