![When acetone reacts with dilute aqueous solution of Ba OH 2, the product obtained is calledA. diacetone alcoholB. PhoroneC. crotonaldehydeD. Acetophenone When acetone reacts with dilute aqueous solution of Ba OH 2, the product obtained is calledA. diacetone alcoholB. PhoroneC. crotonaldehydeD. Acetophenone](https://search-static.byjusweb.com/question-images/byjus/infinitestudent-images/ckeditor_assets/pictures/269514/content_aldol-acetone.png)
When acetone reacts with dilute aqueous solution of Ba OH 2, the product obtained is calledA. diacetone alcoholB. PhoroneC. crotonaldehydeD. Acetophenone
![Catalysts | Free Full-Text | Aldol Condensation of Furfural with Acetone Over Mg/Al Mixed Oxides. Influence of Water and Synthesis Method Catalysts | Free Full-Text | Aldol Condensation of Furfural with Acetone Over Mg/Al Mixed Oxides. Influence of Water and Synthesis Method](https://www.mdpi.com/catalysts/catalysts-09-00203/article_deploy/html/images/catalysts-09-00203-g001-550.jpg)
Catalysts | Free Full-Text | Aldol Condensation of Furfural with Acetone Over Mg/Al Mixed Oxides. Influence of Water and Synthesis Method
![Competitive Adsorption of Methanol–Acetone on Surface Functionalization (−COOH, −OH, −NH2, and −SO3H): Grand Canonical Monte Carlo and Density Functional Theory Simulations | ACS Applied Materials & Interfaces Competitive Adsorption of Methanol–Acetone on Surface Functionalization (−COOH, −OH, −NH2, and −SO3H): Grand Canonical Monte Carlo and Density Functional Theory Simulations | ACS Applied Materials & Interfaces](https://pubs.acs.org/cms/10.1021/acsami.9b10804/asset/images/large/am9b10804_0012.jpeg)
Competitive Adsorption of Methanol–Acetone on Surface Functionalization (−COOH, −OH, −NH2, and −SO3H): Grand Canonical Monte Carlo and Density Functional Theory Simulations | ACS Applied Materials & Interfaces
![Potential energy profiles for the OH + acetone reaction system using... | Download Scientific Diagram Potential energy profiles for the OH + acetone reaction system using... | Download Scientific Diagram](https://www.researchgate.net/publication/230794686/figure/fig2/AS:300360783679490@1448622999454/Potential-energy-profiles-for-the-OH-acetone-reaction-system-using-the-calculated.png)
Potential energy profiles for the OH + acetone reaction system using... | Download Scientific Diagram
![Reaction of Hydroxyl Radical with Acetone. 2. Products and Reaction Mechanism | The Journal of Physical Chemistry A Reaction of Hydroxyl Radical with Acetone. 2. Products and Reaction Mechanism | The Journal of Physical Chemistry A](https://pubs.acs.org/cms/10.1021/jp0273023/asset/images/medium/jp0273023f00010.gif)
Reaction of Hydroxyl Radical with Acetone. 2. Products and Reaction Mechanism | The Journal of Physical Chemistry A
![SOLVED: Provide the mechanism for acid catalyzed enolization of acetone in aqueous solution. H3O OH What product is formed when the following di-ketone undergoes the intramolecular Aldol condensation reaction? Provide the reaction SOLVED: Provide the mechanism for acid catalyzed enolization of acetone in aqueous solution. H3O OH What product is formed when the following di-ketone undergoes the intramolecular Aldol condensation reaction? Provide the reaction](https://cdn.numerade.com/ask_images/260992ef35064c469c0ed54a4884f73f.jpg)
SOLVED: Provide the mechanism for acid catalyzed enolization of acetone in aqueous solution. H3O OH What product is formed when the following di-ketone undergoes the intramolecular Aldol condensation reaction? Provide the reaction
![Upgrading bio-based acetone to diacetone alcohol by aldol reaction using Amberlyst A26-OH as catalyst | SpringerLink Upgrading bio-based acetone to diacetone alcohol by aldol reaction using Amberlyst A26-OH as catalyst | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs11144-022-02168-z/MediaObjects/11144_2022_2168_Fig2_HTML.png)
Upgrading bio-based acetone to diacetone alcohol by aldol reaction using Amberlyst A26-OH as catalyst | SpringerLink
![Devise a synthesis of the below compound using acetone (CH3)2C=O is the only source of carbon atoms. You may use any needed organic or inorganic reagents. | Homework.Study.com Devise a synthesis of the below compound using acetone (CH3)2C=O is the only source of carbon atoms. You may use any needed organic or inorganic reagents. | Homework.Study.com](https://homework.study.com/cimages/multimages/16/untitledlk809971296614686806.png)
Devise a synthesis of the below compound using acetone (CH3)2C=O is the only source of carbon atoms. You may use any needed organic or inorganic reagents. | Homework.Study.com
![The product formed when acetone is heat with `Ba(OH)_(2)` is : - Sarthaks eConnect | Largest Online Education Community The product formed when acetone is heat with `Ba(OH)_(2)` is : - Sarthaks eConnect | Largest Online Education Community](https://learnqa.s3.ap-south-1.amazonaws.com/images/16119406431526449133ZCeGCIcRPjug9tff.png)
The product formed when acetone is heat with `Ba(OH)_(2)` is : - Sarthaks eConnect | Largest Online Education Community
![Acetone. Molecular model of the ketone acetone (C3.H6.O). This colourless flammable liquid, widely used as a solvent, is the simplest example of a ketone. It is also known as propanone. Atoms are Acetone. Molecular model of the ketone acetone (C3.H6.O). This colourless flammable liquid, widely used as a solvent, is the simplest example of a ketone. It is also known as propanone. Atoms are](https://c8.alamy.com/comp/HACNWC/acetone-molecular-model-of-the-ketone-acetone-c3h6o-this-colourless-HACNWC.jpg)