Describe how this "dried product" is often different from a crystallized product. (Describe the two different products on a molecular level.)

CH, AIC13

Provided are spectra for a compound with molecular formula CgH100 Part A) Give the degrees of unsaturation Part B) Identify the peaks that are associated with specific bonds of the structure and list the corresponding functional groups that the specific bonds belong to. Re- create the example table below that organizes this information. Use the wavenumbers that are already labeled on the spectra. Example table: wavenumber (cm-1) Corresponding Bond Type Corresponding Functional Group C(sp3)-H N-H 2978 3300 Part C) Draw the structure and clearly indicate which hydrogens correspond to which signals in the HNMR spectrum ONLY. The signals are already labeled A-D on the HNMR spectrum. Match the hydrogen labeling (HA, HB, etc.) on your drawn structure to the signal labeling provided. 4300 3320-2872 2951 3006 3003 2001 alkyl amine 1613 1510 1000

See Figure 13-10. Which structure best matches the NMR and IR shown? O A B