Homework Answers
An
aqeous solution of HCl can be used to seperate them, Phenacetin
will be converted into its salt form by adding aq. HCl thus will be
soluble in aqeous fraction and asprin will be collected in
Chloroform fraction during extraction.
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QUESTION 7 A chloroform solution containing aspirin and phenacetin (structures shown below) is provided to you...
Solutions??? Lab Partner(s): Isolation of Active Ingredients of Excedrin-Week 1 Task A: Separate the mixture of...
Solutions???
Lab Partner(s): Isolation of Active Ingredients of Excedrin-Week 1 Task A: Separate the mixture of active ingredients of Excedrin from the exciplents in the toblet. 01. Complete the following flowchart. Based on step 1 you performed in the lab. Moture of aspirin, caffeine and acetaminophen along with insoluble excipients Solvent a itrate residue Q3. Based on step 2 you performed, complete the following flowchart to depict the scheme of separation of acetaminophen from insoluble excipients. Mixture of acetaminophen and...
Question 17 3 pts You need to separate dibenzyl amine from a mixture of organic compounds...
Question 17 3 pts You need to separate dibenzyl amine from a mixture of organic compounds dissolved in diethyl ether. Which aqueous solution would be most effective to do this via extraction? O 1M NaCIO 1MHCI Ο 1ΜΚΙ O 1M NaOH O 1M Naci
13. In step 5 of reaction 3, the reaction mixture containing the products shown below in...
13. In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice with HCI. NH2 NH HN o-methylaniline m-methylaniline p-methylacetanilide a) Which products (shown above) from reaction 3 can react with HCl in an acid-base reaction? Show the mechanism for this acid-base reaction and give the structures that would result from the protonation of these products. Which phase (organic or aqueous) would these protonated products be soluble in? (6 points) Reaction...
Exercise 7: The % Yield of Aspirin Name Date Read Exercise 7 in your lab manual....
Exercise 7: The % Yield of Aspirin Name Date Read Exercise 7 in your lab manual. Complete the Pre-lab Assignment. In this substitute lab exercise, you will watch a short video on preparing aspirin. The video is posted on the course Moodle page, and it provides the masses of the reactants and the product; you should be able to calculate the theoretical yield and the % yield from the data given by the video. Submit the completed assignment by March...
7. You make 1 Liter of an aqueous solution containing 9.20 ml of 57.8 mM acetic...
7. You make 1 Liter of an aqueous solution containing 9.20 ml of 57.8 mM acetic acid and 56.2 mg of sodium acetate (MW = 82.0 g/mole). a. How many moles of acetic acid did you add? b. How many moles of sodium acetate did you add? c. What is the appropriate formula for calculating the pH of the above solution? d. What is the pH of the above solution? Is it acidic or basic? Slightly or strongly so? (Use...
Extraction of solids: Experiment outlined below Draw a “roadmap” of the experiment, containing chemical structures and...
Extraction of solids: Experiment outlined below
Draw a “roadmap” of the experiment, containing chemical
structures and “layers” (organic and aqueous). This should contain
the individual reactions occurring in each step, and show which
layer the various components are present. Make sure you think about
whether the acetaminophen, caffeine and aspirin are neutral,
protonated or deprotonated.
Preliminary separation obtain a sample (1.0g) of the mixture. weigh the sample and record it. this sample should consist of a 2:1:1 mixture (by mass)...
Acid/Base Extraction 1. Provide a flow chart detailing the acid/base extraction/separation of the compounds shown below....
Acid/Base Extraction
1. Provide a flow chart detailing the acid/base
extraction/separation of the compounds shown below. Your answer
must employ the following reagents: methylene chloride,
hydrochloric acid (1M & 6M), sodium hydroxide (1M & 6M),
10% sodium bicarbonate (aq). Clearly indicate the product(s) and
layers formed following each step of your separation scheme.
IMPORTANT: p-cresol is soluble in sodium hydroxide solution but
insoluble in neutral water or sodium bicarbonate solution. 2-
ethylbenzoic acid is soluble in both sodium hydroxide and...
1. Using Sigma-Aldrich website or Merck Index website or Google search find and draw structures for...
1. Using Sigma-Aldrich website or Merck Index website or Google search find and draw structures for the following compounds. (a) Atropine (b) Hydroxychloroquine (c) Saccharin (d) Cholesterol (e) Vitamin C (ascorbic acid) 2. Find the melting points for the following compounds by using Sigma-Aldrich or Google search (a) Biphenyl (b) 4-bromobenzoic acid (C) 3-nitrophenol 9. Chlorine, bromine and iodine all react with alkenes such as ethene in an addition reaction (a) Write the equation for the bromination of ethene, and...
13. In step 5 of reaction 3, the reaction mixture containing the products shown below in...
13. In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice with HCI. NH2 NH2 HN o-methylaniline m-methylaniline p-methylacetanilide a) Which products (shown above) from reaction 3 can react with HCl in an acid-base reaction? Show the mechanism for this acid-base reaction and give the structures that would result from the protonation of these products. Which phase (organic or aqueous) would these protonated products be soluble in? (6 points) b)...
