Two drops of indicator \(\operatorname{HIn}\left(K_{\mathrm{a}}=1.0 \times 10^{-9}\right)\), where \(\mathrm{HIn}\) is yellow and \(\mathrm{In}^{-}\) is blue, are placed in \(100.0 \mathrm{~mL}\) of \(0.10 \mathrm{M} \mathrm{HCl}\). a. What color is the solution initially? b. The solution is titrated with \(0.10 \mathrm{M} \mathrm{NaOH}\). At what \(\mathrm{pH}\) will the color change (yellow to greenish yellow) occur? c. What color will the solution be after \(200.0 \mathrm{~mL} \mathrm{NaOH}\) has been added?

Short Answer

Expert verified
The initial color of the solution is yellow. The color change will occur at pH = 9. The final color of the solution will be blue.

Step by step solution

01

Determine initial color of the solution

Since we have \(\mathrm{HIn}\) in \(0.10 \mathrm{M} \mathrm{HCl}\) solution, the strong acid will protonate the indicator, making being in the acid form. The acid form of the indicator (HIn) is yellow. Therefore, the initial color of the solution will be yellow. Answer (a): The initial color of the solution is yellow.
02

Calculate the pH at which the color change occurs

The color change occurs when the weak acid and its conjugate base are in equal proportion. The Henderson-Hasselbalch equation relates the \(\mathrm{pH}\), \(\mathrm{p}K_{\mathrm{a}}\), and the ratio of concentrations of the conjugate base to weak acid as follows: \[\mathrm{pH} = \mathrm{p}K_{\mathrm{a}} + \log \frac{[\mathrm{In}^{-}]}{[\mathrm{HIn}]}\] We need to find the \(\mathrm{pH}\) value when \([\mathrm{In}^{-}] = [\mathrm{HIn}]\). In this case: \[\mathrm{pH} = \mathrm{p}K_{\mathrm{a}} + \log \frac{[\mathrm{In}^{-}]}{[\mathrm{HIn}]} = \mathrm{p}K_{\mathrm{a}} + \log(1) = \mathrm{p}K_{\mathrm{a}}\] Now, calculate the \(\mathrm{p}K_{\mathrm{a}}\) value: \[\mathrm{p}K_{\mathrm{a}} = -\log(K_{\mathrm{a}}) = -\log(1.0 \times 10^{-9}) = 9\] Answer (b): The color change will occur at \(\mathrm{pH} = 9\).
03

Determine the final color after adding 200.0 mL of 0.10 M NaOH

To find the final color, we can calculate the final pH of the solution after adding 200.0 mL of 0.10 M \(\mathrm{NaOH}\) to 100.0 mL of 0.10 M \(\mathrm{HCl}\). Using the stoichiometry of the reaction, moles of \(\mathrm{HCl}\) can be calculated as: moles of \(\mathrm{HCl}\) = molarity × volume = 0.10 \(\mathrm{mol/L} \) × 0.100 \(\mathrm{L} \) = 0.010 \(\mathrm{mol} \) moles of \(\mathrm{NaOH}\) = 0.10 \(\mathrm{mol/L} \) × 0.200 \(\mathrm{L} \) = 0.020 \(\mathrm{mol} \) Since the moles of \(\mathrm{NaOH}\) are greater than the moles of \(\mathrm{HCl}\), the solution is now a basic solution (the excess OH- ions will remain in the solution). After the reaction between \(\mathrm{NaOH}\) and \(\mathrm{HCl}\), there will still be some \(\mathrm{NaOH}\) left: moles of excess \(\mathrm{NaOH}\) = moles of \(\mathrm{NaOH}\) - moles of \(\mathrm{HCl}\) = 0.020 \(\mathrm{mol} \) - 0.010 \(\mathrm{mol} \) = 0.010 \(\mathrm{mol} \) Now, calculate the final concentration of excess \(\mathrm{NaOH}\): \[ [\mathrm{OH}^-] = \frac{0.010 \, \mathrm{mol}}{0.100 \, \mathrm{L}+0.200 \, \mathrm{L}} = 0.0333 \, \mathrm{M} \] Now, calculate the \(\mathrm{pOH}\) and \(\mathrm{pH}\): \[\mathrm{pOH} = -\log({[\mathrm{OH}^-]}) = -\log(0.0333) = 1.48\] \[\mathrm{pH} = 14 - \mathrm{pOH} = 14 - 1.48 = 12.52\] Since the final pH is greater than 9 (the pH at which the color change occurs), the indicator will be present predominantly in its conjugate base form (In-), which is blue. Answer (c): The final color of the solution will be blue.

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Most popular questions from this chapter

Malonic acid \(\left(\mathrm{HO}_{2} \mathrm{CCH}_{2} \mathrm{CO}_{2} \mathrm{H}\right)\) is a diprotic acid. In the titration of malonic acid with \(\mathrm{NaOH}\), stoichiometric points occur at \(\mathrm{pH}=3.9\) and \(8.8\). A \(25.00-\mathrm{mL}\) sample of malonic acid of unknown concentration is titrated with \(0.0984 \mathrm{M} \mathrm{NaOH}\), requiring \(31.50 \mathrm{~mL}\) of the \(\mathrm{NaOH}\) solution to reach the phenolphthalein end point. Calculate the concentration of the initial malonic acid solution. (See Exercise 113.)

Could a buffered solution be made by mixing aqueous solutions of \(\mathrm{HCl}\) and \(\mathrm{NaOH}\) ? Explain. Why isn't a mixture of a strong acid and its conjugate base considered a buffered solution?

A buffer is made using \(45.0 \mathrm{~mL}\) of \(0.750 \mathrm{M} \mathrm{HC}_{3} \mathrm{H}_{5} \mathrm{O}_{2}\left(K_{\mathrm{a}}=\right.\) \(1.3 \times 10^{-5}\) ) and \(55.0 \mathrm{~mL}\) of \(0.700 \mathrm{M} \mathrm{NaC}_{3} \mathrm{H}_{5} \mathrm{O}_{2}\). What volume of \(0.10 M\) NaOH must be added to change the \(\mathrm{pH}\) of the original buffer solution by \(2.5 \% ?\)

Calculate the \(\mathrm{pH}\) of a solution that is \(0.40 \mathrm{M} \mathrm{H}_{2} \mathrm{NNH}_{2}\) and \(0.80 \mathrm{M} \mathrm{H}_{2} \mathrm{NNH}_{3} \mathrm{NO}_{3} .\) In order for this buffer to have \(\mathrm{pH}=\) \(\mathrm{p} K_{\mathrm{a}}\), would you add \(\mathrm{HCl}\) or \(\mathrm{NaOH}\) ? What quantity (moles) of which reagent would you add to \(1.0 \mathrm{~L}\) of the original buffer so that the resulting solution has \(\mathrm{pH}=\mathrm{p} K_{\mathrm{a}}\) ?

Calculate the ratio \(\left[\mathrm{NH}_{3}\right] /\left[\mathrm{NH}_{4}{ }^{+}\right]\) in ammonia/ammonium chloride buffered solutions with the following \(\mathrm{pH}\) values: a. \(\mathrm{pH}=9.00\) b. \(\mathrm{pH}=8.80\) c. \(\mathrm{pH}=10.00\) d. \(\mathrm{pH}=9.60\)

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