Good evening! There is my experimetal procedure for synthesis of bonzocaine: 12 ml of ethanol and...
Good evening!
There is my experimetal procedure for synthesis of bonzocaine:
12 ml of ethanol and 1.2 g of p-aminobenzoic acid was added and stirred until dissolving after 1 ml of conc. H2SO4 was added. Then it was heated under reflux for 40 minutes and cooled, next the mixture was transferred into 250 ml flask with 30 g of ice and 30 ml of water and 10 ml of 10% sodium bicarbonate solution was added until a pH of 8 was reached. Precipitate was collected by vacuum filtration.
And now I should calculate the yield.
Yield = actual yield which is actual mass of product / expected yield which is expected mass of product x 100%, actual yield is the mass of obtained product by filtration but how can I obtain the EXPECTED yield?
Thanks a lot for help!
Homework Answers
Add Answer to:
Good evening!
There is my experimetal procedure for synthesis of
bonzocaine:
12 ml of ethanol and...
Hello everyone! I am sorry in advance for so many questions. There is experimental procedure for...
Hello everyone! I am sorry in advance for so many questions. There is experimental procedure for benzocaine synthesis from p-aminobenzoic acid: 12 ml of ethanol and 0.9 g of p-aminobenzoic acid was added and stirred until dissolving after 1 ml of conc. H2SO4 was added. Then it was heated under reflux for 40 minutes and cooled, next the mixture was transferred into 250 ml flask with 30 g of ice and 30 ml of water and 10 ml of 10%...
EXPERIMENT XVII - SYNTHESIS OF BENZOCAINE Benzocaine is prepared by the of a carboxylic acid with...
AAnswer supplementary questions:
1 to 3
EXPERIMENT XVII - SYNTHESIS OF BENZOCAINE Benzocaine is prepared by the of a carboxylic acid with cthanol. The reaction is: 0 OCH2CH3 + CH CH OH NH NH and Non-Standard Equipment Chemicals absolute ethanol vacuum filter set-up stirring bans concentrated sulfuric acid boiling stones litmus paper 10% sodium carbonate Procedure Dissolve 1.2 g of p-aminobenzoic acid and 12 mL of absolute ethanol in a 100 mL round bottom flask. While swirling, add 1.0 mL...
are there any synthetic transformations produced in this lab Step 1. Preparation and Recrystallization of a...
are there any synthetic transformations produced in this
lab
Step 1. Preparation and Recrystallization of a Diastereomeric Salt - Synthesis of (R,R)-1,2-Diammoniumcyclohexane mono-(+)-tartrate: In a 150 ml beaker, L-(+)-Tartaric acid (7.5 g, 0.05 mol) is dissolved in 25 mL of distilled water. The solution is stirred as 11.4 g (12.2 mL, 0.10 mol) of 1,2-diaminocyclohexane is added carefully in one portion. (The addition of the diamine is exothermic.) A slurry is formed initially but complete dissolution is observed once addition...
using the procedure above complete the stoichiometry table Procedure In an oven-dried, 100 ml round bottom...
using the procedure above complete the stoichiometry
table
Procedure In an oven-dried, 100 ml round bottom flask containing magnetic stirring bar was added hydrobenzoin (1.0 8.4.7 mmol), anhydrous iron(III) chloride (0.3 g, 1.8 mmol), and anhydrous acetone (30 ml). The mixture was heated to reflux and stirred for 30 min. The reaction mixture was cooled tort and transferred to a separatory funnel containing 10% aq potassium carbonate (10 mL). Water (50 mL) was added and the aqueous solution was extracted...
Procedure: Measure and dispense 0.6 ml of a 4.4 M otion of sodium methoxide in methanol...
Procedure: Measure and dispense 0.6 ml of a 4.4 M otion of sodium methoxide in methanol and me of ethanol into a 5 mL reaction vial. Add 2.5 mmol of acetaminophen (40.378. Set up for reflux in the rume hood and bring reaction to reflux for 15 minutes (solvent is boiling and vapors are condensing condenser). After 15 minutes, directly through the top of the condenser tube, carefully add 0.3 ml of iemy iodide. Continue to reflux for another 45...
Can you explain how to find what is the theoretical yield, and the desired percent yield...
Can you explain how to find what is the theoretical yield, and
the desired percent yield of ethyl 4-nitrobenzoate?
