Using the following spectra and other information provided, identify the compounds, and all pertinent peaks are assigned in the spectra (correct compound, labeling proton spectrum, labeling carbon spectrum) Label the peaks on the spectrum and place the structure of the compound in the box on the right side of the spectrum.
Using the following spectra and other information provided, identify the compounds, and all pertinent peaks are assigned in the spectra (correct compound, labeling proton spectrum, labeling carbon spectrum)
Label the peaks on the spectrum and place the structure of the compound in the box on the right side of the spectrum.
In 1H nmr we get signal due to proton which are magnetically and chemically non equivalent
In nmr the splitting pattern is determined by the formula 2nI +1
Where I is nuclear spin and for hydrogen it is 1/2
n is number of equivalent hydrogen
Similarly in 13 C mmr we get signal due to carbon which are magnetically and chemically non equivalent
If there is any symmetry element present present in the compound then number of signal will be lesser than actual number of carbon
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