O-2 Fractional Distillation Modified Procedure(1)
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O-2 Fractional Distillation Modified Procedure
For background and a more detailed explanation please review the experimental write-up
in “Laboratory Exercises for Organic Chemistry I and II”, Spring 2018, R. Gangi and R.
D. Rossi, pages 27-53, found in the content folder “Laboratory Notes”.
Download a free copy of LoggerPro from eLearning under the content folder “Important
Web Links” prior to analyzing the raw data for this experiment.
Imagine you set up the fractional distillation as illustrated in the video.
However instead of
using a thermometer a Labquest temperature probe was used in conjunction with a Labquest data
collection unit. Now you were given 5.0mL of an unknown mole percentage mixture of two
esters, ethyl acetate and butyl acetate (lookup the structures and physical properties of these two
materials).
Assume you placed 4.0mL the mixture into the distillation pot and subjected it to
fractional distillation.
Heating the mixture slowly, distilling at a pace that allowed you to record
a temperature reading for every 5.0 drops of distillate collected (see raw data file in this content
folder), you successfully collected three fractions of 10.0 drops each at the end of the distillation.
Analysis
You now subjected each of the three cuts, along with a control sample each of ethyl acetate and
butyl acetate, and the 1.0mL of the original unknown mole composition mixture of the esters to
gas chromatographic analysis as illustrated in the video using the temperature profile shown in
Table 1.
Start temperature
55°C
Hold time
1 min
Ramp rate
10°C/min
Final temperature
75°C
Hold time
2 min
Total length
5 min
Pressure
6.0 kPa
Sample Size
0.2μL
The raw GC data you collected is given in this content folder. You then proceeded to analyze the
chromatographs as described in the videos.
Related Questions
In the synthesis of Sudan-1, the following precursors were used:
Aniline – 0.2 mL
β-naphthol – 0.35 g
Experimental data
Weight of vial, g
13.1085
Weight of vial + recrystallized product, g
13.4714
Experimental melting point, °C
129-132
Given this data:
What is the theoretical yield?
What is the percent yield?
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Please show solutions and equations
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Time (min)
Concentration ()
0.5
6.01
1
11.78
1.5
17.6
2
23.51
2.5
29.58
3
35.31
3.5
39.73
4
44.5
4.5
48.18
5
50.05
5.5
52.72
6
54.01
6.5
55.06
7
55.65
7.5
56.39
8
56.74
8.5
57.49
9
58.03
9.5
58.61
10
58.69
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Related Questions
In the synthesis of Sudan-1, the following precursors were used:
Aniline – 0.2 mL
β-naphthol – 0.35 g
Experimental data
Weight of vial, g
13.1085
Weight of vial + recrystallized product, g
13.4714
Experimental melting point, °C
129-132
Given this data:
What is the theoretical yield?
What is the percent yield?
What is the purity of the dye based on experimental melting point (theoretical is 131-133 °C)
Please show solutions and equations
arrow_forward
Synthesis of Orange II dye.
During vacuum filtration, is it possible to use cold water for rinsing/collecting the Orange II dye? Clearly explain why or why not.
arrow_forward
Chemistry
Using FTIR to see structure change in quinine after exposing it to light for 2hr
seems like quinine degraded. Can it degrade by exposure to UV light for hours?
What source of errors could have happened? I know that maybe I used small concentration.
arrow_forward
Please type all of the parts to this question occordingly to the instructions.
Here is an example of a formal procedure based off of the experiment presented in Mohrig:Sodium hydroxide (4.6 g) was dissolved in water (25 mL). This solution was added to a 100 mL round bottom flask along with methyl salicylate (2.0 mL) and a stir bar. The mixture was heated at reflux for 15 min and then progressively cooled to 5 °C. The solution was acidified with 3M sulfuric acid (15-20 mL), and the resulting solid was collected by vacuum filtration. The crude salicylic acid was recrystallized from water to yield ???? g of final solid. The melting point and IR were taken to assess purity.
Calculate the molarity of the solution of sodium hydroxide that is used.a. M = b. If the original procedure is the base scale (100%), how far are we scaling down the reaction when using 0.75 mL of methyl salicylate? (Example: the original uses 2.0 mL, if we were to use 1.0 mL, we would be scaling the reaction down…
arrow_forward
Draw the synthesis setup for Ni(dppf)Cl2, make sure to include the round-bottom flask, reflux condenser, hotplate, and the connections to the vacuum and water-cooling systems.
Design an experiment remove separate Ca2+ and herbicide Atrazin (organochloride) from aqueous salt solution.
arrow_forward
Why is strict implementation of LQMS (Laboratory Quality Management System) or GLP is necessary ? What are the elements ?
arrow_forward
Fractioned Distillation Microscale
Looking at this set up, are there any potential problems with it? Please explain.
arrow_forward
Briefly, discuss reflux and why it is commonly used in organic chemistry.
arrow_forward
Explain two separation techniques how may be feasible for Benzene vs Phenol. One can be an industrial approach other can be a laboratory-scale method.
arrow_forward
The concentration of hydrolyzed nitrocefin at each time point for an experiment is given below.
Time (min)
Concentration ()
0.5
6.01
1
11.78
1.5
17.6
2
23.51
2.5
29.58
3
35.31
3.5
39.73
4
44.5
4.5
48.18
5
50.05
5.5
52.72
6
54.01
6.5
55.06
7
55.65
7.5
56.39
8
56.74
8.5
57.49
9
58.03
9.5
58.61
10
58.69
Make a graph that plots the concentration of hydrolyzed nitrocefin (in μM) against time (in seconds) using Excel, R, SPSS or other computable software. Where appropriate, include a trendline that shows the linear range on your graph. Include the equations for the trendlines and the R2 value on the graph. Your graph should also include a title and appropriate titles for the x- and y-axes, with units included where appropriate.
To determine the initial velocity of a possible insert in this experiment, you must determine what the linear range is in these data. Based on your graph, which time points represent a suitable linear range?
arrow_forward
Write TRUE if the underlined word/phrase makes the statement correct. Otherwise, write the correct WORD/PHRASE that will make the statement true. If there are two bold words/phrases in a number, write your answer for EACH of the bold words/phrases
1. 6-hydroxy-1-naphthoic acid is soluble in 5% NaOH and soluble in 5% NaHCO3.
2. The addition of excess charcoal would decrease the % recovery in the purification by recrystallization.
3. If the target compound is contaminated with impurity, the melting point will be higher than the theoretical value and the melting range is large.
arrow_forward
In an EAS Reaction the compounds 5.0g of acetanilide, 0.2g potassium bromate, 5ml acetic acid, 0.9 ml hydrobromic acid solution, and 5 ml saturated sodium bisulfite solution are used. Given these compound and obtaining a yield for the experiment at 6.3 grams which yields 5.3 grams after recrystallization and drying, Please find the theoretical yield and the percent yield?
arrow_forward
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SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
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Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
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ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
General, Organic, and Biological Chemistry
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ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
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ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,