Step 1: Rule out the other named reactions first.
Benzene with CO/HCl over anhydrous $\text{AlCl}_3$ is Gattermann-Koch formylation, and acid chloride with $\text{H}_2$ over Pd-BaSO4 is Rosenmund reduction, both genuine routes to benzaldehyde but neither is Etard's reagent.
Step 2: Pin down what actually defines the Etard reaction.
It's specifically chromyl chloride ($\text{CrO}_2\text{Cl}_2$) oxidising a toluene-type methyl group, forming a brown chromium complex in $\text{CS}_2$ solvent.
Step 3: Complete the sequence.
That complex is then hydrolysed with dilute acid to release the aldehyde product.
Step 4: Match this to the options.
Toluene with $\text{CrO}_2\text{Cl}_2$ in $\text{CS}_2$ followed by aqueous workup is exactly the first option.
Final answer: Option 1.