Chapter 18: Q42E (page 594)
Question: tert-Butyl ethers can be prepared by the reaction of an alcohol with2-methylpropene in the presence of an acid catalyst. Propose a mechanismfor this reaction
Chapter 18: Q42E (page 594)
Question: tert-Butyl ethers can be prepared by the reaction of an alcohol with2-methylpropene in the presence of an acid catalyst. Propose a mechanismfor this reaction
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Get started for freeName the following ethers:
e)
Meerweinโs reagent, triethyloxoniumtetrafluoroborate, is a powerful ethylating agent that converts alcohols into ethyl ethers at neutral pH. Show the reaction of Meerweinโs reagent with cyclohexanol, and account for the fact that trialkyloxonium salts are much more reactive alkylating agents than alkyl iodides.
Meerweinโs reagent
Predict the product(s) and provide the mechanism for each reaction below. What do the mechanisms have in common?
a.
b.
c.
d.
Aldehydes and ketones undergo acid-catalyzed reaction with alcoholsto yield hemiacetals,compounds that have one alcohol-like oxygenand one ether-like oxygen bonded to the same carbon. Further reactionof a hemiacetal with alcohol then yields an acetal,a compound that hastwo ether-like oxygens bonded to the same carbon.
(a)Show the structures of the hemiacetal and acetal you would obtainby reaction of cyclohexanone with ethanol.
(b)Propose a mechanism for the conversion of a hemiacetal into anacetal.
Predict the product(s) and provide the mechanism for each reaction below. What does each mechanism have in common?
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