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nignag [31]
3 years ago
11

When a diprotic acid is titrated with a strong base, and the Ka1 and Ka2 are significantly different, then the pH vs. volume plo

t of the titration will have Group of answer choices

Chemistry
1 answer:
dezoksy [38]3 years ago
4 0

Complete question is;

When a diprotic acid is titrated with a strong base, and the Ka1 and Ka2 are significantly different, then the pH vs. volume plot of the titration will have

a. a pH of 7 at the equivalence point.

b. two equivalence points below 7.

c. no equivalence point.

d. one equivalence point.

e. two distinct equivalence points

Answer:

Option E - Two Distinct Equivalence points

Explanation:

I've attached a sample diprotic acid titration curve.

In diprotic acids, the titration curves assists us to calculate the Ka1 and Ka2 of the acid. Thus, the pH at the half - first equivalence point in the titration will be equal to the pKa1 of the acid while the pH at the half - second equivalence point in a titration is equal to the pKa2 of the acid.

Thus, it is clear that there are two distinct equivalence points.

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mass of X extracted from the aqueous solution by 50 cm³ of ethoxy ethane = 3.33 g

Explanation:

The partition coefficient of X between ethoxy ethane (ether) and water, K is given by the formula

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Concentration of X in ether = (m/0.05) g/dm³

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Concentration of X in water = (5 - m/1) g/dm³

Using K = concentration of X in ether/concentration of X in water;

40 = (m/0.05)/(5 - m)

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In atmospheric chemistry, the following chemical reaction converts SO2, the predominant oxide of sulfur that comes from combusti
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Answer:

Explanation:

From the given information;

The chemical reaction can be well presented as follows:

\mathtt{SO_{2(g)} + \dfrac{1}{2}O_{2(g)} }  ⇄ \mathtt{3SO_{2(l)}}

Now, K is known to be the equilibrium constant and it can be represented in terms of each constituent activity:

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However, since we are dealing with liquids solutions;

K = \dfrac{1}{\dfrac{Pso_2}{P^0}\Big ( \dfrac{Po_2}{P^0} \Big)^{1/2}}   since the activity of a_{so_3} is equivalent to 1

Hence, under standard conditions(i.e at a pressure of 1 bar)

K = \dfrac{1}{Pso_2Po_2^{1/2}}

(b)

From the CRC Handbook, we are meant to determine the value of the Gibb free energy by applying the formula:

\Delta _{rxn} G^o = \sum \Delta_f \ G^o (products) - \sum \Delta_fG^o (reactants) \\ \\ = (1) (-368 \ kJ/mol) - (\dfrac{1}{2}) (0) - ((1) (-300.13 \ kJ/mol)) \\ \\ = -368 \ kJ/mol + 300.13 \ kJ/mol \\ \\  \simeq -68 \ kJ/mol

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(c)

Le's recall that:

At equilibrium, the instantaneous free energy is usually zero &

Q(reaction quotient) is equivalent to K(equilibrium constant)

So;

\mathtt{\Delta _{rxn} G = \Delta _{rxn} G^o + RT In Q}

\mathtt{0- \Delta _{rxn} G^o = RTIn K } \\ \\ \mathtt{ \Delta _{rxn} G^o = -RTIn K }  \\ \\  K = e^{\dfrac{\Delta_{rxn} G^o}{RT}} \\ \\  K = e^{^{\dfrac{67900 \ J/mol}{8.314 \ J/mol \times 298 \ K}} }

K =7.98390356\times 10^{11} \\ \\  \mathbf{K = 7.98 \times 10^{11}}

(d)

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This is because;

If  Q < K, then the reaction will proceed in the right direction towards the products.

However, if Q > K , then the reaction goes to the left direction. i.e to the reactants.

So;

Q= \dfrac{1}{Pso_2Po_2^{1/2}}

Since we are dealing with liquids;

Q= \dfrac{1}{1 \times 1^{1/2}}

Q = 1

Since Q < K; Then, the reaction proceeds in the right direction.

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