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What side products are formed in the aldol condensation of dibenzalacetone?

Answer 1

Ruby Allen

Dibenzalacetone does not undergo the aldol condensation.

However, dibenzalacetone is formed by a crossed aldol condensation between benzaldehyde and acetone.

Some of the side products expected in this reaction could be:

1. Benzalacetone

From incomplete condensation of the benzaldehyde.

2. Diacetone alcohol (4-hydroxy-4-methylpentan-2-one) and mesityl oxide (4-methylpent-3-en-2-one)

From the aldol condensation of acetone with itself, followed by dehydration of the β-hydroxyketone.

#2"CH"_3"COCH"_3 → underbrace(("CH"_3)_2"C(OH)CH"_2"COCH"_3)_color(red)("diacetone alcohol") → underbrace(("CH"_3)_2"C=CHCOCH"_3)_color(red)("mesityl oxide") #

3. Benzyl alcohol and benzoic acid from the Cannizzaro reaction of benzaldehyde.

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Answer 2

Brooklyn Barber

The aldol condensation of dibenzalacetone can produce side products such as dehydration products, enones, and polymeric substances.

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.