consider the aldol condensation between dibenzyl ketone and benzil in strong base. a reaction was performed in which 0.28 g of dibenzyl ketone was reacted with 0.28 g of benzil to make 0.34 g of 2,3,4,5‑tetraphenylpentadienone. calculate the theoretical yield and percent yield for this reaction.

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Johnny8962 Johnny8962

08-09-2022
Chemistry

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consider the aldol condensation between dibenzyl ketone and benzil in strong base. a reaction was performed in which 0.28 g of dibenzyl ketone was reacted with 0.28 g of benzil to make 0.34 g of 2,3,4,5‑tetraphenylpentadienone. calculate the theoretical yield and percent yield for this reaction.

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tripatsingh039 tripatsingh039 · Answer 1 · 2022-09-11T16:28:00+02:00

In organic chemistry, an aldol condensation is a condensation reaction in which an enol or enolate ion combines with a carbonyl chemical to produce a -hydroxyaldehyde or -hydroxyketone, which is then dehydrated to produce a conjugated enone.

Aldol condensations are significant in the synthesis of organic compounds because they offer a reliable method for forming carbon-carbon bonds. Aldol condensation, for instance, occurs during the Robinson annulation reaction sequence, and the Wieland-Miescher ketone product is a crucial building block in numerous chemical syntheses. Aldol condensations are frequently studied as a useful bond-forming reaction that exemplifies significant reaction mechanisms in university-level organic chemistry coursework. in the standard form.

Learn more about Aldol condensation here-

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