Step 1: Understanding the Concept:
Cannizzaro reaction is the disproportionation of aldehydes that have no alpha hydrogen, when treated with concentrated alkali.
Step 2: What happens:
One molecule of the aldehyde is oxidised to a carboxylate salt, and another is reduced to an alcohol. For example
\[ 2HCHO + NaOH \rightarrow CH_3OH + HCOONa \]
Step 3: Check the options:
(A) says some aldehydes give the alcohol and the salt of the acid, which is exactly this. (B) Alcohol to aldehyde is an oxidation, not Cannizzaro. (C) Amine to isocyanide is the carbylamine reaction. (D) Acid to amine is a Hofmann or Schmidt type change. So (A) is true.
Final Answer:
Cannizzaro gives an alcohol and a carboxylate salt.
\[ \boxed{A} \]