This is a combined structure problem; using the spectral data provided we are to identify the compound. I've attached the image of the spectra here.
Uploaded with
ImageShack.usMy thinking is:
The IR suggests an aromatic alcohol: the stretch at 1600cm-1 is too low to be attributed to a carbonyl. The sp2 and sp3 C-H stretches and the stretches in the 1450-1600cm-1 range suggest an aromatic ring.
From the mass spec and thep revous IR data, I think the formula is C12H14O.
From the proton NMR I get: the upfield triplet is from a CH3, the multiplet at 1.9ppm is from the CH2 in a Ar-CH2-CH3 substituent.
The 3.4ppm quartet is from a Ar-CH(OH)-CH3.
The signals in the aromatic region are from the four aromatic hydrogens in an ortho-disubstituted arrangement (two doublets, two triplets).
The singlet at 5.9 ppm or so is from the O-H.
I believe the molecule to be:
Uploaded with
ImageShack.ushttp://imageshack.us/photo/my-images/845/aromaticalcohol.jpg/I'm not sure what it's called.
Would this be correct:? Have I missed anything?
Thanks alot