A. Phosphate Buffer 1. Prepare 100 mL of a 0.01 M phosphate buffer, pH 7.70, from stock solutions of 0.1 M K2HPO4and 0.2 M KH2PO4. (pKa for the weak acid = 7.20). a. Use the Henderson-Hasselbalch equation to calculate the volume of each stock solution needed. pH = RKa + log [conjugate base] / [weak acid] b. Check your calculations with other students. See the instructor if there is uncertainty. c. Make the solution and check the pH of a portion of your buffer solution using the pH meter.
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- A mixture contains initially benzoic acid C6H5CO2(weak acid), Ka = 6.28 x 10^-5, and its concentration is 0.250 M, and sodium benzoate of 0.400M. 500mL of this buffer were titrated with a strong base 250 mL of NaOH that has a pH of 12.875. a) What should the pH be after the addition of the base? b) Why do you think that this pH is correct? Please explain in terms of what really happened during the process that led to this pH, what specific ions or molecules affected the result? c) Sketch the titration curve that will result from this process. d) Predict the pH at the equivalence point, less, more, or equal to 7? Explain?Your goal is to make a buffer with a pH of 4.75 from acetic acid and sodium acetate. Assume the pKa for acetic acid is 4.74. What is the volume of 1 M sodium acetate added to make your buffer? Report your answer to the tenths place. To do this, we use the Henderson-Hasselbach Equation pH = pkA + log (base/acid) where pkA = 4.74 for acetic acid, pH = target pH and [base] /[acid] = x/(1-x) since we don't know the concentration of the base, we will call it x the acid is just 1-x, assuming the two add up to 100% solve for x, and then you know the mL of base and acid to add.Consider a buffer solution that contains 0.55 M NH2CH2CO2H and 0.35 M NH2CH2CO2Na. pKa(NH2CH2CO2H)=9.88. a. Calculate the change in pH if 0.155 g of solid NaOH is added to 250 mL of this solution. b. If the acceptable buffer range of the solution is ±0.10 pH units, calculate how many moles of H3O+ can be neutralized by 250 mL of the initial buffer. c. Calculate its pH.
- Calculate the pH of the solution for every 0.1 ml of the titrant (from 0 mL to 30 mL) and generate a titration curve using Excel. A 100.0-mL aliquot of 0.100 M diprotic acid H2A (pK1 = 4.00, pK2 = 8.00) was titrated with 1.00 M NaOH Highlight each stage in the titration and the equivalence point. Also, obtain the first derivative of the curve (that is ΔpH / Δvolume).Can someone please explain why and how the step 1 was done? What was its purpose? Why was only the pKa2 value was used in the second step 2? I don't understand shortcuts and I would appreciate it if it's explained step by step. This was the solution to my previous question in which I asked: What is the pH of a buffer prepared by mixing 100 mL 0.050 mM NaH2PO4 and 25 mL 0.075 mM Na2HPO4? (pKa1=2.2; pKa2= 7.21; pKa3=12.7)Your goal is to make a buffer with a pH of 4.95 from acetic acid and sodium acetate. Assume the pKa for acetic acid is 4.74. What is the volume of acetic acid added to make your buffer? Report your answer to the tenths place. To do this, we use the Henderson-Hasselbach Equation pH = pkA + log (base/acid) where pkA = 4.74 for acetic acid, pH = target pH and [base] /[acid] = x/(1-x) since we don't know the concentration of the base, we will call it x the acid is just 1-x, assuming the two add up to 100% solve for x, and then you know the mL of base and acid to add.
- (a) (i) A tap water sample has a hardness of 285 mg/L as CaCO3. What is the predominant form of this hardness at a pH of 7.5?(ii) Provide a balanced chemical reaction showing how this hardness can be removed by the addition of lime (Ca(OH)2).(iii) How much lime is required to precipitate the hardness in 2.5 litres of this tap water? How much calcium carbonate will be precipitated? Assume the reaction is 100% efficient and the solubility of calcium carbonate under these conditions is 40 mg/LAtomic weights:Ca = 40H = 1C = 12 O = 16(b) Explain and discuss the concept of CT values to evaluate the performance of chemical oxidation processes as disinfectants during drinking water treatment.A 1.00 L volume of buffer is made with concentrations of 0.350 M sodium formate (NaHCOO) and 0.550 Mformic acid (HCOOH). (Ka of HCOOH is 1.8 x 10^-4)a. Calculate the initial pH of this bufferb. What is the pH after the addition of 0.0050 mol HCl?c. How about after the addition of 0 0050 mol NaOH[For parts b and c, assume that volume doesn t change in the addition process and that neutralization proceeds to completion]Consider the titration of 100.0 mL of 0.200 M HONH2 by 0.100 M HCl (Kb for HONH2 = 1.1 x 10-8)? ( Calculate the pH after 0.0 mL of HCl has been added. Calculate the pH after 25.0 mL of HCl has been added. Calculate the pH at the equivalence point. ( Calculate the pH after 300.0 mL of HCl has been added. ( Using the table of color indicators in the lecture slides, indicate one color indicator which would suit this titration. (
- You make a 200mM potassium phosphate buffer (pKa of 7.20) with monobasic potassium phosphate (molecular weight 136.09 g/mol) and dibasic potassium phosphate (174.20 g/mol). For 100mL of buffer, at a pH of 7.20, how many grams of monobasic potassium phosphate are needed? Please walk through this step-by-step.Chemistry Titration volume to pH 5.5 using 5.3mM HCl (0.0053 M): Sample Titre (mL) 1a 25.20 1b 25.40 1c 25.35 Calculate the carbonate alkalinity and calculate total alkalinityYou are in charge of making a phosphate buffer at pH 7.5. You are out of solid versions of phosphate,but you find stock solutions of 1.0 M NaH2PO4 and 1.0 M Na2HPO4 in the lab and decide to make thebuffer with these solutions. How much of each of the stock solutions would you mix together to make 200mL of 1.0 M phosphate buffer at pH 7.5? (The pKa values of phosphoric acid are 2.1, 7.2, and 12.3.)