![Write a reaction that would take place during the synthesis of dibenzalacetone if the concentration of acetone in the reaction mixture is not carefully controlled. | Homework.Study.com Write a reaction that would take place during the synthesis of dibenzalacetone if the concentration of acetone in the reaction mixture is not carefully controlled. | Homework.Study.com](https://homework.study.com/cimages/multimages/16/benzal____________acetone2814810025323216590.jpg)
Write a reaction that would take place during the synthesis of dibenzalacetone if the concentration of acetone in the reaction mixture is not carefully controlled. | Homework.Study.com
![SOLVED: NaOH OH NaOH benzaldehyde acetone benzaldehyde aldal additipn product NaOH OH NaoH Second aldol condensation product Second aldol addition product SOLVED: NaOH OH NaOH benzaldehyde acetone benzaldehyde aldal additipn product NaOH OH NaoH Second aldol condensation product Second aldol addition product](https://cdn.numerade.com/ask_images/be53a89347c8402f95ca12356d44a354.jpg)
SOLVED: NaOH OH NaOH benzaldehyde acetone benzaldehyde aldal additipn product NaOH OH NaoH Second aldol condensation product Second aldol addition product
![Write a reaction that would take place during the synthesis of dibenzalacetone if the concentration of acetone in the reaction mixture is not carefully controlled. | Homework.Study.com Write a reaction that would take place during the synthesis of dibenzalacetone if the concentration of acetone in the reaction mixture is not carefully controlled. | Homework.Study.com](https://homework.study.com/cimages/multimages/16/bezal_mechanism1565299619702549132.jpg)
Write a reaction that would take place during the synthesis of dibenzalacetone if the concentration of acetone in the reaction mixture is not carefully controlled. | Homework.Study.com
![The product formed by aldol condensation between benzaldehyde and acetone is benzalacetone. Its structure is: The product formed by aldol condensation between benzaldehyde and acetone is benzalacetone. Its structure is:](https://haygot.s3.amazonaws.com/questions/2040676_587744_ans_6bfcf05adb50447fb9d0a3c2ceefd0d6.png)
The product formed by aldol condensation between benzaldehyde and acetone is benzalacetone. Its structure is:
![Synthesis of jet fuel range high-density dicycloalkanes with methyl benzaldehyde and acetone - Sustainable Energy & Fuels (RSC Publishing) DOI:10.1039/D0SE01110J Synthesis of jet fuel range high-density dicycloalkanes with methyl benzaldehyde and acetone - Sustainable Energy & Fuels (RSC Publishing) DOI:10.1039/D0SE01110J](https://pubs.rsc.org/image/article/2020/SE/d0se01110j/d0se01110j-s2_hi-res.gif)
Synthesis of jet fuel range high-density dicycloalkanes with methyl benzaldehyde and acetone - Sustainable Energy & Fuels (RSC Publishing) DOI:10.1039/D0SE01110J
Scheme 1 Mannich reaction between benzaldehyde 1, aniline 2 and acetone 3. | Download Scientific Diagram
![The condensation reaction between one equivalent of acetone and two equivalents of benzaldehyde in presence of dilute alkali leads to the formation of: The condensation reaction between one equivalent of acetone and two equivalents of benzaldehyde in presence of dilute alkali leads to the formation of:](https://d1hj4to4g9ba46.cloudfront.net/questions/1491073_1698616_ans_9adb6edc4afd4dedbd3852cfb6a055e2.png)
The condensation reaction between one equivalent of acetone and two equivalents of benzaldehyde in presence of dilute alkali leads to the formation of:
![Highly tunable selectivity to benzaldehyde over Pd/ZrO2 catalysts in Oppenauer oxidation of benzyl alcohol using acetone as H-acceptor - ScienceDirect Highly tunable selectivity to benzaldehyde over Pd/ZrO2 catalysts in Oppenauer oxidation of benzyl alcohol using acetone as H-acceptor - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0926860X21000363-sc2.jpg)
Highly tunable selectivity to benzaldehyde over Pd/ZrO2 catalysts in Oppenauer oxidation of benzyl alcohol using acetone as H-acceptor - ScienceDirect
![Synthesis of 4-Hydroxy-4-(4-nitrophenyl)butan-2-one using p-Nitro Benzaldehyde and Acetone in Aqueous Micellar Media using L-Proline | Semantic Scholar Synthesis of 4-Hydroxy-4-(4-nitrophenyl)butan-2-one using p-Nitro Benzaldehyde and Acetone in Aqueous Micellar Media using L-Proline | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/fb3525c5cdbe6f070e4892f4cb2b282dcdced579/2-Figure1-1.png)