Draw the major organic product expected from the crossed aldol condensation at elevated temperature. Draw only one product. H NaOH EtOH Δ Select Draw Rings More C H Erase
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- Draw all potential aldol renction produets. you exuude stereachmisty and may that no condensaton reuction asSume occur NaocHzcH3 t aldol reaution16. Draw the structure of the aldol self-condensation (followed by dehydration) product for each of the following compounds. If a compound does not undergo aldol self-condensation, explain why it does not. a) || CH3CHCH₂CH T CH₂ b)In micxed aldol condensation of acetone with excess benzaldehyde in the presence of NaOH what happens in initial step? oh attacks the carbonyl of acetate oh attacks the carbonyl carbon of benzaldehyde oh abstracts a proton from benzaldehyde oh abstracts a proton from acetone
- ← Draw the major product of the aldol condensation reaction between two of equivalents of this aldehyde with the conditions provided. Ignore inorganic byproducts. Prol H 1. H3O+, heat 2. Neutralizing work-up Drawing O At a CAldol condensation is a reversible reaction and in fact aldols can be transform into the starting carbonyl compounds. Complete using arrows, the following retroaldol reactionIf you react acetaldehyde and acetone in the precensce of NaOH in H2O, how many aldol condensation products will form. I need help with drawing a detailed mechanism.
- What starting materials are needed to synthesize each compound using an aldol or similar reaction?Draw the structure of the major aldol product (prior to possible dehydration) of the following reaction without specifying stereochemistry. 0 dilute aqueous NaOH 0-5° • You do not have to consider stereochemistry. • If no reaction occurs, draw the organic starting material. ChemDoodle 3bArSO,H Draw curved arrows to show the movement of electrons in the following step of an acid-catalyzed aldol condensation reaction. Arrow-pushing Instructions Hjö: H-Ö- -Ar H. Ar O=h=0
- Draw the complete reaction mechanism for the crossed aldol condensation between benzaldehyde and the given aldehyde below, utilizing NaOH as the base and water as reagent. H or" OExplain mechanism for Retro aldol reaction ?Draw the enolate anion and the carbonyl that would be needed to make this product through an aldol condensation reaction. O oo Draw Enolate Anion Q