1. Synthesis of ethyl 4-nitrobenzoate a) In a 50-ml round-bottom flask, weigh out 4-nitrobenzoic acid (0.85 g, 0.005 mol). Add to this 8 ml of absolute ethanol. Add boiling stones, and then bring this solution to the Lab Technologist. WATER OUT b) The Lab Technologist will deliver 1.2 ml of concentrated sulfuric acid to the mixture from the automatic pipette. [CAUTION,...
can you help answer this question according to the two other pictures? Procedure: Measure and dispense...
can you help answer this question according to the two other
pictures?
Procedure: Measure and dispense 0.6 ml of a 4.4 M solution of sodium methoxide in methanol and of ethanol into a 5 mL reaction vial. Add 2.5 mmol of acetaminophen (-0.378. Set up for reflux in the rume hood and bring reaction to reflux for 15 minutes (solvent is boiling and vapors are condensing on condenser). After 15 minutes directly through the top of the condenser tube, carefully...
5.0 ml of 2-methylcyclohexanol was placed in a 50 ml round bottom flask. Phosphoric acid (85%,...
5.0 ml of 2-methylcyclohexanol was placed in a 50 ml round bottom flask. Phosphoric acid (85%, 5 ml) was added cautiously, and the mixture swirled. Boiling stones were added to prevent bumping during heating. The mixture was heated to reflux temperature and refluxed for 15 minutes. The products were collected between 85-90 ˚C, in a small round bottom flask, cooled in ice water. Isolation Procedure The distillate was washed with 2 x 5 ml saturated sodium chloride solution in a...
SYNTHESIS OF trans-p-ANISALACETOPHENONE Prepare a table of all chemicals used in the procedure with their purpose...
SYNTHESIS OF trans-p-ANISALACETOPHENONE
Prepare a table of all chemicals used in the procedure with
their purpose
Melting point of trans-p-anisalacetophenone (with source) and
Molar mass of trans-p-anisalacetophenone (with source) (i cant find
these two things anywhere)
Procedure: 1. Carefully measure 1.0 mL each of p-anisaldehyde and acetophenone and place them in a screw-cap testtube. 2. To this add 3.0 mL of 95% ethanol. Shake the test tube gently to achieve a homogenous mixture. 3. Add 6-7 drops of 40% sodium...
number 5 please EXPERIMENT 8: BROMINATION OF TRANS-STILBENE glacial acetic acid Objective: Execute first step of...
number
5 please
EXPERIMENT 8: BROMINATION OF TRANS-STILBENE glacial acetic acid Objective: Execute first step of two-step sequence to transform an alkene into an alkyne via a dihalide intermediate and use infrared spectroscopy to identify functional groups 5. Identify the limiting reagent for the reaction and explain why it is the limiting reagent. PLEASE NOTE: You will need to draw out a Table of Reagents in your notebook to ensure that you know how many moles of each reagent you...
AAnswer supplementary questions:
1 to 3
EXPERIMENT XVII - SYNTHESIS OF BENZOCAINE Benzocaine is prepared by the of a carboxylic acid with cthanol. The reaction is: 0 OCH2CH3 + CH CH OH NH NH and Non-Standard Equipment Chemicals absolute ethanol vacuum filter set-up stirring bans concentrated sulfuric acid boiling stones litmus paper 10% sodium carbonate Procedure Dissolve 1.2 g of p-aminobenzoic acid and 12 mL of absolute ethanol in a 100 mL round bottom flask. While swirling, add 1.0 mL...
are there any synthetic transformations produced in this
lab
Step 1. Preparation and Recrystallization of a Diastereomeric Salt - Synthesis of (R,R)-1,2-Diammoniumcyclohexane mono-(+)-tartrate: In a 150 ml beaker, L-(+)-Tartaric acid (7.5 g, 0.05 mol) is dissolved in 25 mL of distilled water. The solution is stirred as 11.4 g (12.2 mL, 0.10 mol) of 1,2-diaminocyclohexane is added carefully in one portion. (The addition of the diamine is exothermic.) A slurry is formed initially but complete dissolution is observed once addition...
using the procedure above complete the stoichiometry
table
Procedure In an oven-dried, 100 ml round bottom flask containing magnetic stirring bar was added hydrobenzoin (1.0 8.4.7 mmol), anhydrous iron(III) chloride (0.3 g, 1.8 mmol), and anhydrous acetone (30 ml). The mixture was heated to reflux and stirred for 30 min. The reaction mixture was cooled tort and transferred to a separatory funnel containing 10% aq potassium carbonate (10 mL). Water (50 mL) was added and the aqueous solution was extracted...
