Why in the nitration of naphthalene does the product 1-nitronaphthalene make more product than 2-nitronaphthalene. Please explain.
Why in the nitration of naphthalene does the product 1-nitronaphthalene make more product than 2-nitronaphthalene. Please...
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?...
Answer both please Why does fluorenone travel more slowly than fluorene? Why does acetone speed up the rate at which fluorenone travels? (Make sure to include a picture of your TCL plate in your lab report)
!. Why does it make sense that tRNA and rRNA molecules are more stable than mRNA molecules? 2. What is meant by the genetic code being universal and redundant?
Nitration of phenols is a classic example of an electrophilic aromatic substitution reaction. a) Why does the nitration of phenol (hydroxybenzene) proceed only in the ortho- and para-positions on the ring? b) Draw the resonance structures that highlight the ortho- and para-directing nature of hydroxy substituents. Make sure to include the structures that showcase the movement of the charges in the ring.
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...
Explain in detail why does bromination of ethoxy benzene occur more rapidly than phenyl benzoate? Please illustrate also.
please explain 1. Why is the conjugate base of aspirin more soluble in water than ether? 2. Why does the extraction of aspirin by NaHCO3 generate a gas? 3. Assume 1 g of the 3 g is aspirin. Show by calculation that 7 mL of 6 M HCI is enough to completely neutralize the conjugate base of aspirin to the neutral compound.
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.
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.
1. Why does comparative advantage matter more than absolute advantage for trade? 2. Draw a production possibilities frontier curve. Illustrate the set of points that is feasible, the set of points that is efficient, the set of points that is inefficient, and the set of points that is not feasible. If you prefer not to draw then explain. 3. Explain why seniors often earn lower grades in their last semester before graduation (hint: incentive problem).