Download Chemistry 209 - Experiment 3, Fall 2002

EXPERIMENT 3
Properties of Alcohols, Phenols, and Amines - Solubility and Reactions
Materials Needed
isopropyl alcohol, tert-butyl alcohol, 1-octanol, 2-naphthol, dodecylamine, glycerol
18 small test tubes
distilled water, hexane, 3 M HCl(aq), 3 M NaOH(aq), conc. H2SO4(aq), CrO3/H2SO4 solution, acetone
Additional Reading Assignment
McMurry, chap 14.1-14.7, 15.1-15.2, 15.4-15.5
Introduction
In this lab we will again examine how the structure of a molecule determines the properties of the
compound. In particular, you will explore some of the properties of a small group of oxygen and nitrogen-containing
compounds. The reactivity of each compound with a series of reactants (3 M HCl(aq), 3 M NaOH(aq), conc.
H2SO4(aq), CrO3/H2SO4 solution) will be determined. In addition, you will look up literature values for the melting
point and boiling point of all of the compounds tested.
As in the previous experiment, you should make a note of as many characteristics of the substances to be
tested as possible. Always note the color and physical form of each compound you work with in the lab. As you
perform the different tests, try to observe and note any subtle differences between the behavior of different
compounds. Such things as color changes, warming of the solution ("heat evolution"), bubbling ("gas evolution"),
should all be carefully noted.
Background
Water Solubility Test. The general rule for solubility is "like dissolves like". Hence water, a very polar
solvent, dissolves only the most polar organic compounds, for example, salts of organic acids, salts of organic bases,
lower molecular weight alcohols and amines (e.g., ethanol, methylamine), and polyhydroxy compounds (e.g. sugars).
Non-polar compounds do not dissolve in water.
Hexane Solubility Test. Only non-polar compounds will dissolve in this very non-polar alkane solvent.
Reactivity with 3 M HCl(aq). This acid reacts with basic organic compounds such as amines. Signs of
reaction include heat evolution and dissolution. (If a compound does not dissolve in water but does dissolve in
HCl(aq) then it must be reacting with the HCl.)
Reactivity with 3 M NaOH(aq). This base reacts with acidic organic compounds such as carboxylic acids
and phenols. Signs of reaction include heat evolution and dissolution. (If a compound does not dissolve in water but
does dissolve in NaOH(aq) then it must be reacting with the NaOH.)
Reactivity with concentrated sulfuric acid. Concentrated sulfuric acid is a very strong acid that is capable
of protonating compounds that have available electron pairs. The unshared pairs of electrons in oxygen and nitrogen
containing compounds are readily protonated as are the extra electrons in a double or triple bond. (See eq 1-2). Signs
of reaction include strong evolution of heat or gas fumes, or a color change.
Reactivity with CrO3/H2SO4 solution. (See pp 375-376 in McMurry). The chromium(VI) is an oxidizing
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agent that can oxidize alcohols. A reaction is indicated by a change in color from orange to green:
Cr6+
orange
+
3e-
Cr3+
green
LABORATORY PROCEDURE
SAFETY PRECAUTIONS
- WEAR YOUR SAFETY GOGGLES AT ALL TIMES.
- IF YOU SPILL A SOLUTION ON YOUR SKIN, BE SURE TO FLUSH THE AREA PROMPTLY WITH LOTS
OF WATER.
- TAKE SPECIAL CARE WITH CONC. H2SO4 AND WITH THE CrO3 SOLUTION. IF YOU GET ANY
ON YOUR SKIN OR CLOTHING, RINSE IT WITH WATER IMMEDIATELY. DOING SO WILL AVOID
SERIOUS INJURY.
- IF YOU ACCIDENTALLY SPILL CONC. H2SO4 OR CrO3 SOLUTION ANYWHERE IN THE LAB NOTIFY
THE INSTRUCTOR OR T.A. IMMEDIATELY.
- CARRY OUT THE HEXANE SOLUBILITY, H2SO4 AND CrO3 TESTS WHILE WORKING IN A
FUMEHOOD.
- WEAR GLOVES WHEN CARRYING OUT THE SOLUBILITY AND REACTIVITY TESTS. SOME OF THE
SOLUTION MAY LEAK OUT OF THE TUBE WHEN IT IS BEING SHAKEN SO YOUR HANDS NEED TO
BE PROTECTED.
General procedure for solubility tests
Place approx. 0.2 mL (4-5 drops) of the liquid or approx. 0.1 g (1 small spatula tip) of the solid to be tested,
in a test tube and add a total of approx. 3 mL of the solvent (either distilled water or hexane) in several portions.
Cover the tube with a cork or rubber sleeve stopper and shake it vigorously so as to mix the contents thoroughly after
each addition of solvent. If the substance dissolves completely, record it as soluble. Continue shaking for at least
five minutes if the substance does not dissolve at first in order to make sure you have allowed adequate time for
dissolution to take place.
Sometimes, especially for liquids, it is difficult to decide whether or not a substance has dissolved. After
thorough mixing, allow the sample to stand motionless for 2 minutes. If the original two liquid layers reappear, you
should record the substance as insoluble. Likewise, if the solution becomes cloudy and does not clear upon standing,
you can consider the substance insoluble. When testing liquid samples, be sure to look carefully for a layer of
undissolved liquid, which may be either lying on top or at the very bottom of the test tube.
Solubility in H2O. Test all six compounds using distilled water as the solvent. (Use the general procedure
given above.) For insoluble liquids observe whether the substance is more or less dense than water.
