To find the molar solubility of \( AX \) in a 0.1 M \( HX \) solution, we begin with the dissolution equilibrium of \( AX \):
\[ AX(s) \rightleftharpoons A^+(aq) + X^-(aq) \]
The solubility product (\( K_{sp} \)) is given by:
\[ K_{sp} = [A^+][X^-] = 10^{-10} \]
However, since the solution contains 0.1 M \( HX \), which is a strong acid, it dissociates completely:
\[ HX \rightleftharpoons H^+ + X^- \]
This means that the concentration of \( X^- \) ions from \( HX \) in the solution is initially 0.1 M. Let the solubility of \( AX \) in this solution be \( s \). Then at equilibrium:
\[ [A^+] = s \]
\[ [X^-] = s + 0.1 \approx 0.1 \] (since \( s \) is small compared to 0.1)
Substituting these into the \( K_{sp} \) expression, we get:
\[ 10^{-10} = s \times 0.1 \]
Solve for \( s \):
\[ s = \frac{10^{-10}}{0.1} = 10^{-9} \]
Thus, the molar solubility of \( AX \) in 0.1 M \( HX \) solution is \( 10^{-9} \) M.