In the nitration of methyl benzoate, an excess of nitric acid is used. Explain why the...
nitration of methyl benzoate why is the reaction mixture cooled as the sulfuric/nitric acid mixture is added?
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 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
Consider the nitration of methyl benzoate by concentrated nitric and sulfuric acids via an electrophilic aromatic substitution to form methyl m-nitrobenzoate. Calculate the molar masses of the reactants and product. Consider the nitration of methyl benzoate by concentrated nitric and sulfuric acids via an electrophilic aromatic substitution to form methyl m-nitrobenzoate Calculate the molar masses of the reactants and product. O. conc. HNO3, conc. H2SO4 TE: hydrogens have been omitted for clarity. O2 Report molar masses to 1 decimal place....
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
-NITRATION OF Methyl benzoate -addditional information. .( 3.9 g of the product methyl 3-nitrobenzoate for the percentage yield Materials used: Amount Compound used/ Molecular weight Density (g/mL) Moles produced 3.05g used 136.15 g/mol N/A 0.0224 mol Methyl Benzoate HO-S-OH 6mL used 98.079 g/mol 1.83 g/cm3 0.112 Sulfuric Acid 2mL used 63.01 g/mol 1.51 g/cm3 0.047g o-N-OH Nitric Acid 3.034g of pure product 181.15 g/mol produced N/A 0.0167 mol NO2 Methyl-m- nitrobenzoate Calculating limiting reagent and theoretical yield: 0.0224 mol methylbenzoate...
Draw the reaction mechanism for the nitration of methyl benzoate to methyl nitrobenzoate, please show all resonance structures for each possible substitution position to explain why methyl m-nitrobenzoate was the favored isomer.
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.
Nitration of Methyl Benzoate to synthesize Methyl m-nitrobenzoate Find theoretical yield and percent yield. Show all steps. Results: .040 g of methyl m-nitrobenzoate crystals produced 1. Add .30 g of Methyl Benzoate to .6 ml of Sulfuric Acid in a reaction tube 2. Dropwise add a mixture of .2 ml of sulfuric acid and .2ml of nitric acid 3. After 15 min, pour onto 2.5 g of ice in a small beaker 4. Use suction filtration to dry crystals. Wash...
acid base reaction (with mechanism showing arrows) for the nitration of methyl benzoate experiment. (An electophilic aronatic substition reastion)