We are given the solubility product of \( AX \) as \( K_{sp} = 10^{-10} \) at \( T(K) \).
Let the molar solubility of \( AX \) be \( s \) in pure water. So, the dissociation of \( AX \) is represented as:
\[
AX (s) \rightleftharpoons A^+ (aq) + X^- (aq),
\]
where the concentration of \( A^+ \) and \( X^- \) will both be \( s \) in pure water. Therefore, the solubility product is:
\[
K_{sp} = [A^+][X^-] = s^2.
\]
Thus, the solubility \( s \) in pure water is:
\[
s = \sqrt{K_{sp}} = \sqrt{10^{-10}} = 10^{-5} \, {mol/L}.
\]
Now, in the presence of \( 0.1 \, {M} \) HX, the concentration of \( X^- \) ions is increased by the dissociation of HX. Since HX dissociates fully:
\[
{[X}^-] = 0.1 \, {M} + s.
\]
Now, the solubility product equation becomes:
\[
K_{sp} = [A^+][X^-] = s(0.1 + s).
\]
Since \( s \) is much smaller than 0.1, we can approximate \( 0.1 + s \approx 0.1 \). Therefore, the equation simplifies to:
\[
K_{sp} = s \cdot 0.1.
\]
Substituting the value of \( K_{sp} = 10^{-10} \):
\[
10^{-10} = s \cdot 0.1,
\]
\[
s = \frac{10^{-10}}{0.1} = 10^{-9} \, {mol/L}.
\]
Thus, the molar solubility of \( AX \) in 0.1 M HX solution is \( 10^{-9} \, {mol/L} \).