Spectrophotometry question - anyone experienced with it?

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In summary, the speaker is conducting an experiment to find the equilibrium concentration for the reaction between Fe 3+ and SCN-. They have already graphed a calibration curve and found the constant for absorption and concentration. The next part of the experiment involves using a constant volume of Fe 3+ and varying the volume of SCN-. The speaker is unsure if the equilibrium concentration will be the same for all trials with different volumes of one of the reactants, but their calculations for the equilibrium constant have all been roughly the same except for one trial with a lower volume of one of the reactants. They are also questioning if there may be experimental error associated with the spectrophotometry device they are using.
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omgwtfitsp
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Hey guys, I'm doing an experiment trying to find the equilibrium concentration for the reaction:

Fe 3+ + SCN- = FeSC 2+

So now, I have already graph the calibration curve and found the constant for absorption and concentration.

This next part of the experiment we use a constant volume of Fe 3+ but change the volume of SCN -

So I have to find the equilibrium concentration for the product (FeSCN 2+) for each trial of different volumes.

So would we expect the equilibrium to be the same for all the trials with the different volumes one of the reactant or should they be different?

Because when I calculated the equilibrium constant for each trial, they all roughly came to about the same number, off by a bit here and there. Except for the first test tube that had the lowest volume of one of the manipulated reactant, this trial had a higher constant than the others.

I'm not familiar so much with spectrophotometry, so is there some experimental error that is associated with this device?
 
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  • #2
Not sure exactly what data you have, but absorbance is directly related to concentration of the complexed iron. You can recalculate the absorbance for constant volume. In other words, if you are adding volume increments of your ligand solution then you are increasing the volume of your resulting solution of the the complex. If you were adding only the ligand without its amount of volume of solvent, then your absorbance would be higher. In reality, you will include solvent WITH the added ligand, therefore, you should make a recalculation of absorbance.
 

Related to Spectrophotometry question - anyone experienced with it?

1. What is spectrophotometry and what is it used for?

Spectrophotometry is a technique used to measure the amount of light absorbed by a sample at different wavelengths. It is commonly used in scientific research and various industries to analyze the concentration of chemicals in a solution.

2. How does spectrophotometry work?

In spectrophotometry, a light source passes through a sample and the amount of light that is absorbed is measured by a detector. The results are then compared to a standard curve or known values to determine the concentration of the sample.

3. What are the different types of spectrophotometers?

There are several types of spectrophotometers, including UV-Vis, fluorescence, and infrared spectrophotometers. Each type uses different wavelengths of light and detection methods to analyze samples.

4. What are the key factors to consider when using spectrophotometry?

Some important factors to consider when using spectrophotometry include selecting the appropriate wavelength for the sample, ensuring the sample is properly prepared and free of contaminants, and following the manufacturer's instructions for the specific instrument being used.

5. What are some common sources of error in spectrophotometry measurements?

Sources of error in spectrophotometry measurements can include improper sample preparation, inaccurate calibration of the instrument, and interference from other substances in the sample. It is important to carefully control these variables to ensure accurate results.

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