in nitration of methyl benzoate, The reactive site on methyl benzoate obtains a ____________ hybridization after the initial addition
answer : SP3 hybridization
in nitration of methyl benzoate, The reactive site on methyl benzoate obtains a ____________ hybridization after...
The reactive site on methyl benzoate obtains a ____________ hybridization after the initial addition. (The reaction is nitration of methyl benzoate.) A. sp3 B. sp2 C. sp3d D. sp E. sp3d2
For the nitration of methyl benzoate, draw the sigma complex (the reactive intermediate) which results from attack at the ortho, the meta, and the para positions. For each sigma complex, draw all appropriate resonance structures. Circle any "high energy'' resonance structures.
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
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.)
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.
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.
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....
Find the limiting reagent for the nitration of methyl benzoate.? Then calculate the percent yield I used Methyl benzoate - 2.3mL 15M HNO3- 3mL 18M H2SO4- 3mL Yield of crude product- 2.62g Yield of recrystalized product 1.89g