Chapter 21: Q36P-c (page 1129)
Show how you would accomplish the following synthetic transformations. You may use any necessary reagents.
Short Answer
Synthetic transformation for pyrrolidine to N-acetylpyrrolidine is show as,

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Chapter 21: Q36P-c (page 1129)
Show how you would accomplish the following synthetic transformations. You may use any necessary reagents.
Synthetic transformation for pyrrolidine to N-acetylpyrrolidine is show as,

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Which of the following proposed reactions would take place quickly under mild conditions?

An unknown compound of the molecular formula C5H9NO gives the IR and NMR spectra shown here. The broad NMR peak at d 7.55 disappears when the sample is shaken with D2O . Propose a structure, and show how it is consistent with the absorptions in the spectra.


For each set of IR and NMR spectra, determine the structure of the unknown compound. Explain how your proposed structure fits the spectra.
(a) C3H5NO


(b) C5H8O2

Show how you would synthesize each compound, starting with an ester containing no more than eight carbon atoms. Any other necessary reagents may be used.
d.Ph2CHOH
Two widely used pain relievers are aspirin and acetaminophen. Show how you would synthesize these drugs from phenol.

Aspirin Acetaminophen
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