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2. Complete the reaction for the nitration of acetanilide. HN p-nitroacetanilide
What products may form if the EAS reaction of acetanilide to form o-nitroacetanilide & p-nitroacetanilide is...
What products may form if the EAS reaction of acetanilide to form o-nitroacetanilide & p-nitroacetanilide is not performed correctly? A) 2,3,4,5,6-pentanitroacetanilide B) 2,4-dinitroacetanilide C) 2,4,6-trinitroacetanilide D) 3,4-dinitroacetanilide E) Both 2,4-dinitroacetanilide and 2,4,6-trinitroacetanilide are possible
Calculate the theoretical yield for p-nitroacetanilide (assume that all of the acetanilide would react to form...
Calculate the theoretical yield for p-nitroacetanilide (assume that all of the acetanilide would react to form p-nitroacetanilide). (for Electrophilic Aromatic Substitution: Preparation of p-Nitroacetanilide experiment). The weight of acetanilide is 1.0 g.
What products may form if the EAS reaction of acetanilide to form p-nitroacetanilide is not performed...
What products may form if the EAS reaction of acetanilide to form p-nitroacetanilide is not performed correctly? A) 2,3,4,5,6-pentanitroacetanilide B) 2,4-dinitroacetanilide C) 2,4,6-trinitroacetanilide D) 3,4-dinitroacetanilide E) Both 2,4-dinitroacetanilide and 2,4,6-trinitroacetanilide are possible
Organic Chemistry Nitration lab. 1. Aromatic nitration requires the use of the HNO3 / H2SO4 mixture....
Organic Chemistry Nitration lab. 1. Aromatic nitration requires the use of the HNO3 / H2SO4 mixture. Why not use HNO3 alone? 2. Why should the cold nitration reaction be maintained at all times? 3. What difference should be observed between the 1 H NMR spectrum of the nitrated reagent and the product obtained? Explain 4. If the yield percentages for acetanilide nitration products were: 35% o-nitroacetanilide and 65% p-nitroacetanilide, explain how you would perform the procedure to separate and recover...
Draw the resonance forms for the arenium ion formed during the reaction of nitrating acetanilide (nitroacetanilide).
Draw the resonance forms for the arenium ion formed during the reaction of nitrating acetanilide (nitroacetanilide).
Post Lab Questions for Nitration of Acetanilide, Nitration of Methyl Benzoate, Nitration of Phenylacetonitrile, Nitration of...
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?...
Acetanilide, which has a molar mass of 135.17 g/mol, can be nitrated to nitroacetanilide, which has...
Acetanilide, which has a molar mass of 135.17 g/mol, can be nitrated to nitroacetanilide, which has a molar mass of 180.16 g/mol, by the addition of nitric acid. What is the theoretical yield (in g) of the mononitrated product, nitroacetanilide, from 0.499 g of acetanilide?
Acetanilide, which has a molar mass of 135.17 g/mol, can be nitrated to nitroacetanilide, which has...
Acetanilide, which has a molar mass of 135.17 g/mol, can be nitrated to nitroacetanilide, which has a molar mass of 180.16 g/mol, by the addition of nitric acid. What is the theoretical yield (in g) of the mononitrated product, nitroacetanilide, from 0.503 g of acetanilide? Answer:
In nitration of acetanilide(synthesis of p-nitroaniline) main product is ortho and para. Explain why ortho and...
In nitration of acetanilide(synthesis of p-nitroaniline) main product is ortho and para. Explain why ortho and para product is major in resonance and mechanism term.
Which compound should have the highest Rf value on a TLC plate? A acetanilide B nitroacetanilide...
Which compound should have the highest Rf value on a TLC plate? A acetanilide B nitroacetanilide C dinitroacetanilide
Organic Chemistry Nitration lab. 1. Aromatic nitration requires the use of the HNO3 / H2SO4 mixture. Why not use HNO3 alone? 2. Why should the cold nitration reaction be maintained at all times? 3. What difference should be observed between the 1 H NMR spectrum of the nitrated reagent and the product obtained? Explain 4. If the yield percentages for acetanilide nitration products were: 35% o-nitroacetanilide and 65% p-nitroacetanilide, explain how you would perform the procedure to separate and recover...
Acetanilide, which has a molar mass of 135.17 g/mol, can be nitrated to nitroacetanilide, which has a molar mass of 180.16 g/mol, by the addition of nitric acid. What is the theoretical yield (in g) of the mononitrated product, nitroacetanilide, from 0.503 g of acetanilide? Answer:
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