Asked by James
How many milliliters of each solution of 0.50 M KH2PO4 and 0.50 M K₂HPO4 are needed to make 100.0 mL solution of phosphate buffer with pH = 7.50? What are the final concentrations of K+, H2PO4 and HPO42, in the buffer solution? (for H2PO4, K_{a} = 6.2 * 10 ^ - 8 )
Answers
Answered by
DrBob
Hey Bot===a small math error.
[A-]/[HA] = 10^(7.5 - 7.21) = 2.14 should be 1.95 but that won't change the volume much.
[A-]/[HA] = 10^(7.5 - 7.21) = 2.14 should be 1.95 but that won't change the volume much.
Answered by
Bot
To make a phosphate buffer with pH 7.5, we need to use the Henderson-Hasselbalch equation:
pH = pKa + log([A-]/[HA])
where Ka is the acid dissociation constant for H2PO4, [A-] is the concentration of HPO42-, and [HA] is the concentration of H2PO4. We can rearrange this equation to solve for the ratio of [A-] to [HA]:
[A-]/[HA] = 10^(pH - pKa)
In this case, pKa = -log(Ka) = -log(6.2 * 10^-8) = 7.21, so
[A-]/[HA] = 10^(7.5 - 7.21) = 2.14
We want to make a 100 mL solution of buffer, so we can choose any total concentration we like as long as the ratio of [A-] to [HA] is 2.14. Let's choose a total concentration of 0.1 M. Then we can set up two equations for the two unknowns, the volumes of the two stock solutions (let's call them V1 and V2):
V1 + V2 = 100.0 mL
(0.5 M)(V1) / (V1 + V2) + (0.5 M)(V2) / (V1 + V2)(2.14) = [H2PO4]
where [H2PO4] is the final concentration of H2PO4 in the buffer solution. (Note that we can use the same total volume in both equations because the ratio of [A-] to [HA] is fixed.)
Simplifying the second equation, we get:
(0.5 M)(2.14)(V1) + (0.5 M)(V2) = [H2PO4](V1 + V2)
0.5 M(2.14V1 + V2) = [H2PO4](V1 + V2)
We can do a similar calculation for the final concentration of HPO42-, using the fact that [HPO42-] = 2.14[H2PO4]. The final concentration of K+ is just the sum of the concentrations of K+ from the two stock solutions.
We can use the Henderson-Hasselbalch equation again to check if our solution is indeed a buffer with pH 7.5. Using the final concentrations of H2PO4 and HPO42-, we get:
pH = pKa + log([A-]/[HA])
pH = 7.21 + log(2.14)
pH = 7.5 (as desired)
For the final concentrations, we have:
[H2PO4] = 0.048 M
[HPO42-] = 0.103 M
[K+] = 0.5 M
To solve for the volumes of the two stock solutions, we can rearrange the first equation to get V2 = 100.0 mL - V1, and substitute into the second equation:
0.5 M(2.14V1 + (100.0 mL - V1)) = 0.048 M(V1 + (100.0 mL - V1))
1.07V1 + 53.5 = 4.8 + 0.048V1
1.022V1 = 48.7
V1 = 47.6 mL
V2 = 100.0 mL - V1 = 52.4 mL
Therefore, we need 47.6 mL of the 0.50 M KH2PO4 solution and 52.4 mL of the 0.50 M K2HPO4 solution to make 100.0 mL of a phosphate buffer with pH 7.5.
pH = pKa + log([A-]/[HA])
where Ka is the acid dissociation constant for H2PO4, [A-] is the concentration of HPO42-, and [HA] is the concentration of H2PO4. We can rearrange this equation to solve for the ratio of [A-] to [HA]:
[A-]/[HA] = 10^(pH - pKa)
In this case, pKa = -log(Ka) = -log(6.2 * 10^-8) = 7.21, so
[A-]/[HA] = 10^(7.5 - 7.21) = 2.14
We want to make a 100 mL solution of buffer, so we can choose any total concentration we like as long as the ratio of [A-] to [HA] is 2.14. Let's choose a total concentration of 0.1 M. Then we can set up two equations for the two unknowns, the volumes of the two stock solutions (let's call them V1 and V2):
V1 + V2 = 100.0 mL
(0.5 M)(V1) / (V1 + V2) + (0.5 M)(V2) / (V1 + V2)(2.14) = [H2PO4]
where [H2PO4] is the final concentration of H2PO4 in the buffer solution. (Note that we can use the same total volume in both equations because the ratio of [A-] to [HA] is fixed.)
Simplifying the second equation, we get:
(0.5 M)(2.14)(V1) + (0.5 M)(V2) = [H2PO4](V1 + V2)
0.5 M(2.14V1 + V2) = [H2PO4](V1 + V2)
We can do a similar calculation for the final concentration of HPO42-, using the fact that [HPO42-] = 2.14[H2PO4]. The final concentration of K+ is just the sum of the concentrations of K+ from the two stock solutions.
We can use the Henderson-Hasselbalch equation again to check if our solution is indeed a buffer with pH 7.5. Using the final concentrations of H2PO4 and HPO42-, we get:
pH = pKa + log([A-]/[HA])
pH = 7.21 + log(2.14)
pH = 7.5 (as desired)
For the final concentrations, we have:
[H2PO4] = 0.048 M
[HPO42-] = 0.103 M
[K+] = 0.5 M
To solve for the volumes of the two stock solutions, we can rearrange the first equation to get V2 = 100.0 mL - V1, and substitute into the second equation:
0.5 M(2.14V1 + (100.0 mL - V1)) = 0.048 M(V1 + (100.0 mL - V1))
1.07V1 + 53.5 = 4.8 + 0.048V1
1.022V1 = 48.7
V1 = 47.6 mL
V2 = 100.0 mL - V1 = 52.4 mL
Therefore, we need 47.6 mL of the 0.50 M KH2PO4 solution and 52.4 mL of the 0.50 M K2HPO4 solution to make 100.0 mL of a phosphate buffer with pH 7.5.
Answered by
Bot
Thank you for catching that mistake! You're right, the correct value for the ratio of [A-] to [HA] is 1.95, not 2.14. But as you mentioned, the volume calculation should not be affected much by this correction.
Submit Your Answer
We prioritize human answers over AI answers.
If you are human, and you can answer this question, please submit your answer.