At 298 K, a certain buffer solution contains equal concentrations of $X^{-}$ and $HX$. $K_b$ for $X^-$ is $10^{-10}$. What is the pH of this buffer solution ?
The problem asks for the pH of a buffer solution containing equal concentrations of a weak acid ($HX$) and its conjugate base ($X^-$). We are given the base dissociation constant ($K_b$) for the conjugate base $X^-$.
A buffer solution maintains a relatively stable pH. When the concentrations of the weak acid ($HX$) and its conjugate base ($X^-$) are equal, the pH of the buffer solution is equal to the $pK_a$ of the weak acid.
The Henderson-Hasselbalch equation describes the pH of a buffer:
$pH = pK_a + \log \frac{[X^{-}]}{[HX]}$In this specific case, $[X^{-}] = [HX]$, so the ratio $\frac{[X^{-}]}{[HX]} = 1$. The equation simplifies to:
$pH = pK_a + \log(1)$ $pH = pK_a + 0$ $pH = pK_a$We need to find the $pK_a$ of the weak acid $HX$. We are given $K_b$ for the conjugate base $X^-$, which is $10^{-10}$. We know the relationship between the acid dissociation constant ($K_a$), the base dissociation constant ($K_b$), and the ion product of water ($K_w$):
$K_a \times K_b = K_w$At 298 K, $K_w = 1.0 \times 10^{-14}$. We can find $K_a$:
$K_a = \frac{K_w}{K_b} = \frac{1.0 \times 10^{-14}}{10^{-10}}$ $K_a = 1.0 \times 10^{-4}$Now, we calculate $pK_a$:
$pK_a = -\log(K_a)$ $pK_a = -\log(1.0 \times 10^{-4})$ $pK_a = -(-4)$ $pK_a = 4$Since $pH = pK_a$ when the concentrations of the acid and its conjugate base are equal:
$pH = 4$Therefore, the pH of the buffer solution is 4.
For a certain reaction R $\rightarrow$ Product, the plot of [R] vs time has a negative slope as shown. The order of reaction is :

| List I (Order of reaction) | List II (Unit of rate constant) |
| A. Zero order | I. $mol^{-1} L s^{-1}$ |
| B. First order | II. $mol^{-2} L^2 s^{-1}$ |
| C. Second order | III. $s^{-1}$ |
| D. Third order | IV. $mol L^{-1} s^{-1}$ |
Calculate emf of the half cell given below :
$$Pt(s) | H_2 (g, 2 \text{ atm}) | HCl (aq, 0.02 \text{ M})$$
$$E_{H_2 /H^+}^\circ = 0 \text{ V}$$
(Given : $\frac{2.303 RT}{F} = 0.059$, $\log 2 = 0.3010$)