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Ionic Equilibrium question

2020 · 5 Sep · Shift 1 · Q14
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  5. /2020 · 5 Sep · Shift 1 · Q14

Ionic Equilibrium question

2020 · 5 Sep · Shift 1 · Q14

JEE MainChemistryIonic EquilibriumNumerical+4 / −1
A soft drink was bottled with a partial pressure of CO2CO_2CO2​ of 3 bar over the liquid at room temperature. The partial pressure of CO2CO_2CO2​ over the solution approaches a value of 30 bar when 44 g of CO2CO_2CO2​ is dissolved in 1 kg of water at room temperature. The approximate pH of the soft drink is ‾×\underline{\hspace{2cm}}\times​× 10–1. (First dissociation constant of H2CO3H_2CO_3H2​CO3​ = 4.0 ×\times× 10–7; log 2 = 0.3; density of the soft drink = 1 g mL–1) .
Numerical answer
View written solutionFree

Correct answer: 37

  1. Use Henry’s law to find dissolved CO2CO_2CO2​ in the soft drink

At room temperature, we are told that when 44 g44\,\text{g}44g of CO2CO_2CO2​ is dissolved in 1 kg1\,\text{kg}1kg of water, the equilibrium partial pressure is 30 bar30\,\text{bar}30bar.

  • Moles of CO2CO_2CO2​ in 44 g44\,\text{g}44g: n=4444=1 moln = \frac{44}{44} = 1\,\text{mol}n=4444​=1mol

So, for this reference condition: nkg water=1 mol kg−1\frac{n}{\text{kg water}} = 1\,\text{mol kg}^{-1}kg watern​=1mol kg−1 corresponds to pCO2=30 barp_{CO_2} = 30\,\text{bar}pCO2​​=30bar

By Henry’s law, dissolved concentration is proportional to partial pressure.

For the soft drink bottled at 3 bar3\,\text{bar}3bar: dissolved CO2=1×330=0.1 mol kg−1\text{dissolved } CO_2 = 1\times \frac{3}{30} = 0.1\,\text{mol kg}^{-1}dissolved CO2​=1×303​=0.1mol kg−1

Since density of soft drink is 1 g mL−11\,\text{g mL}^{-1}1g mL−1, 1 kg1\,\text{kg}1kg solution is approximately 1 L1\,\text{L}1L. Hence we take C≈0.1 MC \approx 0.1\,\text{M}C≈0.1M for dissolved carbonic acid species.


  1. Treat dissolved CO2CO_2CO2​ as weak acid H2CO3H_2CO_3H2​CO3​

First dissociation: H2CO3⇌H++HCO3−H_2CO_3 \rightleftharpoons H^+ + HCO_3^-H2​CO3​⇌H++HCO3−​

Given: Ka=4.0×10−7K_a = 4.0\times 10^{-7}Ka​=4.0×10−7

Initial concentration: C=0.1 MC = 0.1\,\text{M}C=0.1M

Let dissociation be xxx:

  • [H+]=x[H^+] = x[H+]=x
  • [HCO3−]=x[HCO_3^-] = x[HCO3−​]=x
  • [H2CO3]=0.1−x≈0.1[H_2CO_3] = 0.1 - x \approx 0.1[H2​CO3​]=0.1−x≈0.1

Then Ka=x20.1K_a = \frac{x^2}{0.1}Ka​=0.1x2​

So, x2=4.0×10−7×0.1=4.0×10−8x^2 = 4.0\times 10^{-7}\times 0.1 = 4.0\times 10^{-8}x2=4.0×10−7×0.1=4.0×10−8

x=2×10−4 Mx = 2\times 10^{-4}\,\text{M}x=2×10−4M

Thus, [H+]=2×10−4[H^+] = 2\times 10^{-4}[H+]=2×10−4


  1. Calculate pH

pH=−log⁡(2×10−4)\text{pH} = -\log(2\times 10^{-4})pH=−log(2×10−4) =4−log⁡2= 4 - \log 2=4−log2 Given log⁡2=0.3\log 2 = 0.3log2=0.3, pH=4−0.3=3.7\text{pH} = 4 - 0.3 = 3.7pH=4−0.3=3.7


  1. Match with required format

The question asks for pH in the form: ‾×10−1\underline{\hspace{2cm}}\times 10^{-1}​×10−1

Since 3.7=37×10−13.7 = 37\times 10^{-1}3.7=37×10−1

the required integer is: 37\boxed{37}37​


  1. Comparison with stored answer

Stored correct answer = 373737

Our derived answer also = 373737.

So the answer agrees.

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