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geniusboy [140]

2 years ago

12

What is the molarity of a potassium triiodide solution, KI3(aq), if 30.00 mL of the solution is required to completely react wit

h 25.00 mL of a 0.500 M thiosulfate solution, K2S2O3(aq)

1 answer:

vfiekz [6]2 years ago

3 0

Answer:

The molarity is 0.203 M

Explanation:

Using the formula C(oxi) x V(oxi) / [C(red) x V(red)] = N(oxi) / N(red)

Where oxi and red means reducing agent and oxidising agent respectively.

C = Concentration, V = Volume and N = number of moles.

C(oxi) = 0.5 M

V(oxi) = mL

C(red) = ?

V(red) = 30mL

Equation of reaction = 2K2S2O3 + KI3 = K2S4O6 + 3KI

so N(red) = 1 , N(oxi) = 2

from the equation above,

C(red) = 0.5 x 25 x 1 / (2 x 30)

= 0.203 M.

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50.0 mL solution of 0.160 M potassium alaninate ( H 2 NC 2 H 5 CO 2 K ) is titrated with 0.160 M HCl . The p K a values for the

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a) 6.12

b) 1.87

Explanation:

At the onset of the equivalence point (i.e the first equivalence point); alaninate is being converted to alanine.

$H_2NC_2H_5CO^-_2$ $+$ $H^+$ ------> $H_3}^+NC_2H_5CO^-_2$

1 mole of alaninate react with 1 mole of acid to give 1 mole of alanine;

therefore 50.0 mL of 0.160 M alaninate required 50.0 mL of 0.160M HCl to reach the first equivalence point.

The concentration of alanine can be gotten via the following process as shown below;

$[H_3}^+NC_2H_5CO^-_2]$ = $\frac{initial moles of alaninate}{total volume}$

$[H_3}^+NC_2H_5CO^-_2]$ = $\frac{(50.0mL)*(0.160M)}{(50.0mL+50.0mL)}$

$[H_3}^+NC_2H_5CO^-_2]$ = $\frac{8}{100mL}$

$[H_3}^+NC_2H_5CO^-_2]$ = 0.08 M

Alanine serves as an intermediary form, however the concentration of $H^+$ and the pH can be determined as follows;

$[H^+]$ = $\sqrt{\frac{K_{a1}K_{a2}{[H_3}^+NC_2H_5CO^-_2]+K_{a1}K_w}{ K_{a1}{[H_3}^+NC_2H_5CO^-_2] } }$

$[H^+]$ = $\sqrt{\frac{ (10^{-pK_{a1})}(10^{-pK_{a2})}(0.08)+(10^{-pK_{a1})}(1.0*10^{-14})} {(10^{-pK_{a1}})+(0.08)} }$

$[H^+]$ = $\sqrt{\frac{ (10^{-2.344})(10^{-9.868})(0.08)+(10^{-2.344})(1.0*10^{-14})} {(10^{-2.344})+(0.08)} }$

$[H^+]$ = $7.63*10^{-7}M$

pH = - log $[H^+]$

pH = $-log[7.63*10^{-7}]$

pH= 6.12

Therefore, the pH of the first equivalent point = 6.12

b) At the second equivalence point; all alaninate is converted into protonated alanine.

$H_2NC_2H_5CO^-_2$ $+$ $H^+$ -----> $H^+_3NC_2H_5CO^-_2$

$H^+_3NC_2H_5CO^-_2$ $+$ $H^+$ -----> $H^+_3NC_2H_5CO_2H$

Here; we have a situation where 1 mole of alaninate react with 2 moles of acid to give 1 mole of protonated alanine;

Moreover, 50.0 mL of 0.160 M alaninate is needed to produce 100.0mL of 0.160 M HCl in order to achieve the second equivalence point.

Thus, the concentration of protonated alanine can be determined as:

$[H^+_3NC_2H_5CO_2H]$ = $\frac{initial moles of alaninate}{total volume}$

$[H^+_3NC_2H_5CO_2H]$ = $\frac{(50.0mL)*(0.160M)}{(50.0mL+100.0mL)}$

$[H^+_3NC_2H_5CO_2H]$ = $\frac{8}{150}$

$[H^+_3NC_2H_5CO_2H]$ = 0.053 M

The pH at the second equivalence point can be calculated via the dissociation of protonated alanine at equilibrium which is represented as:

$H^+_3NC_2H_5CO_2H$ ⇄ $H^+_3NC_2H_5CO^-_2$ $+$ $H^+$

(0.053 - x) x x

$K_{a1}$ = $\frac{[H^+] [H^+_3NC_2H_5CO^-_2]}{[H^+_3NC_2H_5CO_2H]}$

$10^{-PK_{a1}}$ = $\frac{x*x}{(0.053-x)}$

$10^{-2.344} =\frac{x^2}{(0.053-x)}$

$0.00453 = \frac{x^2}{(0.053-x)}$

$0.00453(0.053-x) =x^2$

$x^2+0.00453x-(2.4009*10^{-4})$

Using quadratic equation formula;

$\frac{-b+/-\sqrt{b^2-4ac} }{2a}$

we have:

$\frac{-0.00453+\sqrt{(0.00453)^2-4(1)(-2.4009*10^{-4})} }{2(1)}$ OR $\frac{-0.00453-\sqrt{(0.00453)^2-4(1)(-2.4009*10^{-4})} }{2(1)}$

= 0.0134 OR -0.0179

So; we go by the positive integer which says

x = 0.0134

So $[H^+]=[H_3^+NC_2H_5CO^-_2]= 0.0134 M$

pH = $-log[H^+]$

pH = $-log[0.0134]$

pH = 1.87

Thus, the pH of the second equivalent point = 1.87

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3 years ago