Chapter 19: Q44E (page 648)
Paraldehyde, a sedative, and hypnotic agent, is prepared by treatment of acetaldehyde with an acidic catalyst. Propose a mechanism for the reaction.

Short Answer


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Chapter 19: Q44E (page 648)
Paraldehyde, a sedative, and hypnotic agent, is prepared by treatment of acetaldehyde with an acidic catalyst. Propose a mechanism for the reaction.



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Each of the following substances can be prepared by a nucleophilic
addition reaction between an aldehyde or ketone and a nucleophile.
Identify the reactants from which each was prepared. If the substance is an acetal, identify the carbonyl compound and the alcohol; if it is animine, identify the carbonyl compound and the amine; and so forth.

The SN2 reaction of (dibromomethyl)benzene, C6H5CHBr2, withNaOH yields benzaldehyde rather than (dihydroxymethyl)benzene,C6H5CH(OH)2. Explain.
Acid-catalyzed dehydration of 3-hydroxy-3-phenylcyclohexanone leads to an unsaturated ketone. What possible structures are there for the product? At what position in the IR spectrum would you expect each to absorb? If the actual product has an absorption at , what is its structure?
The 1HNMR spectrum shown is that of a compound with the formula C9H10O. How many double bonds and/or rings does this compound contain? If the unknown compound has an IR absorption at 1690 cm-1. , what is a likely structure?

Trans alkenes are converted into their cis isomers and vice versa on epoxidation followed by treatment of the epoxide with triphenylphosphine.Propose a mechanism for the reaction.
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