Question
can you please answer all

1. When you run a TLC of the reaction in ethyl acetate : hexanes 1:1, the plate below is produced. Give a solvent system that

4. After running column chromatographie separation, you have a series of test tubes Describe how you know which tubes to comb
0 0
Add a comment Improve this question Transcribed image text
Answer #1

1. A) From given system of ethyl :hexane 1:1
That is, 50% system is too much polar for given compounds .To get better separation TLC should be run in less polar system so that Rf of the compound will be less and separation will be more .The recommended system should be 30% ethyl acetate 70%hexane which is less polar than previous one.It will give better separation .

B) 8.5/9.5=0.89

0.89 is the Rf of 3rd compound.

C) The compound which has low Rf are generally polar.

In this case spot no 3 is polar.

2. When solvent front is marked we are able to decide to which  extent the solvent should be moved on TLC. If it is not marked then some times there is a possibility of running over TLC which will result in poor separation .
If we have to run TLC two times in the same solvent system then it is very difficult to remove TLC without marking the solvent front.

3. Small spot have results in less spreading of compound on TLC when it travels along with solvent system. Large spot have high probability to spread which will result in merging of compounds on TLC.

4. After chromatographic separation we have to take TLC of all the test tubes.
Then we have to check the given reaction mixture is separated or not based on their Rf . When we are able to find the test tubes containing same compound showing same Rf from the series of test tube. Those test tubes are selected and combined to evaporate on rotary evaporation.

5. Generally acids are polar in nature so silica has little effect on their movement as silica is also acidic in nature it moderately bonds to acids. Hence generally acids move slowly from silicagel columns. Even some times it will require polar system to remove acid from coloumn.


6. Ethyl acetate is more polar solvent then Hexane, as esters are more polar then long chain compounds. Ethyl acetate as a polar solvent allow better separation of polar compounds because the compounds interact with polar solvents more than non-polar solvents which allows them to elute further on the TLC plate.

And also, Polar dissolve in polar and nonpolar dissolve in nonpolar.

7. Recrystallisation is less time consuming and requires less solvent and gives pure product which will save time and resources for companies hence, crsytallisation is preferred over chromatography.

Add a comment
Know the answer?
Add Answer to:
can you please answer all 1. When you run a TLC of the reaction in ethyl...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • can you please answer all 1. When you run a TLC of the reaction in ethyl...

    can you please answer all 1. When you run a TLC of the reaction in ethyl acetate : hexanes :: 1:1, the plate below is produced. Give a solvent system that would be expected to produce greater separation and a BRIEF (8 words) justification about your choice. (5 points) 9 10 8 7 LLLLLLL 6 5 4 001 2 3 b. Calculate the R for the bottom spot. (5 points) c. Which compound on the TLC plate is the most...

  • 4. Consider the following silica gel TLC plac or compounds A, B, and hexines: developed in...

    4. Consider the following silica gel TLC plac or compounds A, B, and hexines: developed in Fo-o- og a) Determine the Rr values of compounds A, B, and C run on a silica gel TLC plate using hexanes as the solvent b) Which compound, A, B, or C. is the most polar? values if you used acetone instead c) What would you expect to happen to the of hexanes as the eluting solvent? 5) Consider a sample that is a...

  • A TLC plate was run in 1:1 ethyl acetate and hexane, but when developed the plate...

    A TLC plate was run in 1:1 ethyl acetate and hexane, but when developed the plate only showed baseline spots. What change could be made to get the spot(s) to move further up the plate? -Spot a new plate and run again in the same solvent system -Spot a new plate and run in neat hexane -Spot a new plate and run in 1:2 ethyl acetate/hexane -Spot a new plate and run in 2:1 ethyl acetate/hexane

  • d. The following TLC plate was run with a mobile phase that consisted of 5% Ethyl...

    d. The following TLC plate was run with a mobile phase that consisted of 5% Ethyl Acetate:95% Hexanes. Explain the result and describe what change to the mobile phase you would make to correct the issue. Solvent Fruct Speed Compound Line of One

  • If aspirin (acetylsalicylic acid) is used in a TLC experiment with 1:1 Hexanes / Ethyl acetate...

    If aspirin (acetylsalicylic acid) is used in a TLC experiment with 1:1 Hexanes / Ethyl acetate as the solvent system, explain in terms of polarity why the spot would move fast or slow up the TLC plate?

  • 2. A solution containing a mixture of naphthalene, benzoic acid, and benzaldehyde is analyzed via TLC...

    2. A solution containing a mixture of naphthalene, benzoic acid, and benzaldehyde is analyzed via TLC and GC. Use the structures and properties of the compounds to aid in answering the following questions. A. In the TLC experiment, the mixture is spotted on a silica TLC plate and eluted with a 1:1 mixture of hexanes and ethyl acetate. Three spots are observed on the plate, with Re values of 0.25, 0.58, and 0.74. Indicate which spot corresponds to which compound....

  • Common solvents used in TLC analysis are hexane and ethyl acetate, the latter being more polar. A TLC has been performed...

    Common solvents used in TLC analysis are hexane and ethyl acetate, the latter being more polar. A TLC has been performed on a mixture of two compounds. The solvent ran for 3 cm(plate length is 6cm) with 5% ethyl acetate in hexane. The two spots were not resolved, meaning they showed up too close to each other. What can you suggest to possible improve the results of the separation?

  • Possible Quiz Questions 1 What two methods of visualizing spots on a TLC plate will you...

    Possible Quiz Questions 1 What two methods of visualizing spots on a TLC plate will you use in this Give two reasons why would you predict that the elution solvents (hexanes or acetate) would not be visible under UV visualization? week's lab? ethyl 2. Define R 3. Calculate the R of the spot on the following TLC plate. 4. Which compound in each pair is predicted to have the higher Ri? a. CH3CH2CH2CH2OH and CH3CH2CH2CH28r b. CH3CH2CH2CH2OH and CH3CH2CH2CH2CH2CH2CH3 c....

  • A student monitored the reaction progress of the reduction of 4-Nitrobenzaldehyde to 4-Nitrobenzyl alcohol using TLC....

    A student monitored the reaction progress of the reduction of 4-Nitrobenzaldehyde to 4-Nitrobenzyl alcohol using TLC. 30% ethyl acetate in petroleum ether was used as the elution solvent. TLC plates available in the laboratory were coated with the common absorbent silica gel (SiO2.xH2O) which contains polar hydroxyl (OH-) groups. c. The crude product moves slower than the starting material with the mobile phase in the TLC plate. Briefly explain a possible reason for the observation based on the chemical structures...

  • Post-Laboratory Questions Aspirin adnil tuleno Which compound turned out to be the most polar? The least polar? Do...

    Post-Laboratory Questions Aspirin adnil tuleno Which compound turned out to be the most polar? The least polar? Do experimental results agree with your theoretical predictions? If not, why? 2. What would a chromatogram look like if a less polar developing solvent were used 3. Consider the following TLC plate of compounds A, B, and C developed in hexanes: solvent front starting line a) Determine the R values of compounds A, B, and C run on a silica gel TLC plate...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT