![Why Benzaldehyde and acetone can't do self-condensation in claisen-Schmidt reaction condensation? 2)In the second step of the same reaction, why do we add ethanol to form dibenzalideneacetone? | Homework.Study.com Why Benzaldehyde and acetone can't do self-condensation in claisen-Schmidt reaction condensation? 2)In the second step of the same reaction, why do we add ethanol to form dibenzalideneacetone? | Homework.Study.com](https://homework.study.com/cimages/multimages/16/q58f18182667827322217539.jpg)
Why Benzaldehyde and acetone can't do self-condensation in claisen-Schmidt reaction condensation? 2)In the second step of the same reaction, why do we add ethanol to form dibenzalideneacetone? | Homework.Study.com
![SOLVED: (12 points) The following Claisen-Schmidt condensation reaction forms an G,f-unsaturated e compound product; Icarbonyl H;c CH3 NaQH(aq) heat A) Give the structure Of this a,p-unsaturated carbonyl product: The ,B-unsaturated carbonyl product SOLVED: (12 points) The following Claisen-Schmidt condensation reaction forms an G,f-unsaturated e compound product; Icarbonyl H;c CH3 NaQH(aq) heat A) Give the structure Of this a,p-unsaturated carbonyl product: The ,B-unsaturated carbonyl product](https://cdn.numerade.com/ask_images/cfc35f36301e4a53a285211d63428f81.jpg)
SOLVED: (12 points) The following Claisen-Schmidt condensation reaction forms an G,f-unsaturated e compound product; Icarbonyl H;c CH3 NaQH(aq) heat A) Give the structure Of this a,p-unsaturated carbonyl product: The ,B-unsaturated carbonyl product
![An efficient and selective microwave-assisted Claisen-Schmidt reaction for the synthesis of functionalized benzalacetones | SpringerPlus | Full Text An efficient and selective microwave-assisted Claisen-Schmidt reaction for the synthesis of functionalized benzalacetones | SpringerPlus | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs40064-015-0985-8/MediaObjects/40064_2015_985_Figa_HTML.gif)
An efficient and selective microwave-assisted Claisen-Schmidt reaction for the synthesis of functionalized benzalacetones | SpringerPlus | Full Text
![Why Benzaldehyde and acetone can't do self-condensation in claisen-Schmidt reaction condensation? 2)In the second step of the same reaction, why do we add ethanol to form dibenzalideneacetone? | Homework.Study.com Why Benzaldehyde and acetone can't do self-condensation in claisen-Schmidt reaction condensation? 2)In the second step of the same reaction, why do we add ethanol to form dibenzalideneacetone? | Homework.Study.com](https://homework.study.com/cimages/multimages/16/q58f27891113962118695207.jpg)