(Solved): 1H NMR Workshop This packet contains 15 1H NMR spectra that correspond to the 15 IR spectra yo ...
1H NMR Workshop
This packet contains 15 1H NMR spectra that correspond to the 15 IR spectra you interpreted earlier this semester. For example, the IR and NMR spectra labeled “A” are from the same compound “A”. The IR spectra for many of these compounds resulted in several possible isomers. Now you can combine the information from the 1H NMR spectra to narrow down the list of possible structures. For those compounds where the IR data resulted in a single isomer, demonstrate why the NMR data confirm this structure.
Draw the structure of each compound on its NMR spectrum and CLEARLY indicate which protons create their respective signal – for example, the protons labeled ‘a’ create signal ‘a’. You will be scored on the thoroughness and accuracy of your NMR interpretation and the correct prediction of the molecular structure for each compound. As always, you may work in groups and are encouraged to take a moment to evaluate the correctness of your own final answers.
Note: The spectra in this workshop also include 13C NMR, for now, you are going to ignore the carbon NMR spectra information. We will come back to C NMR at the end of the semester.
Please answer this question correctly and follow the guidelines (do not give me an incorrect answer). I need it soon. Thank you in advance.
