Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
Experiment A. Introduction to the Organic Laboratory and
Characterization Techniques
______________________________________________________
1. EXPERIMENTAL OBJECTIVES:
a. To identify the safety features and physical layout of the organic laboratory.
b. To locate and operate instruments and equipment in the laboratory.
c. To recrystallize a pure sample of either benzoic acid (compound 1) or naphthalene
(compound 2).
O
OH
1
2
d. Characterize benzoic acid (1), naphthalene (2), and a mixture of these two by melting
point analysis.
e. To conduct thin layer chromatography and analysis of common household products
(Anacin, Excedrin, Tylenol, aspirin, caffeine).
2. SPECIAL INSTRUCTIONS:
a. You will not turn in your lab notebook pages for grade. You will only turn in the “fill
in the blank” style report for grade at the end of the second three-hour period. You should,
however, complete your lab notebook according to procedures as described in your SICOC to
familiarize yourself with laboratory notebook requirements. For notebook purposes, this is your
practice lab.
b. Efficiently inventory your bench drawers throughout the lab period. Do not spend an
inordinate amount of time on the inventory. Become familiar with the equipment, note
discrepancies and replenish as appropriate.
c. Choke point for lab is melting point determination.
d. Chemicals and solvents Chemical Abstract Service [CAS]:
(1) Benzoic Acid, [65-85-0]
(2) naphthalene, [91-20-3]
(3) hexane, [110-54-3]
(4) methanol, [67-56-1]
(5) acetone, [67-64-1]
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
3. PROCEDURES:
Perform the following tasks. Remember, you must multitask to be successful.
1. Inventory and Orientation. Inventory the contents of your lab bench drawers. If you are
missing anything, attempt to re-stock your drawers from the various equipment supply points. If
an item is unavailable, bring it to the attention of your instructor. Inventory sheet is attached.
Conduct an inspection of the laboratory facilities to identify the safety items, equipment,
function, and apparatus locations, and waste disposal receptacles. Record on the attached page
and laboratory map; attach the map permanently into your laboratory notebook and identify its
location in the Table of Contents.
2. Thin-Layer Chromatography. Using the five compounds, prepare each sample in a 3-mL
disposable test tubes using about 1 ml of the prepared solvent mixture (1:1 hexane: acetone) as
the dissolving solvent and a smallest quantity of solid on your spatula tip.
a. Prepare a TLC developing chamber (G&M, Fig 6.3, p. 177), using the prepared solvent
mixture (1:1 hexane:acetone) as the developing solvent.
b. Prepare two TLC plates (G&M, Fig 6.2, p. 177):
(1) Prepare a plate with caffeine, aspirin, and acetaminophen; prepare a second
plate with Unknowns A and B.
(2) Label your TLC plates per G&M. Use only pencil. Draw a sketch of your
plates in your lab notebook.
(3) Spot each of the samples on the TLC plate, ensuring that the spot is above the
solvent level in the developing chamber.
c. Elute the plate in the developing chamber. Stop the process before the solvent front
reaches the top of the TLC plate. Remove the plate and immediately mark the solvent front with
pencil.
d. Observe the elution by visualizing the TLC spots under UV light, tracing around the
spots observed and marking the center mass of each spot.
e. Calculate the Rf values (G&M, p. 179) of each compound in the samples by
determining
the ratio of distance of sample travel/distance of solvent travel in the space provided on your lab
report.
f. Include the fully labeled and analyzed TLC plates with your lab report.
3. Capillary Melting Point Analysis. Prepare three capillary tubes (G&M, Fig 2.16, p. 39 and
Fig 2.19, p. 40) for melting point analysis of pure benzoic acid, pure naphthalene, and a 80%20% benzoic acid/naphthalene mixture of the two (already prepared for you). Determine the
melting point range for each sample, record the data in your notebook, and enter it in your lab
report.
4. Craig Tube Recrystallization; Centrifuge Operation. Ensure the hotplate sandbath is
heated to at least 80 °C for this procedure.
a. Record the exact mass of either approximately 0.075 g of naphthalene and place it into
a Craig tube (G&M, Fig 2.47, p. 66). To the naphthalene, add about 1 mL methanol.
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
b. Heat "gently" on the sandbath until the solid dissolves. It is best to tap the Craig tube
to aid dissolution rather than stirring, as stirring with the spatula results in transfer losses. If you
must stir, use the microspatua. (Note: heating "gently" is an art form that means use your
calibrated senses to heat the tube enough to get the contents just warm enough to aid solvation
but not too hot to cause boiling. Too much solvent inhibits recrystallization, so selecting the
solvent and its volume is also an art form.)
c. Upon dissolution, remove the Craig tube from the sandbath and set it in a small beaker
to keep it upright while cooling in air.
d. After the reaching room temperature, cool the tube in an ice bath for a few minutes to
enable crystal growth.
e. After crystals have formed, insert the glass plunger with wire into the Craig tube to
form the "Craig tube assembly," (G&M, Fig 2.47, p. 66). Now remove the solvent by inverting
the Craig tube assembly into a centrifuge tube (G&M, Fig 2.55, p. 71). Place the inverted Craig
tube assembly into the centrifuge, balance the centrifuge, and then spin the mother liquors from
the crystals to the bottom of the centrifuge tube.
f. After spinning, carefully remove the centrifuge tube with the Craig tube assembly, pull
the wire to remove the Craig tube from the centrifuge tube, then disassemble the Craig tube
assembly and carefully collect the crystals from the plunger and the Craig tube. Determine the
mass of the recovered product and record it on the lab report.
