Draw the major product of the Claisen condensation reaction between two molecules of this ester. Ignore inorganic byproducts. 1. NaOCH3/CH3OH 2. Acidic workup
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- Please complete the following reaction showing all arrow pushing mechanisms. What is the name of this reaction?Please propose a synthesis of the target molecule using as many steps or reagents and answer these questions. 1. Why use chemoselectivity as the functional group and not another? 2. Why regioselectivity? 3. Why stereoselectivity? 4. What are the changes in the oxidation state?During benzoic acid synthesis, the Girgnard reagent is formed when this atom ______ inserts itself causing the initial type of carbon ____ to be changed to this final type of carbon ____. Please help fill in the blanks above.
- In a few sentences, briefly explain the difference between acid catalyzed and base promoted enolation of aldehydes and ketones.Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. You do not have to consider stereochemistry. Draw the enolate nucleophile in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu.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 used
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