If you brominate the product from the nitration of methyl benzoate, what would the major product be? Write a complete reaction.
If you brominate the product from the nitration of methyl benzoate, what would the major product...
Write a mechanism for the nitration of methyl benzoate (major product only) Include formation of the electrophile from the reaction of nitric acid with sulfuric acid. Only one resonance structure is needed for the intermediate in the EAS portion of the mechanism
draw a mechanism for methyl 3 benzoate 2. For the nitration of methyl benzoate: Which product did you get? What evidence doyou have for this? Wasyourproduct pure? Whatevidence do you have for this? Explain your a. b. evidence. c. Draw the mechanism for the product you got. d. Calculate percent yield. Show your work
4. Calculate the theoretical yield of product in the nitration of methyl benzoate if the reaction was begun with 0.400 g of methyl benzoate. (Show ALL work please.)
What is the purpose of the following in the experiment for Nitration of Methyl Benzoate and what is the reaction scheme for the experiment 1. Sulfuric Acid 2. Methyl Benzoate 3. Nitric Acid 4.Ethanol
Post Lab Questions for Nitration of Acetanilide, Nitration of Methyl Benzoate, Nitration of Phenylacetonitrile, Nitration of Phenol. 1. What product(s) do you expect to be formed in the nitration of phenol? Why? 2. All three of the nitrophenols have boiling points well above 200°C. Explain clearly why it was possible to distill something with such a high boiling point when the temperature of the distillate never rose much above 100°C. 3. What product did you actually obtain in the distillate?...
What would be the product(s) of this reaction if toluene replaced methyl benzoate? If only concentrated nitric acid were used in this reaction, will that increase the % yield of the reaction? And why? What is the function of concentrated sulfuric acid? Please use a reaction equation to show your answer. These are questions from my organic chemistry lab regarding the nitration of methyl benzoate to form m-nitrobenzoate through electrophilic aromatic substitution rxn.
For the nitration of methyl benzoate: a. Which product did you get? What evidence do you have for this? b. Was your product pure? What evidence do you have for this? Explain your evidence. c. Draw the mechanism for the product you got. For the bromination of acetanilide: a. Which product did you get? What evidence do you have for this? b. Was your product pure? What evidence do you have for this? Explain your evidence. c. Draw the mechanism...
A minor product in the nitration of methyl benzoate is a dinitro product. Of the four structures below, which one of them is the most likely dinitro product? On a separate sheet, explain your choice.
This question is for the Nitration of Methyl Benzoate, the final product is Methyl 3 nitrobenzoate but I dont know how to get the byproduct produced during this reaction. Please use the expanded structural formulas and show a mechansim on how that occurs and on the right please provide a description of what is going on in that step/mechanism, ie an Sn1 or E1, etc. b. As stated in the Lab Manual for this experiment, a by-product is possibly produced...
in nitration of methyl benzoate, The reactive site on methyl benzoate obtains a ____________ hybridization after the initial addition