Chapter 21: Q36P-d (page 1129)
Show how you would accomplish the following synthetic transformations. You may use any necessary reagents.
Short Answer
Synthetic transformation for -aminobutyric acid to pyrrolidine is show as,
Chapter 21: Q36P-d (page 1129)
Show how you would accomplish the following synthetic transformations. You may use any necessary reagents.
Synthetic transformation for -aminobutyric acid to pyrrolidine is show as,
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Get started for freeOne mole of acetyl chloride is added to a liter of triethylamine, resulting in a vigorous exothermic reaction. Once the reaction mixture has cooled, 1 mole of ethanol is added. Another vigorous exothermic reaction results. The mixture is analyzed and found to contain triethylamine, ethyl acetate, and triethylammonium chloride. Propose mechanisms for the two exothermic reactions.
When ethyl 4-hydroxybutyrate is heated in the presence of a trace of a basic catalyst (sodium acetate), one of the products is a lactone. Propose a mechanism for the formation of this lactone.
Name the following carboxylic acid derivatives, giving both a common name and an IUPAC name where possible.
a.
b.
c.
d.
e.
f.
g.
h.
i.
j.
k.
l.
m.
n.
o.
p.
q.
r.
Show how you would synthesize each compound, starting with an ester containing nomore than eight carbon atoms. Any other necessary reagents may be used.
a. PH3C-OH
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.
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