Acid/Base Extraction ACID/BASE EXTRACTION Provide a flow chart detailing the acid/base extraction/separation of the compounds shown...
Acid/Base Extraction
ACID/BASE EXTRACTION Provide a flow chart detailing the acid/base extraction/separation of the compounds shown below. Your answer must employ the following reagents: methylene chloride, hydrochloric acid (1M & 6M), sodium hydroxide (1M & 6M), 10% sodium bicarbonate (aq). Clearly indicate the product(s) and layers formed following each step of your separation scheme. HINT: phenol is soluble in sodium hydroxide solution but insoluble in neutral water or sodium bicarbonate solution. Benzoic acid is soluble in both sodium hydroxide and...
Solutions???
Lab Partner(s): Isolation of Active Ingredients of Excedrin-Week 1 Task A: Separate the mixture of active ingredients of Excedrin from the exciplents in the toblet. 01. Complete the following flowchart. Based on step 1 you performed in the lab. Moture of aspirin, caffeine and acetaminophen along with insoluble excipients Solvent a itrate residue Q3. Based on step 2 you performed, complete the following flowchart to depict the scheme of separation of acetaminophen from insoluble excipients. Mixture of acetaminophen and...
Question 17 3 pts You need to separate dibenzyl amine from a mixture of organic compounds dissolved in diethyl ether. Which aqueous solution would be most effective to do this via extraction? O 1M NaCIO 1MHCI Ο 1ΜΚΙ O 1M NaOH O 1M Naci
13. In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice with HCI. NH2 NH HN o-methylaniline m-methylaniline p-methylacetanilide a) Which products (shown above) from reaction 3 can react with HCl in an acid-base reaction? Show the mechanism for this acid-base reaction and give the structures that would result from the protonation of these products. Which phase (organic or aqueous) would these protonated products be soluble in? (6 points) Reaction...
Exercise 7: The % Yield of Aspirin Name Date Read Exercise 7 in your lab manual. Complete the Pre-lab Assignment. In this substitute lab exercise, you will watch a short video on preparing aspirin. The video is posted on the course Moodle page, and it provides the masses of the reactants and the product; you should be able to calculate the theoretical yield and the % yield from the data given by the video. Submit the completed assignment by March...
Extraction of solids: Experiment outlined below
Draw a “roadmap” of the experiment, containing chemical
structures and “layers” (organic and aqueous). This should contain
the individual reactions occurring in each step, and show which
layer the various components are present. Make sure you think about
whether the acetaminophen, caffeine and aspirin are neutral,
protonated or deprotonated.
Preliminary separation obtain a sample (1.0g) of the mixture. weigh the sample and record it. this sample should consist of a 2:1:1 mixture (by mass)...
Acid/Base Extraction
1. Provide a flow chart detailing the acid/base
extraction/separation of the compounds shown below. Your answer
must employ the following reagents: methylene chloride,
hydrochloric acid (1M & 6M), sodium hydroxide (1M & 6M),
10% sodium bicarbonate (aq). Clearly indicate the product(s) and
layers formed following each step of your separation scheme.
IMPORTANT: p-cresol is soluble in sodium hydroxide solution but
insoluble in neutral water or sodium bicarbonate solution. 2-
ethylbenzoic acid is soluble in both sodium hydroxide and...
1. Using Sigma-Aldrich website or Merck Index website or Google search find and draw structures for the following compounds. (a) Atropine (b) Hydroxychloroquine (c) Saccharin (d) Cholesterol (e) Vitamin C (ascorbic acid) 2. Find the melting points for the following compounds by using Sigma-Aldrich or Google search (a) Biphenyl (b) 4-bromobenzoic acid (C) 3-nitrophenol 9. Chlorine, bromine and iodine all react with alkenes such as ethene in an addition reaction (a) Write the equation for the bromination of ethene, and...
13. In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice with HCI. NH2 NH2 HN o-methylaniline m-methylaniline p-methylacetanilide a) Which products (shown above) from reaction 3 can react with HCl in an acid-base reaction? Show the mechanism for this acid-base reaction and give the structures that would result from the protonation of these products. Which phase (organic or aqueous) would these protonated products be soluble in? (6 points) b)...
Acid/Base Extraction
ACID/BASE EXTRACTION Provide a flow chart detailing the acid/base extraction/separation of the compounds shown below. Your answer must employ the following reagents: methylene chloride, hydrochloric acid (1M & 6M), sodium hydroxide (1M & 6M), 10% sodium bicarbonate (aq). Clearly indicate the product(s) and layers formed following each step of your separation scheme. HINT: phenol is soluble in sodium hydroxide solution but insoluble in neutral water or sodium bicarbonate solution. Benzoic acid is soluble in both sodium hydroxide and...
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