In lab we have to determine how much red 40 is in the kool aid using standard addition. We plotted are data points and got y = 8.7119x+0.1037 The abosrbance of the kool aid was 1.070 and the absorbance of the red 40 was 1.058. For the kool aid we diluted .10 mL of the red 40 in 10 mL beofre putting through column to get data points. HOw do I find the cocnentration of the red 40 in the kool aid mix (0.5032 g). Then how much red 40 is in the entire kool aid packet (3g)?
0.1 mL in 10 mL indicates the dilution factor is 1:100
i.e. 1.058+1.070 = 8.7119x + 0.1037
Therefore, x = The concentration of all the sample = 0.23236 M
Here, the concentration of red 40 should be greater than 0.23236 M because it is the whole concentration.
i.e. The concentration of red 40 = 0.23236*10/0.1 = 23.236 M
In lab we have to determine how much red 40 is in the kool aid using...
Isopop) Pre-Lab Assignment: According to the nutritional label, the dyes in Grape Kool Aid are Red-40 and Blue-1. • Draw Lewis Dot Diagrams for Red-40, and Blue-1. (Abbreviated structural diagrams for the dyes are acceptable. Cite sources!) • Draw Lewis Dot Diagrams for each solvent: isopropyl alcohol, water, ethanol, and acetone. Label the intermolecular forces present in each molecule. Based on the structures, develop a CLAIM for each experiment: • For the paper chromatography portion, your claim will involve relative...
How do I calculate the concentrations for my data sheet lab. I
have not started my lab yet but I just need to see how i would
calculate it with absorbance. Do i just use Beer's law or is there
any other method of solving the concentrations.
7. Weigh 1.45-1.55 g of copper(I) sulfate pentahydrate in a 50 mL beaker. 8. Dissolve the copper(II) sulfate pentahydrate in -15 mL of water 9. Add the aqueous solution of copper(II) to a...
Beer’s Law Objective : We will explore an application of absorption spectroscopy using calibration curves and Beer’s Law. Use the “LAB : HOW TO…” link from the class website if you need help with how to use balance, Bunsen burner… and such. Introduction: You may write this information in your lab notebook for your own reference. It can’t be cut and pasted. Different solutions have different spectral properties. In this portion of the experiment those properties will be utilized to...
Please help guide or explain how I would graph this? Thank you
so much
IV. Data Table • Fill in the remaining columns on your data table. Calculate the solubility at each temperature by dividing the mass of KNO, used by the volume of solution at that temperature. (Watch sig tig! V. Graphing the data - Temperature (°C) on the x-axis and Solubility (g KNO/mL solution) on the y-axis • Orient graph paper as noted "up" with long dimension on...
Hi
I am im a biochemistry lab and we are doing an experiment titled:
PCR Amplification of LeuRS F C Terminal Domain. I am having
troubles figuring out the rest of my caluclations.
I already did the calculations for the first dilution set, I
was wondering how I would do the calculation for the second
dilution set.
Also I was wondering how I would determine the theoretical
values for my data. Is there a specific formula I can use?
If...
Answer the questions using the data and graph. please show all
work. Thank you
Titration of Hydrochloric Acid: 1) Use the buret that is located near the hydrochloric acid container to dispense 25.00 mL of hydrochloric acid solution into a clean dry 100 mL beaker. Record the molarity of this solution on your data sheet. 2) Check to make sure that the volume on your sodium hydroxide buret reads 0.00 mL. If it does not read 0.00 mL, adjust it...
Bio 121
I need to make (yeast fermentation) lab
report.
This is the lab experiment and results:
This is a guide to making the lab report:
General Biology BIO121 Yeast Fermentation Lab Introduction Organisms stay alive by the utilization of energy through metabolism. The energy acquiring pathways in photosynthesis convert radiant energy from the sun into the chemical bond energy of carbohydrates. This photosynthetic process is limited to the producers or autotrophs, which include plants, photosynthetic bacteria and some protists....
just one example/demonstration!
Data needed to be calculated is in highlighted in green boxes.
And I highlighted in red an equation (not sure if thats what you
use to calculate it) And ignore the lab instructions on completeing
a graph!! I already know how to do that in excel, just curious how
Ln (relative rate) and 1/T in K^-1 is calculated by hand*
here is the rest of that lab leading up to the question as I
know its typically...
For the preparation and standardization of NaOH with KHP im supposed to boil water for 1hr and 30 min to remove CO2....the problem is that if I don't boil it for that long and (30 min) b/c of not enough time but I put the water I boiled for 1/2 hr aproximately into a NaOH bottle with a CO2 absorber and stored it there for a few days. I would assume that I would have to boil the water again...but...