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Name Experiment 7 - PREPARATION OF ASPIRIN AND OTHER ESTERS Date Partner Station # - Pre-Lab...
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...
Chemistry 172 pre-lab questions 1. ch aspirin was made from a lab experiment. Preparation of Aspirin...
Chemistry 172 pre-lab questions 1. ch aspirin was made from a lab experiment. Preparation of Aspirin A student would like to determine how much aspirin was made from The following is the lab data: Mass of flask 73.86 g Mass of flask & salicylic acid 77.88 g Mass of salicylic acid 4.02 g Mass of watch glass + filter paper 34.63 Mass of watch glass, filter paper & aspirin 38.29 g a. How much aspirin was made? b. The mass...
Carboxylic Acids and Esters EXPERIMENT 22 OBSERVATIONS AND RESULTS Synthesis and Identification of an Ester: Esterification...
Carboxylic Acids and Esters EXPERIMENT 22 OBSERVATIONS AND RESULTS Synthesis and Identification of an Ester: Esterification 1. Give the name and structure of the ester which you synthesized. What fruit did you associate with the odor of the ester? to noldsoinogs w to esar bnn eaman sd vio stolpi Look up the ester and its fruit sburce in your textbook. (If it is not in your textbook, ask your instructor.) Did you associate the ester with the right fruit? If...
find the theoretical yield of the acetysalicylic acid . EXPERIMENT 19 PREPARATION OF ASPIRIN In addition...
find the theoretical yield of the acetysalicylic acid .
EXPERIMENT 19 PREPARATION OF ASPIRIN In addition to the Fischer esterification method presented in Experiment 18, a second method for preparation of esters involves the reaction of anhydrides with the hydroxyl This method is ospecialy usoful for tho preparation of acetate esters, since acetic anhydride is an inexpensive and reactive reagent. In this experiment the hydroxyl group of salicylic acid is acetic anhydride to make acetylsalicylic acid, or aspirin. The short...
- OF ASPIRIN ANU UN riment Exercise 7: The Yield of Aspirin Name Date Pred the...
- OF ASPIRIN ANU UN riment Exercise 7: The Yield of Aspirin Name Date Pred the el the st 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 videos 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...
Problem Set 7 Stoichiometry Calculations Name: Date: Lab Section: General Instructions: Complete the following problems, Circle...
Problem Set 7 Stoichiometry Calculations Name: Date: Lab Section: General Instructions: Complete the following problems, Circle answers and show all work on separate sheet(s) of paper. 5 problems will be chosen randomly for assessing a score on this assignment. Assignment is due at the end of the lab period. 1.) 5.0 g of magnesium metal is burned in excess oxygen to produce magnesium oxide. (a) Write a balanced chemical equation for this reaction with the correct phases of all substances...
PRE-LAB QUIZ for EXPERIMENT 27 Name 1. In Experiment 27, a modified Perkin reaction is performed....
PRE-LAB QUIZ for EXPERIMENT 27 Name 1. In Experiment 27, a modified Perkin reaction is performed. The Perkin reaction is a carbonyl condensation reaction that is related to the Claisen condensation and aldol condensation. In this experiment, the reactants are benzaldehyde and 3-benzoylpropionic acid with sodium acetate and acetic anhydride as catalysts. Draw the structures of these compounds in the space below. benzaldehyde 3-benzoylpropionic acid acetic anhydride 2. The first step of the reaction is the formation of the mixed...
DUE TOMORROW!!! Name Lab Instructor Date SS is Just a Four Letter Word UUUUUUU Pre Lab Assignment Experiment 3: HES...
DUE TOMORROW!!!
Name Lab Instructor Date SS is Just a Four Letter Word UUUUUUU Pre Lab Assignment Experiment 3: HESS is Just a Four Le Consider the following reactions 1. CH(g) + 2 O2(g) - CO2(g) + 2 H20(1): AH=-890 kJ/mol 2. 2 CH (9) + 4 O2(g) – 2 CO2(g) + 4H2O(): AH=-1780 kJ/mo 3. CO2(g) + 2 H2O(l) - CHug) +2 02(g): AH=890 kJ/mol 4. 2 H2O(l) + 2 H2O(g): AH = 88 kJ/mol Quantitatively, how does the...