Solubility in hexane. Test the solubility of all six compounds using hexane as the solvent, again using the
general procedure given above. Discard the resulting solutions in the bottle labeled "waste hexane" in the
hood.
Reactivity with 3 M NaOH(aq). Use the general procedure for solubility tests to test only the compounds that did
not dissolve in water. Use 3 M NaOH(aq) as the solvent. Watch carefully for any sign of reaction as
discussed in the background.
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Reactivity with 3 M HCl(aq). Use the general procedure for solubility tests to test only the compounds that did
not dissolve in water. Use 3 M HCl(aq) as the solvent. Watch carefully for any sign of reaction as discussed
in the background.
Reactivity with Concentrated H2SO4
Only test the compounds that showed no reaction with 3 M HCl. (If a compound reacts with 3 M HCl. it
may be safely assumed that it would also react with concentrated H2SO4.) Test the same amounts of all four
compounds that you used in the other tests. Use a dry test tube and carefully add only 5-6 drops (not 3 mL as in the
other tests) of concentrated H2SO4. Observe the results carefully and note exactly what happens on the data table. If
the substance reacts, heat will be evolved, and often a dark color will appear.
Reactivity with CrO3/H2SO4 solution.
Test the three alcohols only. Do not test the naphthol, the amine, or the glycerol. Place 1-2 drops of the
alcohol in a test tube and add a total of approx. 3 mL of acetone. The alcohol should easily dissolve. Now add 5-6
drops of the CrO3/H2SO4 solution. Make sure to observe carefully the color of the CrO 3/H2SO4 solution before
adding it and the color of the test solution after adding the CrO3/H2SO4.
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PRE-LABORATORY QUESTIONS
EXPERIMENT 3
Properties of Alcohols, Phenols, and Amines - Solubility and Reactions
Name ____________________________________________________________________ Date ____________
1.
Give the structures of the compounds being tested in this lab: isopropyl alcohol, tert-butyl alcohol, 1-octanol, 2naphthol, dodecylamine, and glycerol. Most of these you will be able to find in the McMurry textbook or be able
to figure out from nomenclature rules. A few you may have look elsewhere (i.e., the Internet or an organic
chemistry textbook or other chemistry reference book.)
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IN-LAB OBSERVATIONS/DATA
EXPERIMENT 3 - Properties of Alcohols, Phenols, and Amines
Names ____________________________________________________________________Date ____________
isopropyl alcohol:
general observations ____________________________________________________________________
solubility in water ____________________________ density (if insoluble)_________________________
solubility in hexane _____________________________________________________________________
reactivity with 3 M NaOH ________________________________________________________________
reactivity with 3 M HCl __________________________________________________________________
reactivity with conc H2SO4 ________________________________________________________________
reactivity with CrO3/H2SO4________________________________________________________________
tert-butyl alcohol:
general observations ____________________________________________________________________
solubility in water ____________________________ density (if insoluble)_________________________
solubility in hexane _____________________________________________________________________
reactivity with 3 M NaOH ________________________________________________________________
reactivity with 3 M HCl __________________________________________________________________
reactivity with conc H2SO4 ________________________________________________________________
reactivity with CrO3/H2SO4________________________________________________________________
1-octanol:
general observations ____________________________________________________________________
solubility in water ____________________________ density (if insoluble)_________________________
solubility in hexane _____________________________________________________________________
reactivity with 3 M NaOH ________________________________________________________________
reactivity with 3 M HCl __________________________________________________________________
reactivity with conc H2SO4 ________________________________________________________________
reactivity with CrO3/H2SO4________________________________________________________________
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EXPT #3
IN-LAB OBSERVATIONS/DATA (continued)
2-naphthol:
general observations ____________________________________________________________________
solubility in water ____________________________ density (if insoluble)_________________________
solubility in hexane _____________________________________________________________________
reactivity with 3 M NaOH ________________________________________________________________
reactivity with 3 M HCl __________________________________________________________________
reactivity with conc H2SO4 ________________________________________________________________
dodecylamine:
general observations ____________________________________________________________________
solubility in water ____________________________ density (if insoluble)_________________________
solubility in hexane _____________________________________________________________________
reactivity with 3 M NaOH ________________________________________________________________
reactivity with 3 M HCl __________________________________________________________________
reactivity with conc H2SO4 ________________________________________________________________
glycerol:
general observations ____________________________________________________________________
solubility in water ____________________________ density (if insoluble)_________________________
solubility in hexane _____________________________________________________________________
reactivity with 3 M NaOH ________________________________________________________________
reactivity with 3 M HCl __________________________________________________________________
reactivity with conc H2SO4 ________________________________________________________________
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REPORT - EXPERIMENT 3
Results Table
EXPERIMENT 3 - Properties of Alcohols, Phenols, and Amines
Name _____________________________________________________________________________________________________________Date __________
Compound
Name and
Structure
isopropyl
alcohol
Appearance
Results of Solubility/Reactivity Tests
H2O
density
hexane
3 M NaOH
3 M HCl
conc H2SO4
lit bp (C)
CrO3/ H2SO4
tert-butyl
alcohol
1-octanol
2-naphthol
na
dodecylamine
na
glycerol
na
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lit mp (C)
QUESTIONS
1.
Only one of the six compounds tested should have shown any reaction in the NaOH test. Which one is it?
Explain. Write an equation for the reaction.
2.
Only one of the six compounds tested should have shown any reaction in the HCl test. Which one is it? Explain.
Write an equation for the reaction.
3.
Two of the three alcohols tested should have reacted with CrO3/ H2SO4. (a) Show equations for these reactions.
(b) Explain why the other alcohol did not react with CrO3/ H2SO4
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