Question

I'm trying to figure out some incorrect answers on my last test. I'll try to explain what the original structure looks like and hope you can decipher it.

It is a cyclohexane with two double bonds. Carbon # 1 has a double bond to its left and none to its right. It has one substituent which is OCH3. Carbon 2 has no double bonds to right or left and has two H substituents. Carbon 3 has no double bonds and has a +. What are the resonance structure(s)?

Thanks from Sheryl