Step 1: Identify the directing group
The methoxy group donates electrons by resonance, so it activates the ring and directs to ortho and para.
Step 2: Nitration
With HNO\(_3\)/H\(_2\)SO\(_4\) the electrophile is NO\(_2^+\). It attacks the ortho and para positions.
Step 3: Major product
The para product is major because the ortho positions are hindered by the OCH\(_3\) group. So the major product is 4-nitroanisole.
Nitrophenols are wrong because the ether group is not cleaved under these conditions.
Final Answer:
The major product is 4-nitroanisole, option (B).
\[ \boxed{\text{(B)}} \]