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Amiraneli [1.4K]
1 year ago
5

Ammonia has a Kb of 1.8 × 10−5. Find [H3O+], [OH−], pH, and pOH for a 0.310 M ammonia solution.

Chemistry
1 answer:
lawyer [7]1 year ago
5 0

Answer:

[H₃O⁺] = 4.3 × 10⁻¹² mol·L⁻¹; [OH⁻] = 2.4 × 10⁻³ mol·L⁻¹;

pH = 11.4; pOH = 2.6

Explanation:

The chemical equation is

\rm NH$_{3}$ + \text{H}$_{2}$O \, \rightleftharpoons \,$ NH$_{4}^{+}$ + \,\text{OH}$^{-}$

For simplicity, let's re-write this as

\rm B + H$_{2}$O \, \rightleftharpoons\,$ BH$^{+}$ + OH$^{-}$

1. Calculate [OH]⁻

(a) Set up an ICE table.  

   B + H₂O ⇌ BH⁺ + OH⁻

0.310               0        0

   -x                  +x      +x

0.310-x               x        x

K_{\text{b}} = \dfrac{\text{[BH}^{+}]\text{[OH}^{-}]}{\text{[B]}} = 1.8 \times 10^{-5}\\\\\dfrac{x^{2}}{0.100 - x} = 1.8 \times 10^{-5}

Check for negligibility:

\dfrac{0.310}{1.8 \times 10^{-5}} = 17 000 > 400\\\\x \ll 0.310

(b) Solve for [OH⁻]

\dfrac{x^{2}}{0.310} = 1.8 \times 10^{-5}\\\\x^{2} = 0.310 \times 1.8 \times 10^{-5}\\x^{2} = 5.58 \times 10^{-6}\\x = \sqrt{5.58 \times 10^{-6}}\\x = \text{[OH]}^{-} = \mathbf{2.4 \times 10^{-3}} \textbf{ mol/L}

2. Calculate the pOH

\text{pOH} = -\log \text{[OH}^{-}] = -\log(2.4 \times 10^{-3}) = \mathbf{2.6}

3. Calculate the pH

\text{pH} = 14.00 - \text{pOH} = 14.00 - 2.6 = \mathbf{11.4}

4 Calculate [H₃O⁺]

\text{H$_{3}$O$^{+}$} = 10^{-\text{pH}} = 10^{-11.4} = \mathbf{4.2 \times 10^{-12}} \textbf{ mol/L}

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Answer

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Explanation:

We can go about this using the percentage compositions.

First, we calculate the percentage composition of the copper sulphate. This is obtainable by using the mass.

0.96/1.5 * 100 = 64%

Hence the percentage by mass of the water present is 36%

The molar mass of the anhydrous sulphate is 64 + 32 +4(16) = 160g/mol

The molar mass of the water is 2(1) + 16 = 18g/mol

Not forgetting that it is in multiples of x, the total molar mass of the water is 18x moles

The total mass of the copper sulphate hydrate is 160+ 18x

Now how do we get x? Like it is said earlier, the percentage composition is constant.

Hence, 64/100 * (160 + 18x) = 160

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16000 = 10,240 + 1152x

16,000 - 10,240 = 1152x

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x = 5760/1152

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7 0
2 years ago
A 15.0 mL sample of 0.013 M HNO3 is titrated with 0.017 M CH$NH2 which he Kb=3.9 X 10-10. Determine the pH at these points: At t
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<u>Answer:</u> The pH of the solution in the beginning is 1.89 and the pH of the solution after the addition of base is

<u>Explanation:</u>

  • <u>For 1:</u> At the beginning

To calculate the pH of the solution, we use the equation:

pH=-\log[H^+]

We are given:

Nitric acid is a monoprotic acid and it dissociates 1 mole of hydrogen ions. So, the concentration of hydrogen ions is 0.013 M

[H^+]=0.013M

Putting values in above equation, we get:

pH=-\log(0.013)\\\\pH=1.89

  • <u>For 2:</u>

To calculate the number of moles, we use the equation:  

\text{Molarity of the solution}=\frac{\text{Moles of solute}\times 1000}{\text{Volume of solution (in mL)}}

  • <u>For nitric acid:</u>

Molarity of nitric acid solution = 0.013 M

Volume of solution = 15 mL

Putting values in above equation, we get:

0.013M=\frac{\text{Moles of }HNO_3\times 1000}{15}\\\\\text{Moles of }HNO_3=1.95\times 10^{-4}mol

  • <u>For methylamine:</u>

Molarity of methylamine solution = 0.017 M

Volume of solution = 10 mL

Putting values in above equation, we get:

0.017M=\frac{\text{Moles of }CH_3NH_2\times 1000}{10}\\\\\text{Moles of }CH_3NH_2=1.7\times 10^{-4}mol

  • The chemical equation for the reaction of nitric acid and methylamine follows:

                       HNO_3+CH_3NH_2\rightarrow CH_3NH_3^++NO_3^-

As, the mole ratio of nitric acid and methyl amine is 1 : 1. So, the limiting reagent will be the reactant whose number of moles are less, which is methyl amine.

By Stoichiometry of the reaction:

1 mole of methyl amine produces 1 mole of CH_3NH_3^+

So, 1.7\times 10^{-4}mol of methyl amine will produce = \frac{1}{1}\times 1.7\times 10^{-4}=1.7\times 10^{-4}\text{ moles of }CH_3NH_3^+

To calculate the pK_b of base, we use the equation:

pK_b=-\log(K_b)

where,

K_b = base dissociation constant = 3.9\times 10^{-10}

Putting values in above equation, we get:

pK_b=-\log(3.9\time 10^{-10})\\\\pK_b=9.41

  • To calculate the pOH of basic buffer, we use the equation given by Henderson Hasselbalch:

pOH=pK_b+\log(\frac{[salt]}{[base]})

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We are given:

pK_b=9.41

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Putting values in above equation, we get:

pOH=9.41+\log(\frac{6.8\times 10^{-6}}{6.8\times 10^{-6}})\\\\pOH=9.41

To calculate pH of the solution, we use the equation:

pH+pOH=14\\pH=14-9.41=4.59

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After this precipitate has been filtered off and the pH is adjusted to 8, addition of H2S and (NH4)2HPO4 does not lead to the formation of any other precipitate.

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