Ah, you are right, you do need to move it to C3. Why would it be favorable to move there? Just as a hint, such a move would be called a hydride shift if you arent familiar with it. Typically we do not draw this shift as an arrow push, its just shown that the + moves spontaneously to give a more stable carbocation (though I guess you could draw the arrow).
Once you move it then and attack with the double bond how might we reform aromaticity? Remember some kinda difficult reactions can happen because aromaticity is so heavily favored (24 kcal/mol!)