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The degree of dissociation of weak elect...

The degree of dissociation of weak electrolyde is inversely proportional to the square root fo concentration. It is called Ostwald's dilution law.
`alpha = sqrt((K_(a))/(c))` As the tempertaure increases, degree of dissociation will increase.
`(alpha_(1))/(alpha_(2)) = sqrt((K_(a_(1)))/(K_(a_(2))))` if concentration is same.
`(alpha_(1))/(alpha_(2)) = sqrt((c_(2))/(c_(1)))` if acid is same.
`pH` of `0.005 M HCOOH [K_(a) = 2 xx 10^(-4)]` is equal to

A

`3`

B

`2`

C

`4`

D

`5`

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To find the pH of a 0.005 M solution of formic acid (HCOOH) with a dissociation constant \( K_a = 2 \times 10^{-4} \), we can follow these steps: ### Step 1: Write the dissociation equation The dissociation of formic acid in water can be represented as: \[ \text{HCOOH} \rightleftharpoons \text{HCOO}^- + \text{H}_3\text{O}^+ \] ### Step 2: Set up the expression for the dissociation constant \( K_a \) The expression for the dissociation constant \( K_a \) is given by: \[ K_a = \frac{[\text{HCOO}^-][\text{H}_3\text{O}^+]}{[\text{HCOOH}]} \] ### Step 3: Define the initial concentrations and changes Let the degree of dissociation be \( \alpha \). Initially, the concentration of HCOOH is 0.005 M. At equilibrium: - The concentration of HCOOH will be \( 0.005(1 - \alpha) \) - The concentration of HCOO⁻ and H₃O⁺ will both be \( 0.005\alpha \) ### Step 4: Substitute into the \( K_a \) expression Substituting the equilibrium concentrations into the \( K_a \) expression: \[ K_a = \frac{(0.005\alpha)(0.005\alpha)}{0.005(1 - \alpha)} = \frac{0.005^2 \alpha^2}{0.005(1 - \alpha)} \] This simplifies to: \[ K_a = \frac{0.005\alpha^2}{1 - \alpha} \] ### Step 5: Substitute the value of \( K_a \) Now substitute \( K_a = 2 \times 10^{-4} \): \[ 2 \times 10^{-4} = \frac{0.005\alpha^2}{1 - \alpha} \] ### Step 6: Rearranging the equation Multiplying both sides by \( (1 - \alpha) \): \[ 2 \times 10^{-4} (1 - \alpha) = 0.005\alpha^2 \] Expanding this gives: \[ 2 \times 10^{-4} - 2 \times 10^{-4} \alpha = 0.005\alpha^2 \] Rearranging leads to: \[ 0.005\alpha^2 + 2 \times 10^{-4} \alpha - 2 \times 10^{-4} = 0 \] ### Step 7: Solve the quadratic equation Using the quadratic formula \( \alpha = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a} \): - Here, \( a = 0.005 \), \( b = 2 \times 10^{-4} \), and \( c = -2 \times 10^{-4} \). Calculating the discriminant: \[ b^2 - 4ac = (2 \times 10^{-4})^2 - 4(0.005)(-2 \times 10^{-4}) = 4 \times 10^{-8} + 0.00004 = 4.04 \times 10^{-8} \] Now substituting into the quadratic formula: \[ \alpha = \frac{-2 \times 10^{-4} \pm \sqrt{4.04 \times 10^{-8}}}{2 \times 0.005} \] Calculating the square root: \[ \sqrt{4.04 \times 10^{-8}} \approx 2.01 \times 10^{-4} \] Thus: \[ \alpha = \frac{-2 \times 10^{-4} + 2.01 \times 10^{-4}}{0.01} \approx 0.181 \] ### Step 8: Calculate \([H_3O^+]\) The concentration of \( [H_3O^+] \) is: \[ [H_3O^+] = 0.005\alpha = 0.005 \times 0.181 \approx 9.05 \times 10^{-4} \text{ M} \] ### Step 9: Calculate the pH Using the formula for pH: \[ \text{pH} = -\log[H_3O^+] = -\log(9.05 \times 10^{-4}) \] Using logarithmic properties: \[ \text{pH} = -\log(9.05) - \log(10^{-4}) \approx -0.956 + 4 \approx 3.044 \] Thus, the pH is approximately 3. ### Final Answer The pH of the 0.005 M HCOOH solution is approximately **3**.

To find the pH of a 0.005 M solution of formic acid (HCOOH) with a dissociation constant \( K_a = 2 \times 10^{-4} \), we can follow these steps: ### Step 1: Write the dissociation equation The dissociation of formic acid in water can be represented as: \[ \text{HCOOH} \rightleftharpoons \text{HCOO}^- + \text{H}_3\text{O}^+ \] ...
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The degree of dissociation of weak electrolyde is inversely proportional to the square root fo concentration. It is called Ostwald's dilution law. alpha = sqrt((K_(a))/(c)) As the tempertaure increases, degree of dissociation will increase. (alpha_(1))/(alpha_(2)) = sqrt((K_(a_(1)))/(K_(a_(2)))) if concentration is same. (alpha_(1))/(alpha_(2)) = sqrt((c_(2))/(c_(1))) if acid is same. a_(1) and a_(2) are in ratio of 1:2, K_(a_(1)) = 2xx10^(-4) . What will be K_(a_(2)) ?

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