Recrystalization Lab Report PDF

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Chemistry 212

WINTER 2015

RECRYSTALLIZATION
Solo Experiment 1 Individual Lab Report
(Save as pdf and submit, due by 12:00 NOON one week after experiment)

Last Name: OKeeffe


First Name: Laura
TA Name: Andrew Bruhac
Date Lab Performed: February 3, 2015
Date Lab Submitted: February 9, 2015
Group A, B, or C: B

Comments for Grading TA:


(Please indicate if you performed the lab on a day other than your regularly scheduled day and/
or with a TA other than your regular TA).

Page Limit: report must not exceed THREE pages (including this page)
LIMIT DOES NOT INCLUDE ANY GRAPHS, SPECTRA, OR REFERENCES
(Please see General Lab Report Guidelines for detailed descriptions of all other requirements)

DEDUCTIONS FOR HANDWRITTEN REPORT/STRUCTURES/GRAPHS


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Chemistry 212

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AND EXCEEDING PAGE LIMIT


LATE PENALTY IS 2 MARKS PER DAY LATE (NOT ACCEPTED AFTER 7 LATE
DAYS)
Solo Experiment 1: Recrystallization Report Sheet
Data: (10 marks)

MP: 169 172 C

Reactants:
Amount p-aminophenol used:
Amount acetic anhydride used:
(Show Calculations)

mass
mass

1.197g
1.296g

mol
mol

0.0110mol
0.0127mol

mol

0.0110mol

p-aminophenol:
n=m/M=(1.197g)/(109.13g/mol)=0.0110mol
Acetic anhydride:
d=m/V, m=dV=(1.08g/mL)(1.2mL)=1.296g
n=m/M=(1.296g)/(102.09g/mol)=0.0127mol
Product:
Theoretical Yield of Tylenol:
(Show Calculations)

mass

1.66g

Mole ratio between p-aminophenol and acetic anhydride is 1:1, therefore p-aminophenol is the
limiting reagent. The p-aminophenol:Tylenol is 1:1 as well, therefore nTylenol = 0.0110mol.
n=m/M, m=nM=(0.0110mol)(151.16g/mol)=1.66g
Table 1. Recrystallization Data
Crude Tylenol

Purified Tylenol

Yield (g)

1.197

0.26

Yield (%)

72

16

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Chemistry 212

Appearance
Melting Point

WINTER 2015
Yellow-brown discolouration, fine
powder

Off-white pink tint, larger crystals

146-150C

152-156C

Recovery (%)

22

Discussion Questions: (10 marks)


1. Given the following solubility test results, which would be the best recrystallization solvent
for Compound A? Why?
Ethanol: Cold soluble; Hot soluble
Water:
Cold insoluble; Hot soluble
Benzene: Cold insoluble; Hot - insoluble
Water, because when the solution is heated Compound A can be dissolved into the water
to make a super saturated solution. Then, as the solution is slowly cooled, Compound A will
crystalize due to its insolubility. These purified crystals can then be rinsed and collected.
2. How does recrystallization purify a solid?
An impure substance is dissolved into a hot solvent. The solvent must be carefully chosen
so that when hot, everything is dissolved, but when cool only the impurities are soluble while
the esired substance is insoluble. As the mixture cools slowly, selective crystalization of the
pure substance occurs, and the pure crystals can then be collected.
3. Briefly explain the significance of the melting-point results in regards to the purity of the
crude and recrystallized product.
Any impurities in a substance will reduce the its melting point, therefore the closer the
crude and purified Tylenols melting points to the accepted melting point of ~169C, the more
pure the product.
4. Suggest one chemical reason, specific to this experiment, why your percent recovery could be
less than 100%.
Any discolouration of the crude Tylenol is due to impurities, therefore once those are
removed, any mass associated with them is removed as well, making the percent recovery less
than 100%. My crude product had a yellow-brown discolouration, meaning impurities were
present, contributing to the mass. Once they were removed the mass would decrease and
make the percent recover less than 100%.

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