The question asks for the multiplicity of the $^{13}C$ NMR signal for DMSO-$d_6$ at $\delta$ 39.7 ppm. This signal corresponds to the methyl carbons.
DMSO-$d_6$, or deuterated dimethyl sulfoxide, has the structure $(CD_3)_2S=O$. The key feature affecting the splitting of the $^{13}C$ signal is the presence of deuterium ($D$) atoms attached to the methyl carbons.
In NMR spectroscopy, the splitting of a signal depends on the coupling between the observed nucleus ($^{13}C$) and nearby nuclei with non-zero spin. Deuterium ($D$) has a nuclear spin quantum number $I = 1$.
The multiplicity of the $^{13}C$ signal is determined by the number of equivalent deuterium atoms coupled to it, using the formula for signal splitting:
$ \text{Number of lines} = 2nI + 1 $Where:
In DMSO-$d_6$, each methyl carbon is bonded to three deuterium atoms ($n=3$). The spin of deuterium is $I=1$.
Plugging these values into the formula:
$ \text{Number of lines} = (2 \times 3 \times 1) + 1 = 6 + 1 = 7 $A signal split into 7 lines is known as a septet.
Therefore, the $^{13}C$ NMR signal of DMSO-$d_6$ at $\delta$ 39.7 ppm appears as a septet due to coupling with the three deuterium atoms.
In $^1H$ NMR, the multiplicity pattern expected for the highlighted protons in the following compounds is

The number of signals observed in the proton decoupled $^{13}\text{C}$ NMR spectrum of the following compound is