a) Draw mechanism/product for aldol reaction: NaOet ethanol (solvent) c) Final product if result is protonated...
Draw a mechanism for a green aldol synthesis without solvent. using 3,4-dimethoxybenzaldehyde, 1-indanone, NaOH, HCl, ethanol and water
10.(7pts) Draw the mechanism for the following self Aldol Condensation. NaOH,H,O, heat Bonus: 5 pts no partial credit. All correct or nothing. Predict the product and draw a mechanism for the following transformation. Sune NaOET EtOH(solvent)
Draw a full mechanism for the Aldol condensation reaction and predict the product. Show all the elementary step(s) being sure to include arrows, important electron pairs and any formal charges if needed. SHORT ANSWER # 28: Draw a full mechanism for the following transformation Aldol condensation reaction and predict the product. Show all the elementary step(s) being sure to include all arrows, important electron pairs and any formal charges if needed. (8 points) NaOH, HAO heat Aldol condensation product H
while the In the aldol condensation reaction, the enolate anion is a(n). ethanol serves as a(n) O electrophile, nucleophile nucleophile, acid O electrophile solvent nucleophile, solvent Question 28 (3 points) Identify the energetically favored product of the following reaction: H3PO4 d Heat OH CU
Give the major organic product of each reaction. 8. a. LDA н b. H c. mild H NaOH, H,O н a, LDA b. f. н NaOH, H,O, heat c. mild H NaOH, H,O O NaOH, H,O H CYD a. LDA b. d. h. NaOH, H,O, heat c. mild H*, heat 9. Give the major organic product of each intramolecular Aldol reaction. NaOH, H,O a. heat H NaOH, H2O b. heat NaOH, H,O NaOH, H20 d. heat 10. Propose starting materials...
10. Propose starting materials needed to synthesize each molecule through an aldol reaction. a. b. c. d. H f. 11. Give the curved arrow mechanism for each Claisen reaction. a. NaOEt a. b. mild H EtO EtO 1 11 continued a. NaOMe MeO b. b. mild H МеO a. NaOEt с. b. mild H
Draw the organic product for this reaction. NaOET Draw the organic product for this reaction. C-S
14. Reaction of the following diester with NaOEt followed by mild Ht makes product G, not product H. Explain why there is a preference for forming product Gover H. a. NaOEt OEt not "OEib mild H* 15. Give the curved arrow mechanism for the decarboxylation and keto-enol tautomerism steps in this reaction (from 3 to K). مه-حل-ا مل a. NaOEt b. H, H30, heat
Question 1 Match each reagent with its role in aldol condensation reaction. Not yet answered D-anisaldehyde Choose... Points out of 10.00 dium hydroxide Choose... P Flag question acetophenone Choose... ethanol Choose... Question 2 Not yet answered To purify the aldol condensation product you will have to recrystallize it from methanol. Give the steps in recrystallization procedure the appropriate order numbering. Points out of 10.00 The compound is kept under vacuum for 10 min Choose... + P Flag question The solution...
SHORT ANSWER#28: Draw a full mechanism for the following transformation Aldol condensation reaction and predict the product. Show all the elementary step(s) being sure to include all arrows, important electron pairs and any formal charges if needed. (8 points) NaOH, HO heat Aldol condensation product H Academic Honesty Statement: I have completed my drawing and shown the computer my answer. I understand that any alteration to the answer that was shown to the camera before uploading to GradeScope will result...