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QUESTIONS 1. Why does methyl benzoate dissolve in concentrated sulfuric acid? 2. What is the EQUATION...
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.
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....
nitration of methyl benzoate why is the reaction mixture cooled as the sulfuric/nitric acid mixture is added?
What would be the theoretical yield of reacting methyl benzoate (C₆H₅CO₂CH3) with nitric acid (HNO3) and sulfuric acid (H2SO4), producing methyl m-nitrobenzoate (C6H4CO2CH3NO2)? 6 g methyl benzoate 4 mL nitric acid 4 mL sulfuric acid crude methyl m-nitrobenzoate recovered: 7.260 g pure methyl m-nitrobenzoate recovered: 6.227 g
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
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?...
In the nitration of methyl benzoate, an excess of nitric acid is used. Explain why the reaction stops at the single nitration and does not go on further to the double nitration.
Show the detailed mechanism of the formation of methyl orange from 4- diazobenzenesulfonic acid and N,N-dimethylaniline. Show the detailed mechanism of the formation of methyl orange from 4-diazobenzenesulfonic acid and N, N dimethy laniline. What is the name of this mechanism? What is the name of the organic functional group formed in this reaction? What is the name of this reaction? Why does the coupling occur at the para position of the N, N-dimethylaniline? What prevents the reaction from occurring...
orgo 2 ex.. Search References Mailings Review View Help 1. What is the balanced equation for the preparation of aspirin? 2. What type of reaction is this? 3. Describe the purity of your product based on its melting point range and its appearance. What is the position of the O-H stretch in the IR spectrum? 4. Why is concentrated phosphoric acid added? Concentrated sulfuric acid may be used in place of the phosphoric acid, but HCL La volatile substrate) and...
help with 3 and 4 on from risic vent for the ons formed POSTLAB QUESTIONS 1. Sulfuric acid serves three functions in this action: 1) in the format dcia; 2) as the Lewis acid catalyst for electrophilic aromatic substituto reaction by dissolving the methul benzoate. Based on the procond explain why nitration occurs primarily at the meta position and no 2. What two techniques were used in this experiment to prevent dinica 3. What would be the structure of the...