What is the expected integral ratio?
What would the expected integral ratio calculated from a 1H-NMR spectra for this compound be?
What is the functional group represented by A
Incorrect - Ethers generally have a peak responses between 3.2 and 3.8ppm
Try and match up the functional groups (red, blue and black) with the corresponding group of peaks on the NMR spectra (A, B or C)
If you have 3 out of 3 well done you are CORRECT. If not please read the notes below and try again
The functional group CH2 (black) is surrounded by 4 hydrogens, therefore following the n + 1 rule corresponds to a quintet
The functional group CH2 (blue) has 5 neighbouring hydrogens there it corresponding signal has 6 peaks
There are two terminal CH3 (red) which gives rise to the higher peak heights. They are surrounded by only 2 neighbouring hydrogens therefore there signal is a triplet
Please read the notes below and try again
Match the functional groups (red and blue) with there corresponding clusters of peaks (A or B) on the NMR spectra
If you have 2 out of 2 - Well done you are CORRECT
The CH2 (blue) functional group has a higher chemical shift value than normal because of the deshielding effect of the nitrogen. It has 3 neighbouring hydrogens and is represented by a quadruplet
The CH3 (red) functional group has a lower chemical shift and is represented by a triplet on the spectra which represents the 2 neighbouring hydrogens
You have got one answer wrong - look at the notes below and try again
How many proton types are found in ethane?
Incorrect - Six it the total number of hydrogen molecule present
How many proton groups are there in triethylamine?
What compound is represented by the spectra above
Correct - Well done
Notice the slight dissociation of the peaks associated with the benzene ring due to the deshielding effect of the ketone group. The two hydrogens adjacent to the ketone group have a slightly higher chemical shift value
What compound does the above proton NMR spectra represent