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Citrus2011 [14]
3 years ago
10

You have 0.500 L of an 0.250 M acetate buffer solution (i.E. [HC₂H₃O₂] + [C₂H₃O₂⁻] = 0.250 M) at pH 3.50. How many mL of 1.000 M

NaOH must you add in order to change the pH to 5.25? Acetic acid has a pKa of 4.74.
Chemistry
1 answer:
adelina 88 [10]3 years ago
3 0

Explanation:

Relation between pH and pK_{a} is as follows.

            pH = pK_{a} + log \frac{[CH_{3}COO^{-}]}{[CH_{3}COOH]}

Hence, total moles of acetate is calculated as follows.

           0.250 M \times 0.5 L

           = 0.125 M

     \frac{B}{A} = 10^{{pH} - pk_{a}}

                 = 10^{3.50 - 4.74}

                 = 0.0575

Let us assume that there are x moles of acid. Hence, moles of B are as follows.

                 B = (0.125 - x) moles

      \frac{0.125 - x}{x} = 0.0575

                  x = 0.118 moles

Now, we will calculate the concentration as follows.

           5.25 = 4.74 + log \frac{[B]}{[A]}

           log \frac{[B]}{[A]} = 10^{5.25 - 4.74}

                        = 3.236

                     x = \frac{0.125}{4.236}

                         = 0.0295 moles

Therefore, moles of NaOH needed to add are as follows.

        M_{NaOH} \times V_{NaOH} = (0.118 - 0.0295) moles

          1.00 M \times V_{NaOH} = 0.0885 moles

                            = 0.0855 L \times \frac{10^{3}ml}{L}

                            = 88.5 ml

Thus, we can conclude that there is 88.5 ml of 1.000 M NaOH must you add in order to change the pH to 5.25.

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Consider the titration of 100.0 mL of 0.280 M propanoic acid (Ka = 1.3 ✕ 10−5) with 0.140 M NaOH. Calculate the pH of the result
Murljashka [212]

Answer:

(a) 2.7

(b) 4.44

(c) 4.886

(d) 5.363

(e) 5.570

(f)  12.30

Explanation:

Here we have the titration of a weak acid with the strong base NaOH. So in part (a) simply calculate the pH of a weak acid ; in the other parts we have to consider that a buffer solution will be present after some of the weak acid reacts completely the strong base producing the conjugate base. We may even arrive to the situation in which all of the acid will be just consumed and have only  the weak base present in the solution treating it as the pOH and the pH = 14 -pOH. There is also the possibility that all of the weak base will be consumed and then the NaOH will drive the pH.

Lets call HA propanoic acid and A⁻ its conjugate base,

(a) pH = -log √ (HA) Ka =-log √(0.28 x 1.3 x 10⁻⁵) = 2.7

(b) moles reacted HA = 50 x 10⁻³ L x 0.14 mol/L = 0.007 mol

mol left HA = 0.28 - 0.007 = 0.021

mol A⁻ produced = 0.007

Using the Hasselbalch-Henderson equation for buffer solutions:

pH = pKa + log ((A⁻/)/(HA)) = -log (1.3 x 10⁻⁵) + log (0.007/0.021)= 4.89 + (-0.48) = 4.44

(c) = mol HA reacted = 0.100 L x 0.14 mol/L = 0.014 mol

mol HA left = 0.028 -0.014 = 0.014 mol

mol A⁻ produced = 0.014

pH = -log (1.3 x 10⁻⁵) + log (0.014/0.014) =  4.886

(d) mol HA reacted = 150 x 10⁻³ L  x  x 0.14 mol/L = 0.021 mol

mol HA left = 0.028 - 0.021 = 0.007

mol A⁻ produced = 0.021

pH = -log (1.3 x 10⁻⁵) + log (0.021/0.007) =  5.363

(e) mol HA reacted = 200 x 10⁻³ L x 0.14 mol/L = 0.028 mol

mol HA left = 0

Now we only a weak base present and its pH is given by:

pH  = √(kb x (A⁻)  where Kb= Kw/Ka

Notice that here we will have to calculate the concentration of A⁻ because we have dilution effects the moment we added to the 100 mL of HA,  200 mL of NaOH 0.14 M. (we did not need to concern ourselves before with this since the volumes cancelled each other in the previous formulas)

mol A⁻ = 0.028 mOl

Vol solution = 100 mL + 200 mL = 300 mL

(A⁻) = 0.028 mol /0.3 L = 0.0093 M

and we also need to calculate the Kb for the weak base:

Kw = 10⁻¹⁴ = ka Kb ⇒   Kb = 10⁻¹⁴/1.3x 10⁻⁵ = 7.7 x 10⁻ ¹⁰

pH = -log (√( 7.7 x 10⁻ ¹⁰ x 0.0093) = 5.570

(f) Treat this part as a calculation of the pH of a strong base

moles of OH = 0.250 L x 0.14 mol = 0.0350 mol

mol OH remaining = 0.035 mol - 0.028 reacted with HA

= 0.007 mol

(OH⁻) = 0.007 mol / 0.350 L = 2.00 x 10 ⁻²

pOH = - log (2.00 x 10⁻²) = 1.70

pH = 14 - 1.70 = 12.30

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Hey there!:

Concentration of NaOH = 0.200 M

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