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