Functionalization of carbon nanotubes (CNTs) with heteroatoms enables covalent attachment, opening up a world of potential material structures. However, common functionalization techniques are hazardous and lack precision. Here, we evaluate an in situ functionalization technique using oxygen-containing alkyne precursors. CNTs were successfully derived from propargyl alcohol and propiolic acid, at 67±7 and 19±3 µm min -1 , respectively. While there was no substantial increase in the oxygen content of resultant CNT structures (all less than 1% O), Fourier transform infrared spectroscopy revealed subtle incorporations of carboxyl and hydroxyl functionality. An analysis of reactor effluent showed that both oxygen-containing species shed oxygen groups, where propargyl alcohol yielded a reactive atmosphere high in methylacetylene, and propiolic acid thermally degraded to acetylene and CO2, potentially explaining the enhanced catalyst lifetimes (approximately 75 min). These results support the universality of alkynepromoting chemistries and delineate the limits of stable, oxygen-bearing alkynes to support point-directed functionalization schemes.