Procedure: Measure and dispense 0.6 ml of a 4.4 M otion of sodium methoxide in methanol and me of ethanol into a 5 mL reaction vial. Add 2.5 mmol of acetaminophen (40.378. Set up for reflux in the rume hood and bring reaction to reflux for 15 minutes (solvent is boiling and vapors are condensing condenser). After 15 minutes, directly through the top of the condenser tube, carefully add 0.3 ml of iemy iodide. Continue to reflux for another 45...
Can you explain how to find what is the theoretical yield, and
the desired percent yield of ethyl 4-nitrobenzoate?
1. Synthesis of ethyl 4-nitrobenzoate a) In a 50-ml round-bottom flask, weigh out 4-nitrobenzoic acid (0.85 g, 0.005 mol). Add to this 8 ml of absolute ethanol. Add boiling stones, and then bring this solution to the Lab Technologist. WATER OUT b) The Lab Technologist will deliver 1.2 ml of concentrated sulfuric acid to the mixture from the automatic pipette. [CAUTION,...
can you help answer this question according to the two other
pictures?
Procedure: Measure and dispense 0.6 ml of a 4.4 M solution of sodium methoxide in methanol and of ethanol into a 5 mL reaction vial. Add 2.5 mmol of acetaminophen (-0.378. Set up for reflux in the rume hood and bring reaction to reflux for 15 minutes (solvent is boiling and vapors are condensing on condenser). After 15 minutes directly through the top of the condenser tube, carefully...
SYNTHESIS OF trans-p-ANISALACETOPHENONE
Prepare a table of all chemicals used in the procedure with
their purpose
Melting point of trans-p-anisalacetophenone (with source) and
Molar mass of trans-p-anisalacetophenone (with source) (i cant find
these two things anywhere)
Procedure: 1. Carefully measure 1.0 mL each of p-anisaldehyde and acetophenone and place them in a screw-cap testtube. 2. To this add 3.0 mL of 95% ethanol. Shake the test tube gently to achieve a homogenous mixture. 3. Add 6-7 drops of 40% sodium...
number
5 please
EXPERIMENT 8: BROMINATION OF TRANS-STILBENE glacial acetic acid Objective: Execute first step of two-step sequence to transform an alkene into an alkyne via a dihalide intermediate and use infrared spectroscopy to identify functional groups 5. Identify the limiting reagent for the reaction and explain why it is the limiting reagent. PLEASE NOTE: You will need to draw out a Table of Reagents in your notebook to ensure that you know how many moles of each reagent you...
Most questions answered within 3 hours.
-
38%
of adults say cashews are their favorite kind of nut. You
randomly select 12 adults...
asked 1 hour ago -
Notational Inc. is considering installing a new server. The
machine costs $100,000 and is expected to...
asked 1 hour ago -
Given the information coding of DNA strand:
5'-TTT-TAC-GAA-GAG-TGA-3',
Write the corresponding DNA template and mRNA strand...
asked 1 hour ago -
2. Boris recently synthesized an explosive compound he named
Badenoughium. The molecular formula for Bdenoughium is...
asked 5 hours ago -
5. A car decelerate evenly from a velocity of 50mph until rest
in a distance of...
asked 5 hours ago -
IN HTML Programming
1. Write a script that inputs integers (one at a time) and
passes...
asked 5 hours ago -
A dentist uses a mirror to examine a tooth that is 0.75 cm in
front of...
asked 5 hours ago -
You set up a 100,000 line of credit for the business on 1/1/X8,
annual interest is...
asked 5 hours ago -
What is the measurement uncertainty of a pan balance? How did you
get that?
asked 5 hours ago -
Suppose four firms have market shares of 30%, 30%, 20% and 20%.
What is the Herfindahl-Hirschman...
asked 6 hours ago -
IBT Industrial Solutions produces forty units of rack and pinion
type steering gears during an eight...
asked 6 hours ago -
The Ksp for PbI2 is 9.8×10−9 . Will PbI2 precipitate if 2.5 mL
of 0.0025 M...
asked 6 hours ago