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Heating an alcohol with sulfuric acid a good way to prepare a symmetrical ether such as diethyl ether. Explain why is not a good way to prepare an unsymmetrical ether such as propyl ether. Match the words in the left column to the appropriate blanks in the sentence on the right. more than half R'OH three two ROR' none ROH less than half all four To synthesize an unsymmetrical ether by this method, two different alcohols (ROH and) have to be heated with sulfuric acid. Therefore, different ethers would be obtained as products. Consequently, of the total amount of ether that is synthesized would be the desired ether.

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By using this approach, two distinct alcohols (R-O-H and R'-O-H) must be heated with sulfuric acid in order to create an unsymmetrical ether (R-O-R').

  • The hydroxyl functional group (OH) in alcohol is an organic molecule that can be linked to saturated carbon.
  • Ether is a non-reactive organic solvent for other organic compounds because of its structure, which consists of an oxygen atom forming single bonds with two additional carbon atoms.
  • Organic compounds known as ketones have an attached carbonyl group to oxygen. With oxygen, it forms double bonds RC=O

As a result, three separate ethers would be produced. As a result, less than half of the ether that is produced overall would be the desired ether.

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