This is a Solvent-Free Synthesis of Chalcones: Claisen-Schmidt Condensation The Chalcone starting materials are: p-bromoscetophenone (solid)...
This is a Solvent-Free Synthesis of Chalcones: Claisen-Schmidt Condensation The Chalcone starting materials are: p-bromoscetophenone (solid) p-chlorobenzaldehyde (solid) 11. [3 points) Draw the curved-arrow mechanism for your chalcone from the starting materials that you used. Explain why this reaction produces only one chalcone and not a mixture.
8. 11 pt 4-chlorobenzaldehyde and 4-bromoacetophenone are both solid starting materials for the synthesis of substituted chalcone. When both of these compounds are ground with solid sodium hydroxide, the entire reaction mixture turns liquid. Explain why the solid reactants turn liquid when intimately mixing them. (Hint: What are the final products of the reaction?)
8. 1 pt] 4-chlorobenzaldehyde and 4-bromoacetophenone are both solid starting materials for the synthesis of substituted chalcone. When both of these compounds are ground with solid sodium hydroxide, the entire reaction mixture turns liquid. Explain why the solid reactants turn liquid when intimately mixing them. (Hint: What are the final products of the reaction?)
Need help, numbers 3-6 please show work. and fill out table of chemicals for all chemical used. calculate mmol in the table as well show work please and each of these must be listed in its own row. There are 10 column headings: IUPAC name OR common name, structure, CAS number (Chemical Abstract Service number) molecular mass, melting point (if applicable), boiling point (if applicable), solubility (in water, if applicable), density, amounts to be used in the experiment, and the...