Step 1: Understanding the Concept
Aldehydes without alpha hydrogen undergo the Cannizzaro reaction with concentrated alkali. One molecule is oxidised and another is reduced.
Step 2: Reaction
\(2\text{C}_{6}\text{H}_{5}\text{CHO}+\text{NaOH}\rightarrow\text{C}_{6}\text{H}_{5}\text{CH}_{2}\text{OH}+\text{C}_{6}\text{H}_{5}\text{COONa}\). Benzyl alcohol is the reduced product.
Step 3: Why the other options fail
Wurtz, Fittig and Wurtz-Fittig reactions couple alkyl or aryl halides with sodium and do not involve aldehydes.
Final Answer:
Benzaldehyde gives benzyl alcohol by Cannizzaro's reaction.
\[ \boxed{\text{(D) }\text{Cannizzaro's reaction}} \]