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Step by step
Solved in 3 steps with 1 images
- how the CH2Br would affect the E1 reaction for this molecule?What is the structure of the product in step 4?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.
- Why is the reaction of the type shown below usually done? a.To make an aldehyde or ketone less water soluble b.To make the molecule more reactive c.To protect a ketone or aldehyde carbonyl d.To increase the oxygen content e.To make the alpha hydrogens more acidicWhat reagents would best install the aldehyde CHO functional group?What is the main organic product of the reaction in Figure 11?
- Draw the major organic product for the reaction in Part 1 and for the reaction in Part 2.Based on your answer to the above question and the structures you draw in question 1, what group/bond in the structure that causes the increased reactivity towards bromine addition?What are the important mechanisms that should be highlighted in this image? How do they work together to create the final product?
- Fill in the fields (reagent or products) left blank in the reaction below.a. Can you predict an undesirable side reaction that might occur using ethanol as a solvent that would not occur if we used THF as a solvent?b. Based on your knowledge of SN2 reactions, what would happen if we used 1-ethyl-2- naphthoxide instead of 2-naphthoxide? Explain.Write all the steps involved using the reagents given on the starting materials and draw the final product?