Electrophilic substitution reaction

Hi, I need to do this exercise. I understand that the most reactive ring is the one on the right because its substituent is more activating than the substituent attached to the left ring. Furthermore, it's an ortho/para-directing substituent. There's no problem with the ortho product, but with the para product, I see that it's not possible to restore the ring's aromaticity. Will this para product still form?