A biochemist needs \(750 \mathrm{~mL}\) of an acetic acid-sodium acetate buffer with \(\mathrm{pH}\) 4.50. Solid sodium acetate \(\left(\mathrm{CH}_{3} \mathrm{COONa}\right)\) and glacial acetic acid \(\left(\mathrm{CH}_{3} \mathrm{COOH}\right)\) are available. Glacial acetic acid is \(99 \% \mathrm{CH}_{3} \mathrm{COOH}\) by mass and has a density of \(1.05 \mathrm{~g} / \mathrm{mL}\). If the buffer is to be \(0.15 \mathrm{M}\) in \(\mathrm{CH}_{3} \mathrm{COOH}\), how many grams of \(\mathrm{CH}_{3} \mathrm{COONa}\) and how many milliliters of glacial acetic acid must be used?

Short Answer

Expert verified
To prepare 750 mL of a pH 4.50 buffer with a 0.15 M acetic acid, use 8.24 grams of sodium acetate and 6.49 mL of glacial acetic acid.

Step by step solution

01

Using the Henderson-Hasselbalch equation

The Henderson-Hasselbalch equation is given as: \[ \mathrm{pH} = \mathrm{p}K_a + \log \frac{[\mathrm{A}^-]}{[\mathrm{HA}]} \] where \([\mathrm{A}^-]\) represents the concentration of the conjugate base (sodium acetate), \([\mathrm{HA}]\) represents the concentration of the weak acid (acetic acid) and 𝑝𝐾𝑎 is the acid dissociation constant of the weak acid. For acetic acid, the 𝑝𝐾𝑎 value is 4.74. Given the pH of the buffer (which is 4.50) and the concentration of acetic acid (0.15 M), we can calculate the concentration of sodium acetate needed as follows: \[ 4.50 = 4.74 + \log \frac{[\mathrm{CH}_3\mathrm{COONa}]}{0.15} \]
02

Solve for the concentration of sodium acetate

Rearrange the equation to solve for the concentration of sodium acetate: \[ \log \frac{[\mathrm{CH}_3\mathrm{COONa}]}{0.15} = 4.50 - 4.74 \] \[ \log [\mathrm{CH}_3\mathrm{COONa}] - \log(0.15) = -0.24 \] \[ [\mathrm{CH}_3\mathrm{COONa}] = 10^{-0.24} \times 0.15 \] Calculating the concentration of sodium acetate, we get: \[ [\mathrm{CH}_3\mathrm{COONa}] = 0.134 \mathrm{M} \]
03

Find the mass of sodium acetate needed

We know the concentration and the volume of the buffer solution, so we can find the moles and, subsequently, the mass of sodium acetate needed: \[ \mathrm{moles~of~sodium~acetate} = [\mathrm{CH}_3\mathrm{COONa}] \times \mathrm{volume~of~buffer} \] \[ \mathrm{moles~of~sodium~acetate} = 0.134 \mathrm{M} \times 0.750 \mathrm{L} = 0.1005 \mathrm{~mol} \] Next, we will find the mass using the molar mass of sodium acetate (82.03 g/mol): \[ \mathrm{mass~of~sodium~acetate} = \mathrm{moles~of~sodium~acetate} \times \mathrm{molar~mass~of~sodium~acetate} \] \[ \mathrm{mass~of~sodium~acetate} = 0.1005 \mathrm{~mol} \times 82.03 \frac{\mathrm{g}}{\mathrm{mol}} = 8.24 \mathrm{~g} \]
04

