Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Chapter 13, Problem 52P

Mixing furan (Problem 13.44) with maleic anhydride in diethyl ether yields a crystalline solid with a melting point of 125°C. When melting of this compound takes place, however, one can notice that the melt evolves a gas. If the melt is allowed to resolidify, one finds that it no longer melts at 125°C but instead it melts at 56°C. Consult an appropriate chemistry handbook and provide an explanation for what is taking place.

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A task is assigned to an undergraduate student to test two samples (known as compounds K and L) in the laboratory. She placed these two compounds through various scientific tests. She discovered that these compounds have the same molecular formula, CSHSO. When treated with 2,4-dinitrophenylhydrazine, all of these compounds produce brightly coloured precipitate, and both are reduced to an organic compound with the molecular formula C§H100. However, compound K can be easily oxidized by chromic acid to formed compound N and vice versa for compound L. Furthermore, when both compounds react with Fehling's solutions, they produce negative results. However, only compound K forms a silver mirror when it reacts with Tollen's reagent, and compound L does not. Identify the possible structural formulae for compounds K, L, and N by ignoring their position isomerism. Indicate the formation of compound N from compound K. Predict the chemical reaction that occurs when compound L reacts with 2,4-…
Under certain conditions, mixing furan with maleic anhydride in diethyl ether yields a crystalline solid with a melting point of 114°C. When melting of this compound takes place; however, one can notice that the melt evolves a gas. If the melt is allowed to solidify, one finds that it no longer melts at 114°C but instead melts at 56°C. Provide an explanation for what is taking place.
Some alcohols undergo rearrangement or other unwanted side reactions when they dehydrate in acid. Alcohols may be dehydrated under mildly basic conditions using phosphorus oxychloride (POCl3) in pyridine. The alcohol reacts with phosphorus oxychloride much like it reacts with tosyl chloride, displacing a chloride ion from phosphorus to give an alkyl dichlorophosphate ester. The dichlorophosphate group is an outstanding leaving group. Pyridine reacts as a base with the dichlorophosphate ester to give an E2 elimination. Propose a mechanism for the dehydration of cyclohexanol by POCl3 in pyridine.

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