Complete the table of reactants and products for the following two reactions.
| Compound | Molar Mass (g/mol) | Mass | Volume | Density (g/mL) | # Mols | Equivalents of Reactants (divide actual moles by stoichiometric moles) | Other (indicate which is limiting reactant) |
|---|---|---|---|---|---|---|---|
Nitration of Methyl Benzoate
In a 50 mL Erlenmeyer flask, cool 6 mL of conc. H2SO4 in ice and add 3.0 g of methyl benzoate. Make sure the temperature stays at 0 oC . Using a pipet, slowly add a cooled mixture of 2 mL of conc. HNO3 and 2 mL of conc. H2SO4. During the addition, swirl the flask to mix the reagents and keep it in an ice bath to ensure that the reaction mixture stays below 15 oC. When the addition is complete, remove the reaction mixture from the ice bath and allow it to stand at room temperature for 20 min. with occasional stirring. Pour the solution directly over about 25 g of ice in a beaker and collect the formed crystals by vacuum filtration. Wash the crystals with two 5 mL portions of ice cold water, then two 5 mL portions of ice cold methanol.
Nitration of Acetanilide
Add 2.5 mL of conc. H2SO4 and 1.0 g of acetanilide to a 25 mL Erlenmeyer flask. Swirl the contents of the flask until the solid dissolves. Make sure the temperature of the mixture never exceeds 25 oC. Cool the reaction mixture in an ice bath to 5-10 oC. Prepare a solution of 2 mL of conc. HNO3 and 2 mL of conc. H2SO4 and cool it. Add the acid solution dropwise to the cooled acetanilide in the 25 mL Erlenmeyer flask over about 15 min. Be careful not to let the temperature of the solution exceeds 25 oC or product will be lost. When addition is complete, allow the reaction mixture to stand at room temperature for 20 min. with occasional stirring. Pour the mixture into a beaker containing about 50 mL of water and 15-20 g of ice. Collect the precipitate via vacuum filtration and wash it with two 5 mL portions of ice cold water.
Complete the table of reactants and products for the following two reactions. Compound Molar Mass (g/mol)...
For the nitration of methyl benzoate:
a. Which product did you get? What evidence do you have for
this?
b. Was your product pure? What evidence do you have for this?
Explain your evidence.
c. Draw the mechanism for the product you got.
For the bromination of acetanilide:
a. Which product did you get? What evidence do you have for
this?
b. Was your product pure? What evidence do you have for this?
Explain your evidence.
c. Draw the mechanism...
numbers 1-3
Post-Laboratory Questions-EXP 3 Nitration of Aromatic Compounds Name: Due after completing the lab. 1. Why is concentrated sulfuric acid emploved in thie on? What is the electrophile that is produced by the reaction of sulfuric acid and nitric acid? 2. Why is it important to maintain the reaction temperature low and the addition of nitric acid-sulfuric acid mixture carried out slowly? 3. Explain why concentrated H2SO4, not concentrated HC1, was used in this experiment? 4. Which ring of...
Calculate the quantity (mmol) of reagents to be used in the
assigned experiment. Which reagent is the limiting reagent? Show by
calculations.
8. n the reaction of vanillin with silver oxide, what gets oxidized and what gets reduced? Part B: Miniscale Hydrolysis of Methyl Salicylate To a 25-mL round-bottom flask containing a spin bar, add 7.5 mL of 5 M NaOH and 1.0mL. of methyl salicylate. Swirl to mix. A white solid will form, which will eventually disap- pear as...
3-5 pls
Post-Laboratory Questions-EXP 3 Nitration of Aromatic Compounds Name: Due after completing the lab. 1. Why is concentrated sulfuric acid employed in this reaction? What is the electrophile that is produced by the reaction of sulfuric acid and nitric acid? 2. Why is it important to maintain the reaction temperature low and the addition of nitric acid-sulfuric acid mixture carried out slowly? 3. Explain why concentrated H2SO, not concentrated HCl, was used in this experiment? 4. Which ring of...
1. Explain why the nitration of methylbenzoate occurs in the meta position 2. Why is it important to a synthesis reaction of m-nitromethylbenzoate mixute to be cold? 3. What is the function of sulfuric acid in this synthesis These are the procedures for reference Procedure: Add concentrated Sulfuric acid to a conical vial (CV) to the 0.3 mL line. Perform in a fume hood. Cool the CV in an ice bath to 0-10 oC and then add 0.140 mL of...
the
weight if the initial product was 3.4 grams of methyl
benzoate.
Who |o yald foR 3.91SSg st prodoct nd product 2.14143 EXPERIMENTAL PROCEDURE SAFETY WEAR nitrile gloves for this experiment. The nitrating moture of sulfuric acidnitric acid (1:1) is a very strong acid system. Do not allow it to come in contact with your skin or clothing. It will cause acid burns if it comes in contact with your skin (and holes an your clothes). Wash any affected area...
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...
Bromination of Acetanilide In a 25-mL Erlenmeyer flask, dissolve 0.68 g of acetanilide in approximately 4 mL glacial acetic acid. Record the exact amount of the limiting reactant that you used. Add a stir bar followed by 1.6 g pyridinium tribromide. Heat the mixture to ~60°C in a warm water bath for 10 minutes. After the 10 minutes, add 15 mL water and approximately 2 mL saturated sodium bisulfite solution to remove excess bromine, which shows by the disappearance of...
how do I get the molar ratios between NaBr, 1-butanol
and H2SO4 used in the experiment sn2 reaction 1-bromobutane
Moles:
NaBr: 0.0275
Butanol: 0.0216
H2SO4: 0.00840
butanol is the limiting reagent
Experiment: 08 The S2 Reaction: 1-Bromobutane Substitution nucleophilic bimolecular (SN2) reactions can be utilized to convert primary alcohols to corresponding halogens. In this experiment, 1-butanol is treated with a nucleophile (Br) to generate the corresponding 1-bromobutane. The nucleophile in this lab is generated from an aqueous solution of NaBr....
used. Experimental . Place 2.0 g of salicylic acid in a 125-mL conical flask. 2. Add 4.0 ml (d = 1.08 g/mL; 4.3 g) of acetic anhydride and 6-8 drops of 85% phosphoric acid. 3. Swirl the flask to mix all reagents, and place it in a 70°C water bath. Heat for about 10 minutes. 4. Remove the flask from the water bath and add 2 mL of cold water drop- wise, swirling the flask after each addition, 5. Add...