SAFETY: Carvone is an irritant.
Carvone gives spearmint gum its flavor!
1. Make a list of each functional group in carvone
For every double bond, indicate whether it's conjugated or saturated
2. Go to the IR Table of Values (keep this open in a separate tab)
Find each functional group, corresponding bonds, and expected wavenumber ranges.
Include notes about peak shape: broad, strong, medium, weak
There are two different types of alkenes in carvone. List these as separate functional groups.
Notice the C-H bend region is large, go to Table 2 of the reference table to get a closer approximation of bending frequency based on substitution pattern of the alkene
Enter this information into a table, format below.
Follow the "expected wavenumber range" in your table, look for a signal that corresponds to each.
Enter the corresponding wavenumber from the spectrum below in the literature column of the carvone table
Some signals may not be labeled and some signals may overlap with others
It is not necessary to assign every signal indicated in the spectrum to a bond
Follow the "expected wavenumber range" in your table, look for a signal that corresponds to each
Enter the corresponding wavenumber from the spectrum below in the observed column of the carvone table
Some signals may not be labeled and some signals may overlap with others
It is not necessary to assign every signal indicated in the spectrum to a bond
What differences and similarities are there in the literature vs. observed spectra?
How does this spectrum exemplify the relationship between bond length and wavenumber (vibrational frequency)?
Common mistakes: not adding enough sample to the NaCl plates.
Click the button on the right to see what not to do before analyzing methyl salicylate and aspirin.