Optical isomers are compounds which are mirror images of each other, so are non-superimposable. Like, no matter how you rotate the compound, they would never be exactly the same as the other.
This feature does come from having a chiral carbon. A chiral carbon is bonded to four different groups.
So, if a carbon atom is bonded to a hydrogen, a hydroxy, a methyl and an ethyl group, it would be chiral for example.
Oh, and double bonds would make that carbon not chiral.
I don't really get the question in the past paper that you have, so leaving that for someone else to answer, but I hope this clarifies chirality and optical isomers for you.