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- how do i go about this mechanism? is it a cross aldol reaction?Modify the given starting materials to give their self aldol products.T 3. The first product made in an acid catalyzed hydration reaction of an alkyne is an unstable functional group called an enol. Enols quickly tautomerize to a carbonyl (either ketone or aldehyde). Starting with the enol, sulfuric acid, and water, draw the complete, detailed mechanism for this acidic tautomerization reaction below. Q Search 6 & 7 Alkyne HgSO4 H₂SO4 H₂O 8 fg OH Enol lyi 9 f10 Ketone O f12 +
- 4) When a mixture of two different compounds both containing a hydrogens are placed under acidic or basic conditions, crossed aldol products can be formed. By either self-condensation or cross condensations. Draw the 4 aldol and 4 a.B-unsaturated ketones that can be made from the following mixed system. -OH 4 products One way to control this is by either having only one compound with a hydrogens or by reacting the desired nucleophile with lithium diisopropylamide (LDA) before addition of second carbonyl. The issue here is that this reaction stops at the aldol unless excess base is used. он LDA OH heat Show a synthetic scheme of how to use the following carbonyls to control the formation of each cross product (i.e. each as nucleophile and electrophile, two reactions). andPlease give the reagents that will perform the following reaction.Hi! I am having a tough time trying to figure out the synthesis to this reaction. Can you help me?
- a) Show the reaction mechanism for the following multistep transformations. Show all reagents and the intermediate structures. Br OH from and b) Propose a correct retrosynthetic analysis of (E)-1,3-di(furan-2-yl)prop-2-en-1-one following an aldol condensation reaction.I need a detailed mechanism for the aldol condensation reaction bewtween cyclobutanone and p-chlorobenzaldehyde. Please help.Synthesize the product below. Please try to use Wittig at one or two time in this synthesis. Wittig reagents must be shown how to synthesize from an alkyl halide.
- Part 1 - Draw the full mechanism for the cross-aldol reaction between acetone and benzaldehyde Part 2 - Draw the product that would form if we added only one mole each of acetone and benzaldehyde. Part 3 - After forming the initial product, we see the elimination of water to give the final product as a solid that we collect. What drives this product formation?Could you help show the reagent and the synthetic intermediates to the product?1. Discuss the role of the Aldol condensation reaction in the synthesis below. What specific reaction was used in the synthesis? What is the importance of the aldol reaction in the entire synthetic approach? 2. Show the detailed reaction mechanism involved in their corresponding specific parts in this syntheses.