We begin with the more accurate expression for the dissociation of a weak acid:
$$ K_a = \frac{Cx^2}{1 - x} $$ where $ C $ is the initial concentration of the acid, and $ x $ is the degree of dissociation.
The hydrogen ion concentration is given by:
$$ [H^+] = Cx $$ So, $$ pH = -\log(Cx) $$
Similarly, the $ pK_a $ is defined as:
$$ pK_a = -\log(K_a) = -\log\left(\frac{Cx^2}{1 - x}\right) $$
Now, we calculate $ pH - pK_a $:
$$ pH - pK_a = -\log(Cx) + \log\left(\frac{Cx^2}{1 - x}\right) = \log\left(\frac{Cx^2}{Cx(1 - x)}\right) = \log\left(\frac{x}{1 - x}\right) $$
This gives us the general relation:
$$ pH - pK_a = \log\left(\frac{x}{1 - x}\right) $$
If $ pH = pK_a $, then:
$$ \log\left(\frac{x}{1 - x}\right) = 0 \Rightarrow \frac{x}{1 - x} = 1 \Rightarrow x = 1 - x \Rightarrow 2x = 1 \Rightarrow x = \frac{1}{2} $$
Thus, when the degree of dissociation $ x = 0.5 $, the pH equals the $ pK_a $, which corresponds to the midpoint of the titration curve.
Final Answer:
The correct expression for $ pH - pK_a $ without approximation is:
$$ \ \log\left(\frac{x}{1 - x}\right) $$
A substance 'X' (1.5 g) dissolved in 150 g of a solvent 'Y' (molar mass = 300 g mol$^{-1}$) led to an elevation of the boiling point by 0.5 K. The relative lowering in the vapour pressure of the solvent 'Y' is $____________ \(\times 10^{-2}\). (nearest integer)
[Given : $K_{b}$ of the solvent = 5.0 K kg mol$^{-1}$]
Assume the solution to be dilute and no association or dissociation of X takes place in solution.
Inductance of a coil with \(10^4\) turns is \(10\,\text{mH}\) and it is connected to a DC source of \(10\,\text{V}\) with internal resistance \(10\,\Omega\). The energy density in the inductor when the current reaches \( \left(\frac{1}{e}\right) \) of its maximum value is \[ \alpha \pi \times \frac{1}{e^2}\ \text{J m}^{-3}. \] The value of \( \alpha \) is _________.
\[ (\mu_0 = 4\pi \times 10^{-7}\ \text{TmA}^{-1}) \]