Question

Suppose you are trying to separate a mixture of compounds using reversed-phase liquid chromatography (RPLC). On...

Suppose you are trying to separate a mixture of compounds using reversed-phase liquid chromatography (RPLC). On the first run, using a mobile phase containing 40% tetrahydrofuran and 60% water, the peaks all elute between 0 and 3 min and are too close together to be quantitatively resolved. To improve the resolution of the peaks, should you increase or decrease the amount of water in the mobile phase for the next run? Or is there not enough information?

In a separate experiment, you are trying to separate a mixture of compounds using normal-phase liquid chromatography (NPLC). On the first run, with a mobile phase containing 35% toluene and 65% acetonitrile, the peaks again eluted quickly and were poorly resolved. To improve the resolution of the peaks, should you increase or decrease the amount of acetonitrile in the mobile phase for the next run? Or is there not enough information?

Homework Answers

Know the answer?
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
Similar Questions
If two bands are not fully resolved in a reverse-phase liquid chromatography experiment when using a...
If two bands are not fully resolved in a reverse-phase liquid chromatography experiment when using a mobile phase of 50:50 water: acetonitrile, which of the two components of the mobile phase should you increase the percentage of in order to improve the resolution? Explain how this change will improve the peak separation?
Suppose you are using adsorption chromatography to elute a mixture of compounds bound to alumina gel....
Suppose you are using adsorption chromatography to elute a mixture of compounds bound to alumina gel. The mobile phase is cyclohexane. Some compounds remain bound to the column; what change of mobile phase might you use to elute the compounds? Explain your answer.
You are trying to separate a mixture of Glutamate, Asp, and Leu. You run the mixture...
You are trying to separate a mixture of Glutamate, Asp, and Leu. You run the mixture over an anion exchange column (buffer pH = 6.0). In what order should the amino acids elute? Hint: Consider the side chain pKas
How would you separate a mixture of benzhydrol, benzophenone, and biphenyl using column chromatography (i.e. which...
How would you separate a mixture of benzhydrol, benzophenone, and biphenyl using column chromatography (i.e. which is the best eluent or mixture of eluent, order of addition of the eluents, order of elution, ect.)?
A student separated two unknown compounds using Fractional Distillation followed by Gas Chromatography. The GC column...
A student separated two unknown compounds using Fractional Distillation followed by Gas Chromatography. The GC column had a non-polar liquid stationary phase and Helium was the mobile phase. Using the following data, determine the identity, boiling point and percent composition for each of the compounds in the GC sample. Explain reasoning. Your left peak has a percent composition of 20.49% and the right has 79.6%. Hexane boiling pint is 69.2 Heptane boiling boing is 98.5 Methanol is 65.1 Octane 126...
1. If you load the mixture of compounds using more than a "minimal amount of CH2Cl2",...
1. If you load the mixture of compounds using more than a "minimal amount of CH2Cl2", what will happen to your separation? A. The seperation will be poor since CH2Cl2 is a less polar solvent than petroleum ether. B. The seperation will be improved since CH2Cl2 is a more polar solvent than petroleum ether C. The seperation will be improved since CH2Cl2 is a less polar solvent than petroleum ehter D. The seperation will be poor since CH2Cl2 is a...