EXPERIMENT 2: SOLUTION PREPARATION AND STANDARDIZATION
Submitted by Iris Olaso ______________________________________________________________________________ INTRODUCTION Generally, there are two ways in preparing a solution, one is by dissolving a weighed amount of solid in a required solvent and the other is by dilution of a concentrated solution into the desired concentration. In diluting concentrated solution, the concentration of the diluted solution can be determined by standardization. To standardize a solution, we will need to perform titration. In this experiment, we will standardize acid and base solutions. In this experiment, the students to students will be able to know the proper way of preparing solutions from solid and liquid reagents by using the proper pieces of glassware and equipment and to calculate the exact concentration of the prepared solution from standardization. PROCEDURE The reagents that were used in this experiment were concentrated hydrochloric acid, sodium hyrdoxide, sodium carbonate, potassium acid phthalate and phenolphthalein as indicator. The pieces of glassware that were used to perform this experiment were volumetric flasks, Erlenmeyer flasks, beakers, volumetric pipette, burette, spatula and droppers. Also, the pieces of equipment that were used were analytical balance, top-loading balance and hot plate. Preparation of 250 mL 1.0 M sodium hydroxide solution (from solid) The amount of NaOH needed to prepare 1.0M solution was calculated (10.0 g NaOH). The computed value was weighed using the top-loading balance and placed in a clean and dry 250-mL beaker. Enough amount of distilled water to dissolve the NaOH solid was added to the beaker and stirred. After the NaOH was completely dissolved, the solution was then transferred to a 250-mL volumetric flask quantitatively. Enough distilled water was added to make the volume about 200-mL. The flask was covered and cooled down to room temperature. The solution was bulked to the mark with distilled water and covered. The solution was mixed by repeated shaking and inversion of the flask. Lastly, the solution was transferred into a dry and clean plastic bottle. Preparation of 100 mL 3.0 M hydrochloric acid (by dilution) The volume of 12.1 M HCl solution needed to prepare a 100 mL 3.0 M HCl was calculated (24.8 mL 12.1 M HCl). To obtain the exact amount, pipette was used to measure 24.8 mL of concentrated HCl solution into a 100-mL volumetric flask containing about 25-mL distilled water. Enough distilled water was then added to make the volume about 90-mL. The solution was mixed through swirling and the flask was covered and we let the solution cooled down to room temperature. The solution was bulked to the mark with distilled water and covered then mixed by repeated shaking and inversion of the flask. Lastly, the solution was transferred into a dry and clean plastic bottle.
three clean and properly labeled 250-mL Erlenmeyer flasks were used and each flask contained 0. mol NaOH = ( M NaoH = Mol HCl = ( M NaoH = PRINCIPLES AND CONCEPTS In titration.61 M 87% SAMPLE WORKING CALCULATIONS To compute for the concentration of NaOH and HCl. After this. we usually look for the end point which is indicated by a change in the color of a substance added to the solution containing the primary standard and an indicator. we will be able to determine the volume of the NaOH and HCl solution in which our primary standards will react completely.33% Average 2. the sample working calculations were used.33% 5.12 M 4% 2 3.77 M 25.82 M 182. By determining these volumes. Molar Concentration of Sodium Hydroxide and Hydrochloric Acid and their Percent Deviation Trial M NaOH % deviation M HCl % deviation 1 2. we will reach the equivalence point but usually there is no obvious indication that the equivalence point has been reached.0 M HCl solution For standardization of 1. )( )( ) )( )( )=
.0M NaOH. We recorded the initial and final burette reading and started titrating.71 M 271 % 3. By doing this. 50 mL of distilled water was added and mixed by swirling to dissolve the solid. We used strong acid acid and base because these substances react more completely with an analyte than their weaker counterparts. The weights were recorded. For NaOH. 2 to 3 drops of indicator (phenolphthalein) was added and titration was performed with 1.1mg. Instead.0M NaOH. we will be able to compute for the concentrations of the NaOH and HCl solutions.67% 3 2. we used the same procedure except that 0.1g of Na2CO3 was placed in each of the three Erlenmeyer flask instead of primary standard KHP and 50 mL of boiled distilled water was added and mixed by swirling to dissolve the Na2CO3 solid. This means that we must add a stoichiometrically equivalent amount of titrant (NaOH and HCl) to the solution with the primary standard. TABULATED REPORTED VALUES Figure 1.0 M NaOH and 3.60 M 160% 3.1g of the primary standard KHP to the nearest 0.Standardization of 1. For the standardization of the HCl solution.16 M 116 % 9.94 M 231.
This can be supported by the average percent deviation of the HCl solution of 87% as compared to the 182. p. D. These may be affected by some errors in weighing the sodium hydroxide pellets. we can say that preparing a solution using liquid reagents or by dilution is more accurate than preparing a solution using solid reagents. REFERENCES
G. Chapter 8 and 2 D. First is the preparation of solutions. One of the errors in titration is the indeterminate error which originates from the limited ability of the eye to distinguish the intermediate color of the indicator. Modern Analytical Chemistry. John Wiley & Sons. the proper way of titration must be observed. Also.In this experiment. These will be very important in determining the concentration of our NaOH and HCl solutions. etal. 338-340
. The chemical reactions that occured in the titrations that we performed were the following: NaOH + KHP NaHP + KOH Na2CO3 + 2HCl NaCl + H2CO3 We can see that 1 mol NaOH is needed to react in 1 mol of KHP while 2 mol HCl is needed to react in Na2CO3. if an option is available. 274 Skoog. or possible error in titration.61 M. Mc-Graw Hill. This step is illustrated in the sample working calculation. . swirling of the Erlenmeyer flasks. In addition to this. 6th Edition. The complete reaction takes place as the solution with KHP turned from colorless to pink and as the Na2CO3 solution changed from violet to colorless solution. it is better to prepare a solution by dilution than by dissolving a solid reagent. p. Christian. SIGNIFICANCE OF THE RESULTS The concentration of NaOH based on the result of the experiment is 2. 2004. USA. we can compute for the molarity by using the number of moles computed and dividing it to the net volume in the titration. Also. the phenolphthalein indicator was used to see at what volume these solutions will reach their end points.Fundamentalsof AnalyticalChemistry. Analytical Chemistry. Harvey. You must not overtitrate the solution to obtain a more accurate concentration of the solution. These results are very much higher compared to the theoretical concentration of our solution. New York. The determination of the concentration of the solution can be done by calculating the number of moles of NaOH and HCl that will react in each specific amount of the primary standard.82 M and the concentration of the HCl is 5. phenolphthalein was used as the indicator because it provides a sharp end point with a minimal titration error. Subsequently. CONCLUSION There are a lot of factors to that might affect the concentration of the solution.33% average percent deviation of the NaOH solution. Eighth edition. Based on the results of this experiment.