The last part, where you put oxygen and the organic compound in a container is actually very important. If you were to put CH
3* and oxygen in a container, the first thing you have on your hand is a load of shrapnel, as CH
3* is a radical and a pretty nasty one at that. You actually can't have isolated CH
3* at moderate temperatures, you have to heat ethane (c
2H
6) up to fairly high temperatures to even get a bit of it to fracture into radicals (and you're going to get it mixed with other fun stuff such as H* and C
2H
5*, not to mention rubbish such as atomic carbon)
Now what you've actually got on your hands is an organic compound with the empirical formula C
nH
3n. Now, you can use the density you get when mixed with oxygen to obtain the molar weight and from that you can find the right compound.
Problem is the third question. Assuming we're really dealing with C
nH
3n, a reaction with Br
2 should either result in the breaking of a carbon-carbon bond, yielding two moles of an organic bromide, or you get Br
2 -> 2 Br*, Br*+ C
nH
3n -> C
nH
3n-1Br + H*, meaning you're going to get H
2 and HBr as side products. From that I presume that you've made an error in calculating the molar ratios in your compound and you're actually dealing with an alkene, in which case you're getting addition of bromide across a double bond (which is actually a pretty awesome process if you look closer at it, see
this), which would result in a single molecule.
Edit: wat? Huh? I can't find any errors in your calculation? That's odd. You may want to double check the figures with your teacher because you can't get ethane (the only compound with the formula C
nH
3n that isn't something nasty) to react with bromine and yield only 1 compound, you'd get pentavalent carbon atoms and stuff like that...