To get you started I'll suggest finding elements of unsaturation. This tells you how many pi bonds and/or rings will be present in any isomer with a given molecular formula. Each pi bond and ring connection removes 2 hydrogens from your molecular formula.
For saturated compounds containing only carbon, hydrogen and oxygen we expect 2N+2 hydrogens, where N equals the number of carbons. Try drawing any compound with just those elements and you'll see this is true.
Now for calculating the # of elements of unsaturation there is a handy formula you can use: ((2N+2)-(# of hydrogens in actual compound))/2
I like to think of it as (expected number of hydrogens minus actual number of hydrogens)/2