Although I agree that these spectra could have been better, I think they are sufficiently acceptable to determine a structure. I suggest you determine a hydrogen ratio from the NMR. Hydrogens come in 1s, 2s, and 3s. It has already been suggested that you have an ethyl group. Therefore you know that there is XH, 2H, YH, 3H. What are or could be X and Y? The big peak at 7.24 is not chloroform, it is your compound. Determining X and Y from the integral should give a big clue. You virtually have only two or three atoms to move around. Draw out some possibilities with those atoms.
If you can re-run your IR, do so. It is much too strong to make a comparison with authentic samples. You will find authentic samples do not max out the absorbance at every peak as the posted spectrum has. If you cannot re-run it, it is still good enough, but you need to mentally reduce the absorbances. What are big peaks in your spectrum are actually small peaks in an authentic spectrum.
Look at the "Tinker Toy" method I was suggesting in this
problem. Look at your spectrum. Write down on paper what each piece could be. If you have a CH3 group, what must it be attached to? What other groups can you discern? Can you tell what atoms they may be attached to? If you have more than one possibility, write them down in a group.
Hint, there isn't any absorption at <3050 cm
-1 and your compound only contains C, H, and O. When I put the pieces together, I could only come up with one possibility. I don't know how many anyone else may come up with, but I cannot emphasize enough to write on paper the pieces you are trying to place and some possible structures. You can test possible structures against your spectral data and decide if a piece is right, nearly right, could be right with some adjustment, or can be excluded. Your NMR has four signals and two you know something about. There are two additional signals you should be able to figure out from the integral. There are some additional atoms that do not give signals in the NMR, but the chemical shifts and IR certainly strongly suggest what they are. Given that information, it shouldn't be that hard (provided you write something on paper).