This is a two-step reaction:
1. Friedel-Crafts acylation:
\[
\text{C}_6\text{H}_6 + \text{CH}_3\text{CH}_2\text{COCl} \xrightarrow{\text{AlCl}_3} \text{C}_6\text{H}_5\text{COCH}_2\text{CH}_3
\]
Phenylpropanone (aromatic ketone) is formed.
2. Clemmensen reduction:
\[
\text{C}_6\text{H}_5\text{COCH}_2\text{CH}_3 \xrightarrow{\text{Zn-Hg/HCl}} \text{C}_6\text{H}_5\text{CH}_2\text{CH}_2\text{CH}_3
\]
The carbonyl group is reduced to -CH\(_2\)-, giving n-propylbenzene.
Hence, the final product is:
\[
\boxed{\text{C}_6\text{H}_5\text{CH}_2\text{CH}_2\text{CH}_3}
\]