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Gnesinka [82]
3 years ago
12

What must be the molarity of an aqueous solution of trimethylamine, (ch3)3n, if it has a ph = 11.20? (ch3)3n+h2o⇌(ch3)3nh++oh−kb

=6.3×10−5?
Chemistry
1 answer:
Stolb23 [73]3 years ago
8 0

0.040 mol / dm³. (2 sig. fig.)

<h3>Explanation</h3>

(\text{CH}_3)_3\text{N} in this question acts as a weak base. As seen in the equation in the question, (\text{CH}_3)_3\text{N} produces \text{OH}^{-} rather than \text{H}^{+} when it dissolves in water. The concentration of \text{OH}^{-} will likely be more useful than that of \text{H}^{+} for the calculations here.

Finding the value of [\text{OH}^{-}] from pH:

Assume that \text{pK}_w = 14,

\begin{array}{ll}\text{pOH} = \text{pK}_w - \text{pH} \\ \phantom{\text{pOH}} = 14 - 11.20 &\text{True only under room temperature where }\text{pK}_w = 14 \\\phantom{\text{pOH}}= 2.80\end{array}.

[\text{OH}^{-}] =10^{-\text{pOH}} =10^{-2.80} = 1.59\;\text{mol}\cdot\text{dm}^{-3}.

Solve for [(\text{CH}_3)_3\text{N}]_\text{initial}:

\dfrac{[\text{OH}^{-}]_\text{equilibrium}\cdot[(\text{CH}_3)_3\text{NH}^{+}]_\text{equilibrium}}{[(\text{CH}_3)_3\text{N}]_\text{equilibrium}} = \text{K}_b = 1.58\times 10^{-3}

Note that water isn't part of this expression.

The value of Kb is quite small. The change in (\text{CH}_3)_3\text{N} is nearly negligible once it dissolves. In other words,

[(\text{CH}_3)_3\text{N}]_\text{initial} = [(\text{CH}_3)_3\text{N}]_\text{final}.

Also, for each mole of \text{OH}^{-} produced, one mole of (\text{CH}_3)_3\text{NH}^{+} was also produced. The solution started with a small amount of either species. As a result,

[(\text{CH}_3)_3\text{NH}^{+}] = [\text{OH}^{-}] = 10^{-2.80} = 1.58\times 10^{-3}\;\text{mol}\cdot\text{dm}^{-3}.

\dfrac{[\text{OH}^{-}]_\text{equilibrium}\cdot[(\text{CH}_3)_3\text{NH}^{+}]_\text{equilibrium}}{[(\text{CH}_3)_3\text{N}]_\textbf{initial}} = \text{K}_b = 1.58\times 10^{-3},

[(\text{CH}_3)_3\text{N}]_\textbf{initial} =\dfrac{[\text{OH}^{-}]_\text{equilibrium}\cdot[(\text{CH}_3)_3\text{NH}^{+}]_\text{equilibrium}}{\text{K}_b},

[(\text{CH}_3)_3\text{N}]_\text{initial} =\dfrac{(1.58\times10^{-3})^{2}}{6.3\times10^{-5}} = 0.040\;\text{mol}\cdot\text{dm}^{-3}.

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Calculate the initial rate for the formation of C at 25 ∘C, if [A]=0.50M and [B]=0.075M.Express your answer to two significant f
N76 [4]

The question is incomplete, here is the complete question:

Calculate the initial rate for the formation of C at 25°C, if [A]=0.50 M and [B]=0.075 M. Express your answer to two significant figures and include the appropriate units.Consider the reaction

A + 2B ⇔ C

whose rate at 25°C was measured using three different sets of initial concentrations as listed in the following table:

The table is attached below as an image.

<u>Answer:</u> The initial rate for the formation of C at 25°C is 2.25\times 10^{-2}Ms^{-1}

<u>Explanation:</u>

Rate law is defined as the expression which expresses the rate of the reaction in terms of molar concentration of the reactants with each term raised to the power their stoichiometric coefficient of that reactant in the balanced chemical equation.

