![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
![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)
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
![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
![a) What is the step-wise mechanism for the Claisen-Schmidt reaction of acetone, with two equivalents of benzaldehyde? b) What is the product that results if only one equivalent of benzaldehyde is added a) What is the step-wise mechanism for the Claisen-Schmidt reaction of acetone, with two equivalents of benzaldehyde? b) What is the product that results if only one equivalent of benzaldehyde is added](https://homework.study.com/cimages/multimages/16/untitledm24382734759746660.png)
a) What is the step-wise mechanism for the Claisen-Schmidt reaction of acetone, with two equivalents of benzaldehyde? b) What is the product that results if only one equivalent of benzaldehyde is added
![Nanoporous AlSBA-15 catalysed Claisen–Schmidt condensation for the synthesis of novel and biologically active chalcones | SpringerLink Nanoporous AlSBA-15 catalysed Claisen–Schmidt condensation for the synthesis of novel and biologically active chalcones | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10934-019-00854-3/MediaObjects/10934_2019_854_Sch2_HTML.png)
Nanoporous AlSBA-15 catalysed Claisen–Schmidt condensation for the synthesis of novel and biologically active chalcones | SpringerLink
![Lewis acid catalyst system for Claisen-Schmidt reaction under solvent free condition - ScienceDirect Lewis acid catalyst system for Claisen-Schmidt reaction under solvent free condition - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403920306353-ga1.jpg)