6th sub
.pdf
keyboard_arrow_up
School
Wayne State University *
*We aren’t endorsed by this school
Course
2230 #
Subject
Chemistry
Date
Apr 3, 2024
Type
Pages
1
Uploaded by DoctorEchidnaPerson2063
e S tm— Report Sheol: TLC and Column Chromatography e l‘ Name; i S0 sectiont o Dater N Initial TLC Analysis Record your TLC results below, 1. Draw the starting line, solvent front line and ferrocene and acetyl ferrocene spots on each of the three TLC plates drawn for you below, 2. Calculate R for both spots on each of the three TLC (show calculations at bottom of page). 3. Label the identity of both spots (2 spots per TLC) on each of the three TLC below. 100% petroleum ether 9:1 petroleum ether:dicthyl ether 1:1 petroleum ether:dicthyl ether 6| 5-2em | Y9 em — - el o d-6cm o Y.levn o | 3-6em o— 1 A1 14\ O— |1-Cem o | ] 0B em ] RO a 1| (q: & ! Report Figure CH.1 N Calculations 1. Which solvent did you run the TLC with the mixture and two pure compounds? (Petroleum ether ~ OR 9:1 ethyl diethyl ether OR 1:1 pet ether/diethyl ether) 2. Draw the starting line, solvent front line and three sets of spots (pure ferrocene, pure acetylferrocene and mixture of ferrocene and acetyl ferrocene) on the TLC plates drawn for you below. 3. Calculate Ry for all spots on the TLC (show calculations at bottom of page). 4. Label the identity of all spots on the TLC below. Laboratory Manual Prepared by Catalyst Education, LLC for Wayne State University CH. Department of Chemlstry. ' Scanned with CamScanner
Discover more documents: Sign up today!
Unlock a world of knowledge! Explore tailored content for a richer learning experience. Here's what you'll get:
- Access to all documents
- Unlimited textbook solutions
- 24/7 expert homework help
Related Questions
The TLC plate is show below
with pet ether-acetone mixture
(3:1) as the mobile phase.
Which spot is the most
nonpolar? *
O A
O E
1O D
MADE IN ENGLAND
L wɔ 0
E.
arrow_forward
You spotted a mixture of three compounds, labeled A-C, on a silica plate. The resulting thin layer chromatography (TLC) plate with a mobile solvent mixture of 95 % hexanes and 5 % ethyl acetate is shown below.
Which of the spots traveled the furthest up the TLC plate corresponding to spot 3?
arrow_forward
How do you calculate the retention factor (Rf) for each spot ?
Distance traveled by spot O 5.5cm
Distance traveled by spot Y 4.0cm
Distance traveled by spot G 3.0cm
Distance traveled by solvent front 6.0cm
arrow_forward
6. Say you are trying to separate two compounds by column chromatography. You run a column
and collect the eluent in five fractions. You analyze each fraction by TLC on the same plate
(shown below). Based on the TLC plate, how effective was your separation?
-------1---
1 2 3 4 5
arrow_forward
Which of the following statements regarding thin layer chromatography are correct?
O a. The larger a Rf of a compound, the larger distance it travels on TLC plate
O b. When comparing two different compounds, the compound with the larger Rf is more polar
O c. Larger Rf means compounds interact weaker with polar surface on the TLC
O d. Polar compounds interact more strongly with polar surface of TLC and move faster
e. a and b
f. a and c
arrow_forward
a. Say you are trying to separate two compounds by column chromatography. You run a column and
collect the eluent in five fractions. You analyze each fraction by TLC on the same plate (shown below).
Based on the TLC plate, how effective was your separation? Consider the purity of each fraction.
- - - - - - - - ----|
1 2 3 4 5
arrow_forward
please answer a,b,c,d
arrow_forward
See image below
arrow_forward
i need to caluclate a rf value for the tlc plate and i really need help with showing the steps please!
Reduction of 4-Nitrobenzaldehyde to 4-Nitrobenzyl Alcohol and Thin Layer Chromatography
arrow_forward
A student used thin layer chromatography to confirm whether he could successfully separate two compounds. Here is the TLC plate he obtained after 30 min. Stationary phase was silica gel and mobile phase was 95 % ethyl acetate and 5 % Hexane mixture.
arrow_forward
Qno1: why there is a need of chromatography and chromatography thecniqs. B) when and where we should use normal and reverse phase chromatography
arrow_forward
Internal standard. A mixture containing 12.8 mM analyte (X) and 44.4 mM standard (S) gave chromatographic peak areas of 306 for X and 511 for S. A second solution containing an unknown quantity of X plus 55.5 mM S had peak areas of 251 for X and 563 for S. Find [X] in the second solution.
arrow_forward
calculate Rfs for each spot on your chromatogram
arrow_forward
(please answer all questions)
5-30. When marking the sample line on a TLC plate, why is it inadvisable to use a ball-point pen?
