Aldol Condensation For the following carbonyl compound, draw all possible enolates. Which is most stable? How do you know? Draw the mechanism for the condensation of this compound with itself, using an appropriate base.
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- What starting material is needed to synthesize the following reaction? Aldol condensation ?? HDraw all the main products to the reactions. No mechanism needed. Thank you!Aldol condensation is a reversible reaction and in fact aldols can be transform into the starting carbonyl compounds. Complete using arrows, the following retroaldol reaction
- Draw the reactions for the following products (any or all) (include all products).The mechanism for this reaction is the reverse of the one in Eg. 18-13. H;CO OCH3 H20 (excess) + 2 CH3OH An acetal (18-14) 1. Because acetal formation takes place under equilibrium conditions, the reaction shifted via Le principle. 10 Draw the complete, detailed mechanism for the reaction above.Major product and mechanism for this? Thank you!
- In the mechanism for acetal hydrolysis shown, the ring oxygen atom was protonated first, the ring was cleaved, and then the methoxy group was lost. The mechanism could also be written to show the methoxy oxygen protonating and cleaving first, followed by ring cleavage. Draw this alternative mechanism.Please draw the major products and explain the mechanisms thank youDraw the major organic product of the reaction conditions shown.
- a) The reaction below concerns an intramolecular Aldol condensation reaction. NaOH E CH3 H i) Redraw the above dicarbonyl compound and identify the most acidic hydrogen. ii) Draw the structure of two resonance contributors of the enolate anions derived from the above compound. iii) Propose the step-wise mechanism for the formation of the Aldol product and consequently the dehydrated product by showing all curve arrows.Draw the complete mechanism for this reaction. H₂SO4Draw a mechanism for the following reaction. Thank you!