For the given chemical equation:

A+2B\rightleftharpoons C

Rate law expression for the reaction:

\text{Rate}=k[A]^a[B]^b

where,

a = order with respect to A

b = order with respect to B

  • Expression for rate law for first trial:

5.4\times 10^{-3}=k(0.30)^a(0.050)^b ....(1)

  • Expression for rate law for second trial:

1.1\times 10^{-2}=k(0.30)^a(0.100)^b ....(2)

  • Expression for rate law for third trial:

2.2\times 10^{-2}=k(0.50)^a(0.050)^b ....(3)

Dividing 2 by 1, we get:

\frac{1.1\times 10^{-2}}{5.4\times 10^{-3}}=\frac{(0.30)^a(1.00)^b}{(0.30)^a(0.050)^b}\\\\2=2^b\\b=1

Dividing 3 by 1, we get:

\frac{2.2\times 10^{-2}}{5.4\times 10^{-3}}=\frac{(0.50)^a(0.050)^b}{(0.30)^a(0.050)^b}\\\\4.07=2^a\\a=2

Thus, the rate law becomes:

\text{Rate}=k[A]^2[B]^1       ......(4)

Now, calculating the value of 'k' by using any expression.

Putting values in equation 1, we get:

5.4\times 10^{-3}=k[0.30]^2[0.050]^1\\\\k=1.2M^{-2}s^{-1}

Calculating the initial rate of formation of C by using equation 4, we get:

k=1.2M^{-2}s^{-1}

[A] = 0.50 M

[B] = 0.075 M

Putting values in equation 4, we get:

\text{Rate}=1.2\times (0.50)^2\times (0.075)^1\\\\\text{Rate}=2.25\times 10^{-2}Ms^{-1}

Hence, the initial rate for the formation of C at 25°C is 2.25\times 10^{-2}Ms^{-1}

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What is the mass of solute in a 500 mL solution of 0.200 M
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16.4 grams is the mass of solute in a 500 mL solution of 0.200 M .

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atomic mass of Na3PO4 = 164 grams/mole

volume of the solution = 500 ml or 0.5 litres

molarity of sodium phosphate solution = 0.200 M

The formula for molarity will be used here to know the mass dissolved in the given volume of the solution:

The formula is

molarity = \frac{number of moles of solute}{volume in litres}

    putting the values in the equation, we get

molarity x volume = number of moles

0.200 X 0.5= number of  moles

number of moles = 0.1 moles

Atomic mass x number of moles = mass

putting the values in the above equation

164 x 0.1 = 16.4 grams

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Answer:

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<u>Number of molecules for 55.93 \mathrm{kg} \text { of } \mathrm{NaHCO}_{3}</u>

\text { Firstly molar mass is calculated of } \mathrm{NaHCO}_{3}:

Atomic mass of Na + H + C + 3(O)  = 22.99 + 1.008 + 12.01 + 3 × 16.00 = 84.00 g/mol

\text { Number of molecules of } \mathrm{NaHCO}_{3} \text { in } 55.93 \text { kg are as follows: }

55.93 \times\left(10^{3} \mathrm{gm}\right) \times \frac{1 \mathrm{mol} \mathrm{NaHCO}_{3}}{84.00 \mathrm{gm} \mathrm{NaHCO}_{3}} \times\left(6.022 \times 10^{23} \mathrm{molecules} \text { i.e Avogadro number }\right)

=4.010 \times 10^{26} \text { molecules of } \mathrm{NaHCO}_{3} \text { present in } 55.93 \mathrm{kg} \text { of } \mathrm{NaHCO}_{3}

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= Atomic mass of 3(Na) + P + 4(O)

= 3(22.99) + 30.97 + 4(16.00) = 163.94 g/mol

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