Step 1: Understanding the dissociation of \( H_2S \).
Hydrogen sulfide (\( H_2S \)) is a weak diprotic acid that ionizes in two successive steps:
\[
H_2S \rightleftharpoons H^+ + HS^-
\]
\[
HS^- \rightleftharpoons H^+ + S^{2-}
\]
We are required to determine the concentration of \( HS^- \) in the presence of a strong acid.
Step 2: Analyze the first dissociation equilibrium.
For the first dissociation, the equilibrium constant expression is:
\[
K_{a1} = \frac{[H^+][HS^-]}{[H_2S]}
\]
The initial concentration of \( H_2S \) is \( 0.1 \, \text{M} \), and the concentration of \( H^+ \) supplied by the strong acid (HCl) is also \( 0.1 \, \text{M} \). Let the concentration of \( HS^- \) formed be \( x \).
Substituting into the equilibrium expression:
\[
K_{a1} = \frac{(0.1)(x)}{0.1 - x}
\]
Since \( K_{a1} = 8.3 \times 10^{-8} \) is very small, the value of \( x \) will be negligible compared to \( 0.1 \). Therefore, we approximate:
\[
0.1 - x \approx 0.1
\]
Thus, the expression simplifies to:
\[
K_{a1} = \frac{(0.1)(x)}{0.1}
\]
\[
x = K_{a1}
\]
\[
x = 8.3 \times 10^{-8} \, \text{M}
\]
Step 3: Consider the second dissociation.
The second dissociation constant \( K_{a2} = 10^{-13} \) is extremely small, indicating that the further ionization of \( HS^- \) to form \( S^{2-} \) is negligible. Hence, the concentration of \( HS^- \) is mainly governed by the first dissociation step.
Final Answer: \( [HS^-] = 8.3 \times 10^{-8} \, \text{M} \).