Step 1: Understanding the reaction.
Anisole (methoxybenzene) reacts with concentrated H\(_2\)SO\(_4\) and HNO\(_3\) to undergo nitration, which substitutes a nitro group (-NO\(_2\)) on the aromatic ring. The reaction typically gives a mixture of ortho and para products due to the electron-donating effect of the methoxy group.
Step 2: Conclusion.
The reaction yields a mixture of ortho and para products.