5-31. A series of dyes is separated by TLC. The data are given below. Calculate the Rf value for each dye.
5-32. Why is it important not to let the level of the elution solvent in a packed chromatographic column drop below thetop of the solid-phase adsorbent?
5-33. What are some advantages of using column chromatography to purify reaction products in the microscalelaboratory?
5-34. Discuss the similarities and dissimilarities of TLC, paper, and column chromatography.
5-35. Discuss the similarities and dissimilarities of HPLC and gas chromatography.
5-36. (a) What are the main advantages of using flash chromatography?(b) How can TLC be used in connection with flash chromatography?
5-37. Using the information presented on the right, please identify and explainwhich spot has an Rf value of 0.5.
arrow_forward
Match column A with Column B. Everything is all about column Chromatography
v Least polar molecules
A. Eluate
v most polar molecule
B. eluted first
the mobile phase
C. silica
v stationary phase
D. eluted last
molecules eluted together with the solvent
E. Eluent
v to removelextract/wash
F. Elute
arrow_forward
30. Can you explain explain liquid chromatographic separation....
And how to solve problems akin to this?
arrow_forward
How can we answer
arrow_forward
Study the chromatograph (below) of a mixture of Compounds A and B, run on the GCs in the teaching labs at CU Boulder. Compound A has the shorter retention time.
You suspect that compound B is octane. What can you do to provide supporting evidence for this hypothesis?
arrow_forward
So I completing a lab report and one of the sections is on TLC analysis. In the experiment, the TLC plate was submerged in toluene ethylacetate and had spots of cinnamon leaf oil, cinnamon aldehyde, and cinnamon bark oil. 9 spots total were seen under the UV light, but different spots appeared following a vanillin stain. Why is this so and what does this mean?
arrow_forward
1) Aspirin
2) Acetaminophen
3) Ibuprofen
4) Caffeine
arrow_forward
Why Rf value is important in Chromatography? Please shortly answer at your own words. Answer should be the point (specific 4-5 lines).
arrow_forward
I just need letter h please
arrow_forward
Record your absorbance data for the YELLOW and RED dyes below. Calculate the dye concentration in mM for each cuvette using M1V2 = M2v2 . Remember the concentration of stock solutions (100^ % dye) is 0.020 mM(mM= millimolar =mm /L).
Data for YELLOW: peak absorbance used on spectrophotometer =420nm
Cuvette 1 - 100% dye = 0.680 absorption
Cuvette 2 - 75% dye = 0.510 absorption
Cuvette 3 - 50% dye = 0.340 absorption
Cuvette 4 - 25% dye = 0.170 absorption
Data for RED - peak absorption used on spectrophotometer = 500nm
Cuvette 1 - 100% dye: 0.621 absorption
Cuvette 2 - 75%: 0.466 absorption
Cuvette 3 - 50% dye: 0.311 absorption
Cuvette 4 - 25% dye: 0.1555 absorption
arrow_forward
Answer sections C, D and E in the same answer book.
Section D (Chromatography)
Question 8
The following data were obtained for the analysis of a mixture of compounds (A-D) by
HPLC:
Peak
Retention time (min) | Width of peak base (min)
non-retained
2.1
A
6.4
10.51
B
11.3
1.03
C
13.1
1.25
D
21.6
1.62
a) Using peak C. calculate the number of plates (N) in this column.
b) For peak D, calculate the capacity factor (k').
c) For peak B and C, calculate the resolution (R).
arrow_forward
How can I calculate the concentration from a GC/MS chromatogram which is having retention time and peak area only?
arrow_forward
A solution was prepared by mixing 12.49 mg of B plus 10.00 mL of unknown containing A and just diluting to 25.00 mL. Peak areas of 5.97 and 6.38 were observed for A and B, respectively. Find the concentration of A (mg/L) in the unknown.
arrow_forward
HPLC VFA analysis - why do I get so different peaks for very similar samples?
arrow_forward
Please find the Rf values of each drug and the name of the unknown sample!
arrow_forward
When the use of 2D Thin layer Chromatography is better than normal TLC? Please shortly answer at your own words. Answer should be to the point (specific 4-5 lines).
arrow_forward
3 Compare:
a) Capillary Electrophoresis with GC and HPLC.
b) Separation Versus Preconcentration.