5. Disposal of Chemical and Solid Waste. Discard pipets and weighing boats in trash
receptacles; discard any glass in the glass waste box. Solvents go in the solvent bottles in the
hood.
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
Inventory Sheet
Top Drawer:
□1 sand bath (crystallizing dish containing sand)
□1 aluminum heating block
□4 round bottom flasks (1 with threaded compression cap, septum, and o-ring)
□4 conical vials (2x3 mL and 2x5 mL, all with threaded compression caps, septa, and o-rings)
□1 conical vial cap
□1 centrifuge tube cap
□3 types of stir bars (1 spin-vane and 2 bars)
□1 Hirsch funnel with neoprene adapter
□1 filter flask
□4 beakers (2x10 mL and 2x30 mL)
□3 Erlenmeyer flasks (2x5 mL and 1x 25 mL)
□1 permanent marker
□2 spatula
□1 glass rod with rubber policeman
□1 pair of tweezers
□1 rubber adapter
□1 long thermometer
□1 microscale lab kit (blue box), containing:
□4 conical vials (2x1 mL, 1x3 mL and 1x5 mL, all with threaded compression caps,
septa, and o-rings)
□2 V bottom vials (both with threaded compression caps, septa, and o-rings)
□1 Hickman-Hinkel still head
□1 condenser
□1 syringe
□1 air condenser
□1 Craig tube for recrystallization
□1 plunger for Craig tube
□1 drying tube
□1 Claisen head
□1 round bottom flask (with threaded compression cap, septum, and o-ring)
□1 thermometer adapter
□2 collection tubes
□1 collection tube adapter (metallic)
2nd Drawer:
□2 beakers (1x250 mL, 1x100 mL)
□1 separatory funnel
□3 funnels (2 glass, 1 plastic)
□1 wide-mouth jar for TLC development
□1 graduated cylinder
□1 ruler
□1 brush
□1 evaporating dish
□1 watch glass
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
Supplies of:
□red litmus paper
□blue litmus paper
□micropipettes
□boiling stones
□filter paper (5.5 cm and 1 cm)
□melting point tubes
□matches
□pHydrion paper
□TLC plates
Third drawer:
□1 test tube clamp
□1 pair forceps
□1 towel
□1 test tube rack
□1 hose clamp
□1 wire gauze
□1 fiberglass hot mat
□1 hose clamp
Bottom drawer:
□Assortment of hoses
□5 clamps (all different types)
□1 ring
□1 cork ring
□1 microburner
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
Orientation to the Organic Laboratory
Identify and record the location of the items listed in the laboratory. Keep this page for
successive lab periods.
Nearest fire extinguisher/Spill Control Center
_____________________
Nearest eyewash station/shower
_____________________
Instructor’s bench
_____________________
Ms. Wade’s office
_____________________
Nearest telephone; phone number
_____________________
Material Safety Data Sheet (MSDS) folder
_____________________
CRC, spectra, and reference books
_____________________
Solid, liquid organic waste disposal bottles
_____________________
Broken glass/glass disposal box
_____________________
Chemical dispensing hoods
_____________________
Sandbath equipped drying hood
_____________________
Icemaker
_____________________
Drying oven
_____________________
UV lamps for visualization
_____________________
Centrifuges
_____________________
Melting temperature apparatus
_____________________
Heating lamps
_____________________
Balances
_____________________
Gas Chromatography (GC) instruments
_____________________
Infrared (IR) Spectroscopy instruments
_____________________
Student sample temporary storage cabinet
_____________________
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
A Building, Room 1290 Schematic: Organic Chemistry Laboratory Layout
Door
Prep Room
Door
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
Experiment A Report
Name:___________________
Date: ___________________
(12) 1. Thin Layer Chromatography
a. (True/False) For a given sample, a single TLC spot is an absolute indication of sample
purity. Explain.
b. If a solvent such as ethanol (instead of a solvent mixture such as acetone/hexane) were
used to elute the samples on the TLC plate, would you expect the Rf values to be greater or less
than those you recorded? Explain your answer.
c. Show your calculations for the Rf values of each of the 5 compounds below.
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
d. Unknown A and Unknown B are common over the counter (OTC) analgesics Anacin
and Excedrin. Which unknown is Anacin and which is Excedrin? How do you
know?
(15) 2. Capillary Melting Point Analysis
a. Complete the table below.
Compound
Lit m.p.
(oC)
Heating rate
(deg/min)
Starts
Melting
Stops
Melting
T
T
(Tstop-Tstart)  2oC ?
benzoic acid
naphthalene
80%-20% mixture
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
b. How close was the range to the expected melting point values for the compounds?
c. Were these compounds pure? Explain.
d. What impact did the presence of the other compound have on the melting point range
of the mixture?
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
e. Is the melting point of the mixture exactly between the melting point temperatures of
the pure samples? Consider the breadth of range and relation to literature m.p. Why or why not?
Discuss your melting point analysis in the framework of colligative properties you learned in
general chemistry. In addition, you may discuss instrument calibration in your explanation.
(12) 3. Craig Tube Recrystallization
a. Set up and calculate % recovery for your recrystallized product.
b. Discuss your percent recovery in the framework of less than, greater than, or equal to
100% recovery.
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Organic Chemistry I Lab
CHEM 2211L (Fall 2008)
School of Science & Technology
Georgia Gwinnett College
c. Would a solvent such as hexane dissolve benzoic acid as effectively as water? Why or
why not?
d. Compare color of the solvent before adding the solid with color of solvent after
centrifuging. Explain.
e. What differences, if any, did you observe in the physical appearance of your
recrystallized compound and the initial starting material? Explain.
(1) 4. Sand Bath Calibration. What do you conclude about your sand bath as a heating source?
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