Single-walled carbon nanotubes (SWCNTs) have unique photophysical properties that render them an important class of materials for future nanoelectronics and bio-nano sensor applications. A method was recently discovered for making spatially patterned modifications to SWCNT band gaps and thereby modulating their electronic and optical properties in a controlled manner. The reaction used for this is called guanine functionalization.1 It is achieved by generating singlet oxygen in a dispersion of SWCNTs coated with single-stranded DNA, resulting in covalent bond formation between the guanine nucleobases in the DNA coatings and the nanotube sidewalls. Each of the many covalently bonded guanine sites acts as a weak exciton trap, causing red-shifted SWCNT emission and absorption spectra. Fluorescence spectroscopy shows that the extent of guanine functionalization can depend strongly on SWCNT structure, but spectral broadening can hamper the precise deconvolution of emission features of different (n,m) species. To track such covalent functionalization through Raman scattering, the D to G band ratios are commonly used as a measure of sp3 defect density and therefore of the functionalization extent. However, this conventional Raman method cannot show which (n,m) species in unsorted samples have been functionalized, because they all contribute to the D and G band signals. We will describe a novel Raman analysis based on the relative intensities of bands that have shifts located between the RBM and D regions. These Raman features are found to be diameter-specific, allowing estimation of (n,m)-resolved functionalization extents in unsorted SWCNT samples. In addition, we will present an assignment and interpretation of the relevant Raman features. Zheng, Y.; Bachilo, S. M.; Weisman, R. B., Controlled patterning of carbon nanotube energy levels by covalent DNA functionalization. ACS Nano 2019, 13, 8222-8228.