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- From each pair, select the stronger base. Then draw the conjugate acid of the strong base below. CH3CH20 or CH3CEC • You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • You do not have to include lone pairs in your answer. C opy aste4) what is pur pose of using 2n dust in CH,COOH for a cetylation reaction?Draw mechanism for fischer esterification using the reagents benzoic acid, methanol and sulfuric acid using the general mechanism attached as reference. HINT: You just need to replace the Rs in the general mechanism for the actual groups in your reagents.
- 1) Propose a mechanism that explains the formation of the given byproduct from the starting materials. Use curved arrows to show movement of electrons, show all intermediates. Label Nu:, E*, acid, and base where appropriate. Hx(O₂Al/Si)y HOCH2CH3Please don't provide handwritten solution.....CULT MAN Malonic ester synthesis Write the reaction showing all intermediates when H₂C(CO₂Et)2 (diethyl malonate) is reacted followed by 1) ethyl iodide; 2) NaOH; 3) H3O*; 4) A. Hint: Remember that ß-oxo carboxylic undergo decarboxylation (loss of 1 equivalent of CO₂) when strongly heated. ofarbaye a el alzartiny A-291clone bns alon3- SOE with NaOEt acids
- Write the product of the following reaction. Indicate the mechanism of the reaction involved.(b) Ph. Ph H Ph, Ph-P: Ph H ? Modify the given copy of the starting aldehyde to draw the major product. Be sure to include stereochemistry in your drawing.Draw the organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. HCI 0:0 Q
