Predict the NMR spectra by listing in the NMR table the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest.

How many 13C NMR signals does attached compound exhibit ?

Assign each peak with the number in the molecular formula.  Explanations will very much be appreciated.

Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest.

14. How many distinct signals are in the ¹³C NMR of the following compound?

How many 13C NMR signals does attached compound exhibit ?

How many unique 1°C NMR signals exist in the spectrum for the compound? HO HO, The number of signals is:

A.) How many signals are seen for the CNMR spectrum of the unknowns C6H14O? B.) Explain the chemical shifts of the signals seen based upon the location of the carbons that are relative to deshielding group if any are seen in the compound (unknown is C6H14O)?  For question A. I believe it is 4 signals. For question B. I know that none of the signals are in the deshielding are of the chart but are all located in the shielded region but i am unsure of how to determine the chemical shifts of the given signal. If possible an in-depth explanation would be greatly appreciated in order to understand this better.

3. For the structure shown, assign the signals to the respective hydrogen and carbon on the HNMR and CNMR spectra given below. O n R

Arrange the following compounds in their correct order of chemical shift (). 1=Highest and 4=lowest. (All show just one signal in their 1HMR spectrum).