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- 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 PhWhat aldol product is formed when two molecules of butanal react together in the presence of base? What reagents are needed to convert this product to each of the attached compounds?What aldol product is formed when two molecules of butanal react together in the presence of base? What reagents are needed to convert this product to each of the attached compound?
- How can I synthesize this? with SuccinaldehydeWhat aldol product is formed when two molecules of butanal react together in the presence of base? What reagents are needed to convert this product to each of the following compounds?Is the reaction possible? are there any ways to synthesize the aldol product without having other products? Does using LDA will arrive to a single aldol product?
- What conjugate base must be formed during the E1cb mechansim in an aldol condensation reaction running under basic conditions? А. enol В. B-hydroxy carbonyl C. a,B-unsaturated carbonyl D. enolatePlease provide the major product of the following reaction via an E2 mechanism. ... Br KO Bu (one equivalent) t-BuOH4. Propose how to make the following alkene through a Wittig reaction and draw the mechanism. où