Chapter 19: Q19-10P (page 624)
Show the products you would obtain by acid-catalyzed reaction of cyclohexanonewith ethylamine, CH3CH2NH2, and with diethylamine, (CH3CH2)2NH.
Short Answer

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Chapter 19: Q19-10P (page 624)
Show the products you would obtain by acid-catalyzed reaction of cyclohexanonewith ethylamine, CH3CH2NH2, and with diethylamine, (CH3CH2)2NH.

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Compound A, , has an intense IR absorption at 1750 and gives the 13C NMR spectrum shown. Propose a structure for A.

The Meerwein–Ponndorf–Verley reaction involves the reduction of a ketone by treatment with an excess of aluminum triisopropoxide,.The mechanism of the process is closely related to the Cannizzaro reaction in that a hydride ion acts as a leaving group. Propose a mechanism.

Propose structures for ketones or aldehydes that have the following 1H
NMR spectra:
(a)
IR: 1715

(b)
IR: 1710

Draw structures of compounds that fit the following descriptions:
Draw structures corresponding to the following names:
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