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Lewis acid catalyst system for Claisen-Schmidt reaction under solvent free condition - ScienceDirect
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Nanoporous AlSBA-15 catalysed Claisen–Schmidt condensation for the synthesis of novel and biologically active chalcones | SpringerLink
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Claisen‐Schmidt Condensation using Green Catalytic Processes: A Critical Review - Yadav - 2020 - ChemistrySelect - Wiley Online Library
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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
![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)