Please show mechanism of product a (vanillyl acetate) the base catalyzed product and product b (...
Please interpret and record spectral data for base and acid catalyzed products of vanillin esterfication. Base product name: Vanillyl acetate Acid product name: 4-acetyloxy-3-methoxyphenyl methanediyl diacetate HNMR acid CNMR acid HNMR base CNMR base CHOM 237 Esterification of Vanilla Acid Catalyzed Product 7.6 7.5 7.4 CHM 237 Esterification of Vanillin Acid Catalyzed Product 190 180 170 160 150 140 130 120 110 100 90 80 70 60 50 40 30 20 10 Oppm CM 237 Esterification of Vanillin Base Catalysed...
Show the mechanism for a base-catalyzed aldol condensation of the reaction. Use any appropriate base. Show the mechanism for an acid-catalyzed aldol concentration of the reaction. use any apporproate acid. 2. Draw and name the compound resulting from the aldol condensation of vanillin with creatinine. сн, NH но- 160°C NH CH Vanillin Creatinine 2. Draw and name the compound resulting from the aldol condensation of vanillin with creatinine. сн, но- NH 160 C NH сH, Vanillin Creatinine
NMR for [4-(acetyloxy)-3-methoxyphenyl]methanediyl diacetate. Is this correct? 17.40 7.26 7.17 7.04 -3.87 2.35 2.14 Acid-catalyzed vanillin esterification possible product 2 (esterification of alcohol and aldehyde substituent) Simulated High Resolution Spectrum –7.40 –7.26 212- A OOCH3 G F E CEⓇ Hec. AHHH 7.4 7.0 CH 7.3 7.2 7.1 Chemical Shift A,B 13.041 6.101 11.5 10.5 9.5 8.5 7.5 6.5 5.5 4.5 Chemical Shift 3.5 2.5 1.5 0.5 -0.5 -1.5
HW 22: Enolates 1. Provide a detailed, stepwise mechanism for the base-catalyzed enolization (keto enol tautomerism) of acetaldehyde. 2. Provide the major organic product of the folowing reaction. 3. Provide the major organic product of the following reaction LDA 4. Which of the following ketones will give a positive iodoform test? A) 4-heptanone D) cyclohexanone B) 3-hexanone C)2-hexanone 5. Provide the major organic product of the following reaction. 6. Provide the structure of the major organic product which results when...
What is the mechanism for base-catalyzed transesterification with methanol where the ester reacts with an alcohol solvent to form a new ester that contains the alcohol's OR group? Please draw out mechanism and explain. the reaction will use the reagents XS NaOCH3 (from NaOH, CH3OH) to convert vegatable oil (a fatty acid triester) to glycerol and 3 moles of methyl oleate (biodiesel)
Please show the mechanism with acid. 2. Write the complete reaction mechanism for the KCN-catalyzed reaction. Show all electron flow with arrows and show all intermediate structures он CH-COOH O но CN = C H20* Who. HHCEN NAOH HO cyanolydrin + NaCN + H2O
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?
show a mechanism of formatiin if the following enol under base catalyzed conditions We were unable to transcribe this imageShow a mechanism of formation of the following enol under base-catalyzed conditions: For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do n use abbreviations such as Me or Ph. Step 1 0 Get help answering Molecular Drawing question Draw step 1 of...
Please write the mechanism for the acid catalyzed hydrolysis of this compound. Show intermediates, formal charges, and lone pairs. Use curvy arrows. 0
please show correct mechanism of all three questions. Please do all three questions. oil) and follow the label 180 9. rropose a mechanism for the formation of isoamyl acetate (banana oul and through your mechanism, and show where it is found sm, and show where it is found in the products (13 points) HO он HO acetic acid 3-methylbutan-1-01 isoamyl acetate O 18 (3/18) IV. Mechanism (18 points) 7. Please show the mechanism for the thermal decarboxylation of the carboxylic...