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Abstract for chemical kinetics lab report
Principles of chemical kinetics
Principles of chemical kinetics
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Discussion Objectives: This experiment is monitoring the reaction of sodium hydroxide and crystal violet using spectroscopy. Graphical methods will be used to determine the kinetic rate law, rate constant and activation energy for the reaction. General Discussion: The order of hydroxide was determined by the varying the initial concentration of hydroxide in runs 1 and 2. We used the isolation method, which calls for having much higher concentrations of one reactant then the other, in this case the concentration of NaOH being much higher than the concentration of Crystal Violet. This method allows to be converted to where . kobs was determined by linearizing the data for absorbance with regards to time, with the slope of the linearized graph being kobs. The equation for reaction 1 was then divided by the same equation for reaction 2, allowing for a calculation of n which was approximately 1. The order of crystal violet was calculated by graphing absorbance with regard to time for the first set of data. Since the spectrometer was set to detect crystal violet and according to Beers law concentration is proportional to absorbance, this data is proportional to the concentration of Crystal Violet. In plots …show more content…
The first possible source of error is the assumption that [OH-] does not change over the course of the experiment, even though it does. However, since the order of magnitude of [OH-] is so large compared to [CV] this error is miniscule. Another possible error is inaccuracies in the spectrometer, and for the calculation of the order of OH-, the measurement of the initial concentrations of the reactants. While these sources of error probably did contribute to slight differences in concentration, they were consistent and small enough to have little impact on the calculation of order, which is demonstrated by the extremely high R2 values (R2 >.999) for the graph of natural log of absorbance versus
The analyzed yellow#5 wavelength was determined to 395nm because the actual wavelength 427nm was restricted in the Micro lab. The R2 value of the graph is 0.9827, and the level of data accuracy it indicated extremely weak data correlation. The first one dilution data points excluded from the standard curve because the point is not in the linear curve. The first concentration and absorbance value are the highest point in the graph that cannot connect as linear with another data point. After removing the first data point, the standard curve is clear and make
Absorbance was defined as: log I_o/I where I_o is incident light and I is the transmitted light. Fluorescence emission spectrum is different from fluorescence excitation spectrum because it records different wavelengths of chemical s...
The mean for the temperatures is 0.116 and the solvents is 20. We predicted the 37 Celsius would be the most absorbed, but it was the -20 Celsius which can be seen in the graph above.
Experiment: First prepared a well plate with the appropriate amounts of distilled water, HCl, and Na2S2O3 in each well according to the lab manual. The well where the reaction
These are both needed for the equation that will give the rate constant, k: ln([RCl]0 ÷ [RCl]t) = kt. The initial concentration was found with the formula [RCl]0 = (V ͚ - V0) , and the concentration at time t was found by [RCl]t = (V ͚ - Vt). These equations were derived after the reaction volume and NaOH concentration canceled out. Since the reaction was first order, plotting ln([RCl]0 ÷ [RCl]t) versus time, the slope will equal the specific rate constant, k. After plotting the data for both the kinetic runs, the second kinetic run had a greater rate constant of 0.0018 compared to 0.0007 in the first kinetic run. Therefore, the data reflected that the more polar solvent resulted in a faster reaction and a greater rate constant, which is characteristic of an SN1 reaction. The polar solvent solvates the carbocation, which lowers the energy and increases the stability of the carbocation. An increase in stability of the carbocation causes an increase in the rate of formation of the carbocation, therefore, increasing the rate of the reaction. Overall, the experiment was successful in testing the effects of solvent polarity, however some sources of error could have affected the data. For example, the recorded times of when the solution turned green or the amount of NaOH added could have been
...eases, including temperature. It is determined from the data that the reaction is more likely to have a step wise mechanism than a concerted due to the small – ΔS and a relatively large value of ΔH from the tables. Due to some errors, it is best to perform another experiment for future protocols. In addition with the variance the 35°C where at one point the absorbance levels off and then increases. In comparison to the rate constant against temperatures, at 25°C it is higher than 35 and 45. More test is required to ensure proper determination of the rate constant at those temperatures.
This specific lab will focus on the two main variants of Atomic Absorption Spectroscopy: flame AA spectroscopy, and spectroscopy using a graphite furnace. The lab will also introduce and teach how to deal with both systematic and random error when using Atomic Absorption Spectroscopy.
2. In order to determine how fast a reaction is occurring there must be a basis for measurement. There must also be an indicator substances to determine the change that took place. Then there must be a tool to measure the change. In this lab a spectrophotometer was used. The ABS value is the actual value and it is used to determine the rate of change.
One possible source of experimental error could be not having a solid measurement of magnesium hydroxide nor citric acid. This is because we were told to measure out between 5.6g-5.8g for magnesium hydroxide and 14g-21g for citric acid. If accuracy measures how closely a measured value is to the accepted value and or true value, then accuracy may not have been an aspect that was achieved in this lab. Therefore, not having a solid precise measurement and accurate measurement was another source of experimental error.
Compared to the 0.5 M hydrochloric acid that was less concentrated, the more concentrated 2 M hydrochloric acid c...
A cuvette was filled 3/ 4ths of the way and the absorbance measured in a spectrophotometer. The data was compiled as a class and recorded. The Spectrophotometer was blanked using a test tube of distilled water.
The Results obtained from the experiment proved the original theory at the start of the experiment. The results table clearly shows pigment levels increasing with the rinsing temperature increments.
In this experiment three different equations were used and they are the Stoichiometry of Titration Reaction, Converting mL to L, and Calculating the Molarity of NaOH and HCl (Lab Guide pg. 142 and 143).
As we already now know, Spectroscopy is the study of how light is emitted, absorbed and scattered through a material source. In the world of science many different types of Spectroscopy exists, but for this assignment I will only be speaking of five types, which include, Infrare...
There is also the potential of human error within this experiment for example finding the meniscus is important to get an accurate amount using the graduated pipettes and burettes. There is a possibility that at one point in the experiment a chemical was measured inaccurately affecting the results. To resolve this, the experiment should have been repeated three times.