Only in relatively rare cases can UV/VIS be used to determine a structure.
Having said that, lets go a little further. Typically, when you are analyzing a solution by UV/VIS, you have a general idea of the ingredients. You have a solution that may contain phenols. Phenols typically absorb at 280 nm. You run the uv vis and find there is no peak in the 280 nm range. It's a good bet that no phenols are present.
Another example. I have an unknown, and it shows a peak in the UV/VIS at 280 nm. The first ingredients I'll investigate are phenols. It's not proof a phenol is present, but it gives a good hint.