As Klaus and I mentioned, the first reactions seem very strange from a chemical perspective, even if they are correctly balanced. This is where a chemist needs to exercise their intuition and experience.
Balancing reactions is nothing but solving a linear system of equations, so it is entirely possible to propose reactions which balance perfectly, but which are based on questionable chemistry. For example, in all but the last reaction, the sulphur atoms in $\ce{SO_4^2-}$ anions are being reduced to lower oxidation states. While this is possible in some conditions, it takes quite strong reducing agents, and none of the reagents shown are known to possess significant reducing character. Reactions which release gaseous oxygen are also not particularly common. Furthermore, two reactions propose the formation of sulphur chlorides, which would actually hydrolyse in contact with water.
Disregarding intuition, it should be possible to pick out which reaction is the most favourable by simply comparing the Gibbs free energy of reaction in each case; the most exergonic reaction, with the most negative value of $\boldsymbol{\Delta_\mathbf{r}G}$, should dominate (assuming no kinetic factors bar it from happening, which is unlikely in this situation). I did a very quick and dirty calculation, out of curiosity, by taking the standard Gibbs free energy of formation $\Delta_\mathrm{f}G^\circ$ for each compound and summing them together to obtain the standard Gibbs free energy of reaction:
$$\Delta_\mathrm{r}G^\circ = \sum\limits_\text{products}\Delta_\mathrm{f}G^\circ - \sum\limits_\text{reagents}\Delta_\text{f}G^\circ$$
This is only meant as a qualitative way to compare the reactions, as I am assuming standard state conditions for the reactions, which are not necessarily true. Furthermore, for a few species, I didn’t find the correct values in these two sources [1] [2]. $\ce{SCl2}$ and $\ce{S2Cl2}$ probably can’t be found tabulated for the aqueous phase because of their propensity to hydrolysis, so I used the free energies of formation for the gas and solid phases, respectively. I also didn’t find a source for aqueous $\ce{Na2SO4}$, so instead I used the data for the solid decahydrate $\ce{Na2SO4 . 10 H2O (s)}$. The results I got were:
$$ \small
\begin{array}{lcc}
\hline
\text{Reaction} & \Delta_\mathrm{r}G^\circ / \mathrm{kJ\ mol^{-1}}\\
\hline
\text{A} & +440 \\
\text{B} & +1940 \\
\text{C} & +590 \\
\text{D} & \mathbf{-2610} \\
\hline
\end{array}
$$
As you can see, even though the calculation was very rough, the huge disparity in free energy values suggests that the first three reactions are completely overwhelmed by the last one, so that of the four possibilities listed, only the last has any chance of occurring. Strictly speaking this doesn’t mean the last reaction happens, only that it’s much more favourable than the others presented; there could be an unlisted reaction which is even more favourable than all four mentioned in the question. However, empirical data confirms that the last reaction, a simple neutralisation reaction, is the major event when mixing $\ce{HCl}$, $\ce{H2SO4}$ and $\ce{NaOH}$ in practically any conditions.