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Q: What is the final product of the Claisen condensation of propanone and excess ethyl ethanoate.
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Show the product of Claisen condensation of ester.
Q.) Methyl hexanoate in the presence of sodium methoxide
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- Show the product formed as a result of the reaction between propanoic acid and benzylalcohol in an acidic environment by writing down the reaction mechanism.Perform a retrosynthetic analysis and suggest a synthesis of the target molecule (on the left) from the given starting material (on the right). (any reagents maybe usedShow the product formed as a result of the reaction between propanoic acid and benzyl alcohol in an acidic environment by writing down the reaction mechanism.
- Show a mechanism for the conversion of any aldehyde or ketone and any alcohol (as solvent) to the acetal with added gaseous HCL as the catalystShow the product formed as a result of the reaction between propanoic acid and benzylalcohol in an acidic environment by writing the reaction mechanism together.Show how the m-bromobenzoic acid can be synthesized from benzene:
- If the melting point obtained was 144 degrees Celsius, which structure corresponds to the mixed aldol product obtained.When alcohol A is heated with base as shown below, the expected epoxide does not form. Explain why this is the case, Using strcutures to support your answerPlease provide a detailed mechanism for the synthesis of dibenzalacetone and say what product would be made if only 1 equivalent of acetone was used!
- a) Put these three common types of carbonyl compound in order of decreasing reactivity ester amide acid chloride b) For the least reactive, show the interconversion to its other resonance form: How does this electron delocalisation make it stable? c) For the most reactive, draw the mechanism of its undergoing hydrolysis (reaction with H2O): Why makes this type of carbonyl so reactive to nucleophiles?Draw a detailed, arrow-pushing mechanism for the conversion of benzoic acid to methyl benzoate under acid conditions with methanol.draw the step-wise mechanism (arrow pushing) of the acid catalyzed fischer esterification for the formation of benzyl propanoate