arrow_forward
See image below
arrow_forward
Q1) The chromatogram below show a separation of a mixture of 2 components injected in a 25-1cm column at a flow rate of 0.4 mlmin.Answer the following questions :a. Find the times that components A and B spend in the stationary phase.b. Find the retention times for A and B.c. Determine the retention factors for the two components.d. Find the full widths of each peak and the full width at half maximum values.e. Find the resolution of the two peaks.f. Find the average number of plates for the column.g. Find the average plate height.h. What column length would be needed to achieve a resolution of 1.75?i. What time would be required to achieve the resolution in part h.j. Assume that the column length is fixed at 25 cm and the packing material is fixed. Whatmeasurescould you take to increase the resolution to achieve baseline separation?k. Are there any measures you could use to achieve a better separation in a shorter time withthe samecolumn as in part j?
arrow_forward
Olivia developed a new dye called Dye C. It was analyzed against other dyes using paper
chromatography. A solution of 1:1 ethyl acetate:hexane was used as the eluent. The resulting
chromatogram is shown below.
2 3 4 5 6
0 cm 1
A
B C
D E
F
G
a.
Determine the retention factor (Rf) values of each spot on dye C. Report your answer in 2
decimal places.
b. What other dye/s are present in dye C?
c. Which dye contains the least number of pigments?
arrow_forward
Can you TYPE the definitions of the all of words please
Chromatography
TLC
Stationary phase
Mobile phase
Elute
Eluent
Rf Value
Elution chamber
TLC “spotter”
arrow_forward
1) Study the chromatograph (below) of a mixture of Compounds A and B, run on the GCs in the
teaching labs at CU Boulder. Compound A has the shorter retention time.
STAAT
61
1.11
227
RT
TYPE
AREA
XXXX
XXXX
XXXX
AREAS
0.009
55874
44.117
ARIHT
0.61
XX
XX
XX
1.11
2.27
XX
XX
XX
TOTAL AREA=XX
MUL FACTOR=XX
1. What is the retention time of compound A? Compound B?
2. Which compound is present in a larger amount?
3. Which compound has the lower boiling point?
4. What would happen to the retention times of compounds A and B if the column temperature were
raised?
5. You suspect that compound B is octane. What can you do to provide supporting evidence for this
hypothesis?
arrow_forward
How can you use ion exchange Chromatography to de-ionize water? Please shortly answer at your own words. Answer should be to the point (specific 4-5 lines).
arrow_forward
SEE MORE QUESTIONS
Recommended textbooks for you
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT
Related Questions
- The TLC plate is show below with pet ether-acetone mixture (3:1) as the mobile phase. Which spot is the most nonpolar? * O A O E 1O D MADE IN ENGLAND L wɔ 0 E.arrow_forwardYou spotted a mixture of three compounds, labeled A-C, on a silica plate. The resulting thin layer chromatography (TLC) plate with a mobile solvent mixture of 95 % hexanes and 5 % ethyl acetate is shown below. Which of the spots traveled the furthest up the TLC plate corresponding to spot 3?arrow_forwardHow do you calculate the retention factor (Rf) for each spot ? Distance traveled by spot O 5.5cm Distance traveled by spot Y 4.0cm Distance traveled by spot G 3.0cm Distance traveled by solvent front 6.0cmarrow_forward
- 6. Say you are trying to separate two compounds by column chromatography. You run a column and collect the eluent in five fractions. You analyze each fraction by TLC on the same plate (shown below). Based on the TLC plate, how effective was your separation? -------1--- 1 2 3 4 5arrow_forwardWhich of the following statements regarding thin layer chromatography are correct? O a. The larger a Rf of a compound, the larger distance it travels on TLC plate O b. When comparing two different compounds, the compound with the larger Rf is more polar O c. Larger Rf means compounds interact weaker with polar surface on the TLC O d. Polar compounds interact more strongly with polar surface of TLC and move faster e. a and b f. a and carrow_forwarda. Say you are trying to separate two compounds by column chromatography. You run a column and collect the eluent in five fractions. You analyze each fraction by TLC on the same plate (shown below). Based on the TLC plate, how effective was your separation? Consider the purity of each fraction. - - - - - - - - ----| 1 2 3 4 5arrow_forward
- A student used thin layer chromatography to confirm whether he could successfully separate two compounds. Here is the TLC plate he obtained after 30 min. Stationary phase was silica gel and mobile phase was 95 % ethyl acetate and 5 % Hexane mixture.arrow_forwardQno1: why there is a need of chromatography and chromatography thecniqs. B) when and where we should use normal and reverse phase chromatographyarrow_forwardInternal standard. A mixture containing 12.8 mM analyte (X) and 44.4 mM standard (S) gave chromatographic peak areas of 306 for X and 511 for S. A second solution containing an unknown quantity of X plus 55.5 mM S had peak areas of 251 for X and 563 for S. Find [X] in the second solution.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- EBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENT
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT