Step 1: Calculate the initial pH of the buffer solution.
Using the Henderson-Hasselbalch equation for a basic buffer: $$pOH_{initial} = pK_b + \log_{10} \frac{[salt]}{[base]} = 4.745 + \log_{10} \frac{0.10}{0.10} = 4.745$$ $$pH_{initial} = 14 - pOH_{initial} = 9.255$$
Step 2: Calculate the pH after the addition of HCl.
The reaction with HCl changes the concentrations of the base and its salt: $$NH_3 + HCl \rightarrow NH_4^+ + Cl^-$$ New moles: \( [NH_3] = 0.05 \) M, \( [NH_4^+] = 0.15 \) M $$pOH_{final} = pK_b + \log_{10} \frac{[NH_4^+]}{[NH_3]} = 4.745 + \log_{10} \frac{0.15}{0.05} = 4.745 + 0.477 = 5.222$$ $$pH_{final} = 14 - pOH_{final} = 8.778$$
Step 3: Calculate the change in pH.
$$\Delta pH = pH_{final} - pH_{initial} = 8.778 - 9.255 = -0.477$$
The magnitude of the change is \( |\Delta pH| = 0.477 \).
Expressing this in the required format: \( 0.477 = 47.7 \times 10^{-2} \).
Rounding to the nearest integer gives 48.
Initial moles: NH3 = 0.10, NH4+ (from NH4Cl) = 0.10. Volume ≈ constant, so Henderson–Hasselbalch (base buffer) applies.
pOHinitial = pKb + log([salt]/[base]) = 4.745 + log(0.10/0.10) = 4.745
pHinitial = 14 − 4.745 = 9.255
Add 0.05 mol HCl: NH3 + HCl → NH4+
New moles: NH3 = 0.10 − 0.05 = 0.05; NH4+ = 0.10 + 0.05 = 0.15
pOHfinal = pKb + log(0.15/0.05) = 4.745 + log 3 = 4.745 + 0.477 = 5.222
pHfinal = 14 − 5.222 = 8.778
ΔpH = pHinitial − pHfinal = 9.255 − 8.778 = 0.477 = 47.7 × 10−2 ≈ 48 × 10−2
Answer: 48
For \( \alpha, \beta, \gamma \in \mathbb{R} \), if \[ \lim_{x \to 0} \frac{x^2 \sin(\alpha x) + (\gamma - 1)e^{x^2}}{\sin(2x - \beta x)} = 3, \] then \( \beta + \gamma - \alpha \) is equal to:

In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by: