Homework Answers
Fluorene percentage = (201 mg / 537 mg) x 100 = 37.4 %
Benzoic acid percentage = (242 mg / 537 mg) x 100 = 45.06 %
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A 537 mg of a mixture of fluorene and benzoic acid was weighed...
A 577 mg of a mixture of fluorene and benzoic acid was weighed out and subjected...
A 577 mg of a mixture of fluorene and benzoic acid was weighed out and subjected to an extraction and recrystallization. After this purification was completed the product crystals were dried and analyzed. The purification procedure produced 247 mg of fluorene and 167 mg of benzoic acid. Calculate the percent composition of this mixture. Fluorene Benzoic Acid Number Number 0 0
separation of a three-component mixture by extraction, lab report help, the compounds are benzoic acid ,9-fluorene...
separation of a three-component mixture by extraction, lab report help, the compounds are benzoic acid ,9-fluorene , and ethyl-4- aminobenzoate. I need help to write Discussion about this lab report and I dont know what should I write.I got 25% recovary for benzoic acid ,32% for ethyl-4- aminobenzoate and 50 % recovary for 9-fluorene.( by the way I lost some product of benzoic acid). please help me full paper as you could for discussion and what is the source of...
You weight out exactly 1.00 mg of benzoic acid and dissolve it in a mixture of...
You weight out exactly 1.00 mg of benzoic acid and dissolve it in a mixture of 2.0 mL of diethyl ether and 2.0 mL of water. After mixing and allowing the layers to separate, the ether layer is removed, dried, and concentrated to yield 0.68 mg of benzoic acid. What is the Kp value (ether/water) for this system?
separation of a three-component mixture by extraction, lab report help, the compounds are benzoic acid ,9-fluorene , and ethyl-4- aminobenzoate. I need help to write Discussion about this lab report a...
separation of a three-component mixture by extraction, lab report help, the compounds are benzoic acid ,9-fluorene , and ethyl-4- aminobenzoate. I need help to write Discussion about this lab report and I dont know what should I write.I got 25% recovary for benzoic acid ,32% for ethyl-4- aminobenzoate and 50 % recovary for 9-fluorene.( by the way I lost some product of benzoic acid). please help me full paper as you could for discussion and what is the source of...
A mixture of two compounds, A and B, was separated by extraction. After the compounds were...
A mixture of two compounds, A and B, was separated by extraction.
After the compounds were dried, their masses were found to be: 117
mg of compound A and 93 mg of compound B. Both compounds were
recrystallized and weighed again. After recrystallization, the mass
of compound A was 95 mg and the mass of compound B was 85 mg.
Calculate the percent recovery from recrystallization for both
compounds.
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)...
10. Using your answer to 6e: 6e: What percent of the mixture obtained in reaction 1...
10. Using your answer to 6e: 6e: What percent of the
mixture obtained in reaction 1 is the para isomer? para isomer :
37.9%
a) How many millimoles of the para product were
present in the isomeric mixture added in the first step of reaction
2? Please show your work.
b) In order to selectively acetylate the para isomer, equimolar
amounts of acetic anhydride and the para isomer must be present.
Using the millimoles you obtained as your answer to...
Using your answer to question 10 part a, calculate the theoretical amount (in mg) that was...
Using your answer to question 10 part a, calculate the
theoretical amount (in mg) that was expected for the
p-methyl acetanilide product. Be sure to show your
work.
10a: 37.9 x 17.5 / 100 = 6.6325mmol
Reaction 2: Reduction NO2 NH4HCO2 NH2 + NO2 Pd/C NO2 NH2 NH2 m-methylaniline p-methylaniline 0-methylaniline ortho meta para Procedure for Reaction 2: 1) The mixture of ortho, meta, and para isomers obtained from reaction 1 (2.4 g, 17.5 mmoles) was added to a 50...
a) Which products (shown above) from reaction 3 can react with HCl in an acid-base reaction?...
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?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
c) Why did we have to use hot ethanol for the
recrystallization?
d) Why did we have to cool the...
a) Which products (shown above) from reaction 3 can react with HCl in an acid-base reaction?...
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?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice...
A 577 mg of a mixture of fluorene and benzoic acid was weighed out and subjected to an extraction and recrystallization. After this purification was completed the product crystals were dried and analyzed. The purification procedure produced 247 mg of fluorene and 167 mg of benzoic acid. Calculate the percent composition of this mixture. Fluorene Benzoic Acid Number Number 0 0
A mixture of two compounds, A and B, was separated by extraction.
After the compounds were dried, their masses were found to be: 117
mg of compound A and 93 mg of compound B. Both compounds were
recrystallized and weighed again. After recrystallization, the mass
of compound A was 95 mg and the mass of compound B was 85 mg.
Calculate the percent recovery from recrystallization for both
compounds.
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)...
10. Using your answer to 6e: 6e: What percent of the
mixture obtained in reaction 1 is the para isomer? para isomer :
37.9%
a) How many millimoles of the para product were
present in the isomeric mixture added in the first step of reaction
2? Please show your work.
b) In order to selectively acetylate the para isomer, equimolar
amounts of acetic anhydride and the para isomer must be present.
Using the millimoles you obtained as your answer to...
Using your answer to question 10 part a, calculate the
theoretical amount (in mg) that was expected for the
p-methyl acetanilide product. Be sure to show your
work.
10a: 37.9 x 17.5 / 100 = 6.6325mmol
Reaction 2: Reduction NO2 NH4HCO2 NH2 + NO2 Pd/C NO2 NH2 NH2 m-methylaniline p-methylaniline 0-methylaniline ortho meta para Procedure for Reaction 2: 1) The mixture of ortho, meta, and para isomers obtained from reaction 1 (2.4 g, 17.5 mmoles) was added to a 50...
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?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
c) Why did we have to use hot ethanol for the
recrystallization?
d) Why did we have to cool the...
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?
b) Which phase (organic or aqueous) would the
p-methylacetanilide be found in?
In step 5 of reaction 3, the reaction mixture containing the products shown below in ethyl acetate is extracted twice...
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