Purpose The purpose of this experiment is to determine K, the rate constant k1 of the forward reaction divided by the rate constant k-1, as well as Ymax, which is the maximum number of moles of acetic acid that can be adsorbed on the surface of the charcoal, per gram of charcoal.
Methods A finely powdered charcoal is placed in an acetic acid solution, and some of the acetic acid molecules can be removed from the solution by adsorption on the surface of the charcoal solid. Equilibrium can eventually be established between the acetic acid adsorbed on the surface of charcoal and the unbound acetic acid in the solution. The amount of acetic acid adsorbed onto the surface of the charcoal can be determined through the titration of the original
…show more content…
C is plotted and fitted to a logarithmic-line to illustrate the saturation effect, shown in Figure 1. Then using equation 12.8 in the lab manual, C/Y is calculated and plotted versus C and fitted to a straight line, shown in Figure 2. From the fitted line, Ymax, which is the maximum number of moles of acetic acid that can be adsorbed on the surface of the charcoal per gram of charcoal, can be calculated from the slope. Then, using Ymax and the value of the y-intercept, K, which is the ratio between the rate constant k1 of the forward reaction (adsorption on the charcoal) and the rate constant k-1 (detachment from the charcoal), can be determined. For calculations, refer to Appendix E. Finally, multiplying Ymax by Avagadro’s number will give the number of AA molecules adsorbed on the surface of one gram of charcoal at saturation. Since the approximate surface area occupied by a single AA molecule is 2.1E-19 m2, one can calculate the total surface area of one gram of charcoal. For calculations, refer to Appendix F. Note that all uncertainties from several dilution steps, weighing of the charcoal, the titration steps, and every measurement are taken into account when determining Y and C/Y. The calculated uncertainties are used to draw the error bars on the plots in Figure 1 and Figure
Then more roasting occurred when the crucible was placed into a ceramic triangle for the Bunsen burner to continue its burning for an additional 90 minutes. Once the burning was officially over, the crucible was placed onto a ceramic tile to cool off. Next the charcoal and copper material were poured onto a paper towel and were separated from carefully distinguishing them one from the other. Then comparisons were down through analysis of the copper (II) oxide smelted.
5. Question 5: a) As mentioned in the manual, we have the ratio (K/H+ ), if H+ was lower than K then the equivalent point will be achieved and it will change color. And if H+ was more than K then the solution we are titrating will be the same, the equivalent point won’t be achieved, and it will be acidic solution. And to find the value of H+ is by having the value of pH, therefore the pH has changed from 7 to 9, which is by shifting from 10-7 to 10 -8 by adding the 0.01 of the base, and it will shift again from 10 -8 to 10 -9 by adding another 0.01 of the base to the solution , the different that’s added between the two shifting are close to each other which indicates that the
The compounds tested in included the unknown, Calcium Nitrate, Calcium Chloride, Calcium Carbonate, Sodium Chloride, Potassium Chloride, Magnesium Chloride, and Ammonium Chloride. The next test was the pH test. In this test, the aqueous solutions from the flame tests were used again. A piece of pH paper was dipped into the aqueous solutions, a different piece for each solution. The ensuing coloration of the paper was compared to the pH scale and the
Purpose: The purpose of this lab is to titrate an unknown solid acid (KH2PO4) with a standardized sodium hydroxide solution. After recording and plotting the data, the acid’s equivalence point will be recorded once the color changes. Using the equivalence point, the halfway point will be calculated, which is used to determine the acid’s equilibrium constant. The acid’s calculated equilibrium constant will be compared with the acid’s established pKa value.
Equation 3 was used in this method. It became easier since the value of log10 is equivalent to 1. After Q1 and Q2 were chosen at the H values, the next step is to solve for log Q2/Q1. This calculated value of n came out to be 0.5057. There were also two different methods for solving for the value of K using the best fit line given in Figure 1.
Quinn Nguyen Floating Leaf Disk Photosynthesis Lab Conclusion: Graph your results for all 3 trials on one graph. Label the graph, both axes, and provide a legend to distinguish each trial. What was the rate of photosynthesis for each variable? How many leaves floated per minute? Rate of photosynthesis (leaves/min) Spinach: (2-0)/25 = 0.08
Doriana Spurrell What different frequencies and types of light would prompt the Spinach leaves to go through the process of photosynthesis effectively? Purpose: The purpose of this experiment was to see which of the four lights that range across the light spectrum would properly and most efficiently help the spinach leaf perform photosynthesis. Background Information: Photosynthesis is the process in which plants use light energy to transform into chemical energy.
