Step 1: Understanding the dissociation of \( H_2S \).
\( H_2S \) is a weak diprotic acid that dissociates in two steps:
\[
H_2S \rightleftharpoons H^+ + HS^-
\]
and
\[
HS^- \rightleftharpoons H^+ + S^{2-}
\]
Given \( K_{a1} \) for the first dissociation and \( K_{a2} \) for the second dissociation, we need to calculate the concentration of \( HS^- \) in solution.
Step 2: Consider the first dissociation.
For the first dissociation step, we use the expression for the equilibrium constant \( K_{a1} \):
\[
K_{a1} = \frac{[H^+][HS^-]}{[H_2S]}
\]
Given that the initial concentration of \( H_2S \) is 0.1 M, and the concentration of \( H^+ \) from \( HCl \) is also 0.1 M (strong acid dissociates completely), we can substitute into the equation:
\[
K_{a1} = \frac{(0.1 + x)(x)}{0.1 - x}
\]
Since \( K_{a1} \) is small (\( 8.3 \times 10^{-8} \)), we can assume that \( x \) is very small compared to 0.1, so the equation simplifies to:
\[
K_{a1} = \frac{(0.1)(x)}{0.1}
\]
Thus, solving for \( x \) (which is the concentration of \( HS^- \)):
\[
x = K_{a1} = 8.3 \times 10^{-8} \, \text{M}
\]
Step 3: Consider the second dissociation.
The second dissociation of \( HS^- \) is very weak, with \( K_{a2} = 10^{-13} \), so the concentration of \( S^{2-} \) formed will be negligible. Therefore, the concentration of \( HS^- \) will primarily be determined by the first dissociation.
Final Answer: \( 8.3 \times 10^{-8} \, \text{M} \)