Which 2 resonance forms destablize the carbocation intermediate if bezonitrile undergoes chlronation at the ortho or para positions

The question is incomplete, the complete question is shown in the image attached

A and B

Explanation:

The electrophilic substitution of arenes yields a cation intermediate. The positive charge of the cation is delocalized over the entire ring.

The -CN group directs incoming electrophiles to the ortho/para position. The resonance structures for the chlorination of benzonitrile are shown in the question.

Recall that -CN is an electron withdrawing group. The resonance forms that destablize the carbocation intermediate are those in which the -CN group is directly attached to the carbon atom bearing the positive charge as in structures A and B.

is there multiple choice answers?