Calculate the volume of glacial acetic acid needed

We know the buffer is to be 0.15 M in acetic acid. Convert concentration to moles using the volume of the buffer: \[ \mathrm{moles~of~acetic~acid} = [\mathrm{CH}_3\mathrm{COOH}] \times \mathrm{volume~of~buffer} \] \[ \mathrm{moles~of~acetic~acid} = 0.15 \mathrm{M} \times 0.750 \mathrm{L} = 0.1125 \mathrm{~mol} \] Now, we will find the mass of acetic acid using the molar mass of acetic acid (60.05 g/mol): \[ \mathrm{mass~of~acetic~acid} = \mathrm{moles~of~acetic~acid} \times \mathrm{molar~mass~of~acetic~acid} \] \[ \mathrm{mass~of~acetic~acid} = 0.1125 \mathrm{~mol} \times 60.05 \frac{\mathrm{g}}{\mathrm{mol}} = 6.756 \mathrm{~g} \] Now, let's calculate the volume considering that glacial acetic acid has only 99% acetic acid by mass and density \(1.05 \frac{\mathrm{g}}{\mathrm{mL}}\): \[ \mathrm{mass~of~glacial~acetic~acid} = \frac{\mathrm{mass~of~acetic~acid}}{0.99} = \frac{6.756 \mathrm{~g}}{0.99} = 6.82 \mathrm{~g} \] \[ \mathrm{volume~of~glacial~acetic~acid} = \frac{\mathrm{mass~of~glacial~acetic~acid}}{\mathrm{density}}=\frac{6.82 \mathrm{~g}}{1.05 \frac{\mathrm{g}}{\mathrm{mL}}} = 6.49 \mathrm{~mL} \] In conclusion, to prepare 750 mL of a pH 4.50 buffer with a 0.15 M acetic acid, we must use 8.24 grams of sodium acetate and 6.49 mL of glacial acetic acid.

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Most popular questions from this chapter

A \(35.0-\mathrm{mL}\) sample of \(0.150 \mathrm{M}\) acetic acid \(\left(\mathrm{CH}_{3} \mathrm{COOH}\right)\) is titrated with \(0.150 \mathrm{M} \mathrm{NaOH}\) solution. Calculate the \(\mathrm{pH}\) after the following volumes of base have been added: (a) \(0 \mathrm{~mL},(\mathbf{b})\) \(17.5 \mathrm{~mL},(\mathrm{c}) 34.5 \mathrm{~mL},(\) d) \(35.0 \mathrm{~mL},\) (e) \(35.5 \mathrm{~mL},\) (f) \(50.0 \mathrm{~mL} .\)

(a) Will \(\mathrm{Ca}(\mathrm{OH})_{2}\) precipitate from solution if the \(\mathrm{pH}\) of a \(0.050 \mathrm{M}\) solution of \(\mathrm{CaCl}_{2}\) is adjusted to \(8.0 ?\) (b) Will \(\mathrm{Ag}_{2} \mathrm{SO}_{4}\) precipitate when \(100 \mathrm{~mL}\) of \(0.050 \mathrm{M} \mathrm{AgNO}_{3}\) is mixed with \(10 \mathrm{~mL}\) of \(5.0 \times 10^{-2} \mathrm{M} \mathrm{Na}_{2} \mathrm{SO}_{4}\) solution?

A 20.0-mL sample of \(0.200 \mathrm{M}\) HBr solution is titrated with \(0.200 \mathrm{M} \mathrm{NaOH}\) solution. Calculate the \(\mathrm{pH}\) of the solution after the following volumes of base have been added: (a) \(15.0 \mathrm{~mL}\) (b) \(19.9 \mathrm{~mL}\) (c) \(20.0 \mathrm{~mL},\) (d) \(20.1 \mathrm{~mL},\) (e) \(35.0 \mathrm{~mL}\)

Assume that \(30.0 \mathrm{~mL}\) of a \(0.10 \mathrm{M}\) solution of a weak base \(\mathrm{B}\) that accepts one proton is titrated with a \(0.10 \mathrm{M}\) solution of the monoprotic strong acid HX. (a) How many moles of \(\mathrm{HX}\) have been added at the equivalence point? (b) What is the predominant form of \(\mathrm{B}\) at the equivalence point? (c) What factor determines the \(\mathrm{pH}\) at the equivalence point? (d) Which indicator, phenolphthalein or methyl red, is likely to be the better choice for this titration?

A solution contains \(2.0 \times 10^{-4} \mathrm{MAg}^{+}\) and \(1.5 \times 10^{-3} \mathrm{M}\) \(\mathrm{Pb}^{2+}\). If NaI is added, will AgI \(\left(K_{s p}=8.3 \times 10^{-17}\right)\) or \(\mathrm{PbI}_{2}\) \(\left(K_{s p}=7.9 \times 10^{-9}\right)\) precipitate first? Specify the concentration of \(1^{-}\) needed to begin precipitation.

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