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The result of performing an aldol condensation leads into the formation of unsaturated
ketone products since ketones are less reactive than aldehydes in aldol condensation because the
carbonyl of the ketones are histerically hindered and is electronically not as susceptible to
nucleophilic attack. Another reason would be because the aldehyde used, dont have -
hydrogens, so they cannot react with themselves; one such example is the experiment performed.
Also, dehydration is more favorable because the product has extended conjugations and
precipitates out of the solution. The aldehyde derivative used was trans-cinnamaldehyde and the
ketone derivative was cyclopentanone. Since the ketone derivative used was cyclopentanone and
is a symmetrical ketone, it will undergo double aldol condensation since it will be able to react
with two molecules of another carbonyl compound under basic conditions. Since the product is
highly conjugated, the hydration will be facile. The reaction of cyclopentanone and trans-
cinnamaldehyde (1:2) leads into the formation of the aldol product, (2E,5E)-2,5-Bis[(2E)-3-
phenyl-2-propen-1-ylidene]cyclopentanone. The aldol product is yellow-colored due to the
narrow HOMO-LUMO gap because of the extensive conjugation which is the reason why the
which corresponds
to the phenyl group (