The reaction described is an example of the Cannizzaro reaction, which occurs when an aldehyde (lacking an α-hydrogen) is treated with a strong base (like concentrated sodium hydroxide). The reaction leads to disproportionation, where one molecule is reduced to an alcohol, and the other is oxidized to a carboxylate anion.
In this case:
- p-Methoxy benzaldehyde undergoes the Cannizzaro reaction.
- Methanal (formaldehyde) also undergoes the same process.
The main products:
- The reduction of one aldehyde molecule (in this case, p-Methoxy benzaldehyde) leads to the formation of p-Methoxy benzyl alcohol.
- The other aldehyde (formaldehyde) is oxidized to form sodium formate.
Therefore, the correct products are p-Methoxy benzyl alcohol and sodium formate.