User:Eleni N. Kalivas/Notebook/CHEM-571/2013/09/03: Difference between revisions
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==Inosine Protocol== | ==Inosine Protocol== | ||
Using 0.1347 grams of inosine and a 25mL volumetric a stock solution of 0.02M adenosine solution was prepared. The stock solution was then diluted to 4.8e-4 M solution, which was used to create the following dilutions which was prepared to run on the UV-vis. | Using 0.1347 grams of inosine and a 25mL volumetric a stock solution of 0.02M adenosine solution was prepared. The stock solution was then diluted to 4.8e-4 M solution, which was used to create the following dilutions which was prepared to run on the UV-vis. | ||
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|<u>Inosine solution concentrations (M)</u> | |<u>Inosine solution concentrations (M)</u> |
Revision as of 11:26, 3 September 2013
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Objective
Once each group has created a calibration curve we will then determine the standard deviations and the confidence interval, and lastly we will perform a Q-test in order to remove any outlining data. Adenosine ProtocolUsing 0.2006 grams of adenosine and a 50mL volumetric a stock solution of 0.015M adenosine solution was prepared. The stock solution was then diluted to 1.5e-4 M solution, which was used to create the following dilutions which was prepared to run on the UV-vis.
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