Pre-lab Questions: Importance A one-step preparation of aspirin from its precursor, salicylic acid, via an ester...
Pre-lab Questions:
Importance A one-step preparation of aspirin from its precursor, salicylic acid, via an ester formation illustrates one of synthetic organic chemistry's most important uses, making the drugs that treat all types of illnesses. OH HOOH Background Aspirin is a prodrug of salicylic acid, the actual active drug. A compound related to salicylic acid, salicin, was first isolated from willow bark in the mid 1700's, but willow-bark extract was used by the ancient Greeks as a treatment for pain...
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c)...
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
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...
Chemistry 172 pre-lab questions 1. ch aspirin was made from a lab experiment. Preparation of Aspirin A student would like to determine how much aspirin was made from The following is the lab data: Mass of flask 73.86 g Mass of flask & salicylic acid 77.88 g Mass of salicylic acid 4.02 g Mass of watch glass + filter paper 34.63 Mass of watch glass, filter paper & aspirin 38.29 g a. How much aspirin was made? b. The mass...
Carboxylic Acids and Esters EXPERIMENT 22 OBSERVATIONS AND RESULTS Synthesis and Identification of an Ester: Esterification 1. Give the name and structure of the ester which you synthesized. What fruit did you associate with the odor of the ester? to noldsoinogs w to esar bnn eaman sd vio stolpi Look up the ester and its fruit sburce in your textbook. (If it is not in your textbook, ask your instructor.) Did you associate the ester with the right fruit? If...
find the theoretical yield of the acetysalicylic acid .
EXPERIMENT 19 PREPARATION OF ASPIRIN In addition to the Fischer esterification method presented in Experiment 18, a second method for preparation of esters involves the reaction of anhydrides with the hydroxyl This method is ospecialy usoful for tho preparation of acetate esters, since acetic anhydride is an inexpensive and reactive reagent. In this experiment the hydroxyl group of salicylic acid is acetic anhydride to make acetylsalicylic acid, or aspirin. The short...
- OF ASPIRIN ANU UN riment Exercise 7: The Yield of Aspirin Name Date Pred the el the st 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 videos 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...
Problem Set 7 Stoichiometry Calculations Name: Date: Lab Section: General Instructions: Complete the following problems, Circle answers and show all work on separate sheet(s) of paper. 5 problems will be chosen randomly for assessing a score on this assignment. Assignment is due at the end of the lab period. 1.) 5.0 g of magnesium metal is burned in excess oxygen to produce magnesium oxide. (a) Write a balanced chemical equation for this reaction with the correct phases of all substances...
PRE-LAB QUIZ for EXPERIMENT 27 Name 1. In Experiment 27, a modified Perkin reaction is performed. The Perkin reaction is a carbonyl condensation reaction that is related to the Claisen condensation and aldol condensation. In this experiment, the reactants are benzaldehyde and 3-benzoylpropionic acid with sodium acetate and acetic anhydride as catalysts. Draw the structures of these compounds in the space below. benzaldehyde 3-benzoylpropionic acid acetic anhydride 2. The first step of the reaction is the formation of the mixed...
DUE TOMORROW!!!
Name Lab Instructor Date SS is Just a Four Letter Word UUUUUUU Pre Lab Assignment Experiment 3: HESS is Just a Four Le Consider the following reactions 1. CH(g) + 2 O2(g) - CO2(g) + 2 H20(1): AH=-890 kJ/mol 2. 2 CH (9) + 4 O2(g) – 2 CO2(g) + 4H2O(): AH=-1780 kJ/mo 3. CO2(g) + 2 H2O(l) - CHug) +2 02(g): AH=890 kJ/mol 4. 2 H2O(l) + 2 H2O(g): AH = 88 kJ/mol Quantitatively, how does the...
Pre-lab Questions:
Importance A one-step preparation of aspirin from its precursor, salicylic acid, via an ester formation illustrates one of synthetic organic chemistry's most important uses, making the drugs that treat all types of illnesses. OH HOOH Background Aspirin is a prodrug of salicylic acid, the actual active drug. A compound related to salicylic acid, salicin, was first isolated from willow bark in the mid 1700's, but willow-bark extract was used by the ancient Greeks as a treatment for pain...
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
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