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- Draw the structure of the hydroxyaldehyde product from the self-aldol reaction of each of the following aldehydes: (a) propanal; (b) phenylethanal; (c) 3-phenylpropanal; (d) benzaldehyde.Q3: write the structure and the mechanism of the aldol condensation product of each of the aldehydes. Also one of these aldehydes can undergo aldol addition, but not able condensation. Which one? Why:- a) H₂C CH₂ 3-methylbutanal b) سابع مرکب امرول H₂C 2-methylbutanalComplete the following syntheses by filling in the missing structures or reagents! Thank you!
- Identify the electrophile and the nucleophile in each of the following reaction steps and then draw curved arrows to illustrate the bond-making and bondbreaking processes.1. Provide the mechanism of the reaction shown in the picture. 2. Explain why it cannot be done in basic conditions. 3. Why is the enol tautomer favored over the keto tautomer? Ph H3C OH H H3O+/H₂O HO H3C PhPlease give the missing information like structure of reagents, products, etc..
- ochem help with reagents... in the following syntheses please provide the reagents needed to complete each.provide the mechanism given the product and starting material along with any reagents neededList the appropriate reagents that can be used in places with questions in the following series of reactions
- List the appropriate reagents that can be used in places with question marks in the following series of reactions.What is the major product of the following ozonolysis reaction? and and HOComplete the following reaction diagram by giving either the reaction conditions or the missing products. The reaction mechanisms are not required.