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2 cards from this section. Quick, good the night before a test.
What is the general structure of ethers?
Think about the components that make up ethers.
What is the order of reactivity for ether cleavage with hydrogen halides?
Focus on the strength of the acids involved.
Which of the following hydrogen halides is the most effective for cleaving ethers?
Consider which is stronger based on their acidic properties.
True or False: Ethers are more reactive than alcohols.
Think about the conditions needed for each to react.
Devise a synthetic route to produce anisole from phenol. Consider the necessary reagents and steps.
Identify the electrophilic substitution reaction that occurs.
How would one prepare triethyl ether using the Williamson synthesis? Name all reagents and conditions required.
Focus on ensuring the use of an unhindered alkyl halide.
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