Step 1: Identify the starting compound.
The given alcohol is propan-1-ol:
\[
\mathrm{CH_3CH_2CH_2OH}
\]
Step 2: Reaction with HCl/ZnCl\(_2\).
HCl in the presence of ZnCl\(_2\) (Lucas reagent) converts alcohol into alkyl chloride.
Thus, propan-1-ol forms 1-chloropropane:
\[
\mathrm{CH_3CH_2CH_2OH \rightarrow CH_3CH_2CH_2Cl}
\]
Step 3: Reaction with NaI in dry acetone.
This is the Finkelstein reaction.
Alkyl chloride is converted into alkyl iodide:
\[
\mathrm{CH_3CH_2CH_2Cl \rightarrow CH_3CH_2CH_2I}
\]
Thus, 1-iodopropane is formed.
Step 4: Reaction with Na in dry ether.
Alkyl iodide reacts with sodium metal in dry ether through the Wurtz reaction.
Two propyl groups combine together:
\[
2\mathrm{CH_3CH_2CH_2I}+2\mathrm{Na}
\rightarrow
\mathrm{CH_3CH_2CH_2CH_2CH_2CH_3}+2\mathrm{NaI}
\]
Step 5: Identify the final product.
The product formed contains six carbon atoms in a straight chain.
Hence, the final product is hexane.
Step 6: Final conclusion.
Therefore, the major product formed is
\[
\boxed{\text{Hexane}}
\]