Show the mechanism for a base-catalyzed aldol condensation of the reaction. Use any appropriate base. Show...
1. Draw the complete curved-arrow mechanism for the base-catalyzed aldol condensation to form dehydrorheosmin (or dehydrozingerone) from acetone and 4-hydroxybenzaldehyde (or vanillin). (2 points)
2. Draw and name the compound resulting from the aldol condensation of vanillin with creatinine. CHE Vanillin Creatinine
aldol condensation reaction Question 3: Is this reaction acid or base catalyzed? Tell the name of the base used. Question 4: What is the role of ethanol in the experiment? Question 5: Why 1.0 M HCl is used at the end of the experiment? Question 6: 4-nirobenzaldehye cannot undergo aldol condensation reaction by itself in the presence of strong base, give the reason for that?
Define (reaction only) the base catalyzed cross-aldol condensation reaction between excess benzaldehyde and propanaldehyde (No mechanism needed)!
Base-catalyzed crossed aldol condensation followed by the oxa-michael addition reaction mechanism for the reaction above! Thank you!! 20 10 F4 FOF2 DOO FS F9 0 A 6 7 8L 0 diiso propylamine (DIPA) EtoH + HP
Product is 5-(4-hydroxy-3-methoxybenzal)creatinine. Will rate ASAP. Thank you!! Questions: 1. Give the step-to-step mechanism for the condensation of vanillin and creatinine. (based on what you did for this experiment, decide if you have an acid or base catalyzed reaction) 2. This aldol condensation does not require a base. Why? 3. What is the major difference between the IR spectra of vanillin and the condensation product?
Predict major product (WITH MECHANISM) of the base-catalyzed aldol condensation with dehydration of: methyl phenyl ketone + 2,2-dimethylpropanal
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
11. What would be the major organic product of this base-catalyzed reaction? 8. What would be the major product of this reaction? CH CH2CH CH (CH)yC-CH+CH.CCH, O o (A) CH-CH.CH,сснсн сH,CH, (в) сн.CH.CH,CH, он снсH,CH,COO, он о CH CH CH,CHCHCH сHCH, CH CH9 снс-CH-с—сн сн, (A) (C) OH O CHy сне-с-с-сн, сH, сн, (B) он (D) CH смссн,-с-с-сн, CH он сн снссн сн-с-сн, сн, (C) CHCH CH CHCH,CH CH,CH 9. Which of these is not a step in the mechanism...
a) Draw all of the products obtained from the base-catalyzed aldol condensation reaction between butanal and pentanal(crossed and self) b) Show the half reaction corresponding to the reduction of permanganate ion to manganese dioxide. Show the half reaction corresponding to the oxidation of cyclopentene to 1,2 dihydroxycyclopentane. Add the two half-reactions together to give the overall net ionic equation of the oxidation of cyclopentene to 1,2 dihydroxycyclopentane using permanganate ion. Can anyone help me out?