DIY - What Is Life? How can you determine whether something is alive, dead, or non-living? Whenever we speak of life, we must think in terms of cells.
The topic of research is, “how fast does an Alka-Seltzer tablet make gas?”. In the experiment, the scientists will be measuring the chemical reaction rates that occur, when 1 Alka-Seltzer tablet is placed in a specific temperature of water. The independent variable during the experiment will be the temperature of the water (degrees Celsius). The dependent variable during the experiment will be, the rate in which gas is produced (in seconds). The constants of the experiment, will be the amount of water used and the Alka Selter compound.
Stoichiometry is a method used in chemistry that involves using relationships between reactants and products in a chemical reaction, to determine a desired quantitative data. The purpose of the lab was to devise a method to determine the percent composition of NaHCO3 in an unknown mixture of compounds NaHCO3 and Na2CO. Heating the mixture of these two compounds will cause a decomposition reaction. Solid NaHCO3 chemically decomposes into gaseous carbon dioxide and water, via the following reaction: 2NaHCO3(s) Na2CO3(s) + H2O(g) + CO2(g). The decomposition reaction was performed in a crucible and heated with a Bunsen burner.
CLAIRE MUNTING 29/01/2018 Criterion C EFFECTS OF SURFACE AREA OF CALCIUM CARBONATE UPON RATE OF REACTION Calcium Carbonate Chips 1 Introduction: Within the current investigation, the effects of the surface area of Calcium Carbonate (CaCO3) in combination with Hydrochloric acid (HCl) upon its rate of reaction. CaCO3, commonly referred to as limestone, is an organic substance and is, in a sense, the crystallised “carbonic salt” of the element, calcium2. In addition to being a salt, the pH level of Calcium Carbonate is 9.91, and it is therefore, a basic substance, due to the fact that it is comprised of a pH level higher than 7, which is neutral3. HCl, however, is the bodily acid found in the stomach of human beings.
IV. Data and observations Mass of beaker (g) 174.01 Mass of beaker + NaOH pellets (g) 174.54 Mass of NaOH pellets 0.53 TRIAL 1 TRIAL 2 Mass of potassium acid phtalate (KHP) (g) 0.15 0.15 final buret reading (ml) 30.75
The CO2 gas produced can be used as an indicator for the rate of reaction as the amount of CO2 gas that is collected with in a fixed time is proportional to the rate of reaction. Therefore, the average rate of reaction can be calculated by measuring the amount of CO2 collected for a set period of time. The rate expression of the reaction is written as: rate = k[CaCO3]a[HCl]b 1 http://www.nlm.nih.gov/medlineplus/druginfo/meds/a601032.html 2 http://www.thechemicalblog.co.uk/10-uses-of-hydrochloric-acid/ Page 2 of 7 k represents the rate constant, a and b signify the order of reaction with respect to the reactants. The order of the reaction is the power to which the concentration of that reactant is raised to, for example, doubling the concentration of a reactant that is first order would double the rate of reaction while doubling the concentration of a reactant that is in the second order would quadruple the rate of reaction.
In direct titrations, the number of moles of acid can be easily derived by simply manipulating with the values of acid and base given in the experiment. In back titration, excessive volumes of acid are always added. Of which, only a certain quantity would be neutralised. The number of moles of acid is eventually derived from titrating this excess acid with a strong base and using mole fractions to calculate. The quantity of acid neutralised is obtained by subtracting the moles of acid given at the start of the experiment, with the moles of acid titrated.
Half of this value is 12.63 mL. By interpolating the graph, the pH at this volume was 4.80, which is equivalent to the pKa of acetic acid. According to the tabulated data, the pKa was 4.90 at 15 mL of NaOH. At this point, the change in pH with respect to volume was minimal since these values were far from the equivalence point, which occurred experimentally at 27.41 mL. This can also be seen on the graph as the plateau before the inflection point occured. To calculate the Ka of the acid, the following formula is