We present OH observations from NACHTT-11 held at the Boulder Atmospheric Observatory in Weld County, Colorado. Average OH levels at noon were ~ 2.7 × 106 molecules cm−3 at 2 m above ground level (AGL). Nitrous acid (HONO) photolysis was the dominant OH source (80.4%) during this campaign, while alkene ozonolysis (4.9 %) and ozone photolysis (14.7 %) were smaller contributions to OH production. To evaluate recycling sources of OH from HO2 and RO2, an observationally constrained University of Washington Chemical Mechanism (UWCM) box model (version 2.1) was employed to simulate ambient OH levels over several scenarios. For the base run, not constrained by observed HONO, the model significantly underestimated OH by a factor of 5.3 in the morning (9:00 – 11:00) and by a factor of 3.2 in the afternoon (13:00 – 15:00). The results suggest that known chemistry cannot constrain HONO and, subsequently, OH during the observational period. When HONO is constrained in the model by observations (< 50 m), the discrepancy between observation and model simulation improves to a factor of 1.3 in the morning and a factor 1.1 in the afternoon, within the 35 % estimated instrumental uncertainty. However, the model produces both a morning and afternoon maximum in OH, in contrast to the observations, which show strong evidence for morning OH production but no distinct morning maximum. Two additional OH sources were also considered, although they do not improve the differences in modeled and measured temporal OH profiles. First, the impact of daytime HONO gradients near the ground surface (< 20 m) was evaluated. Strong HONO gradients were observed between 06:00 – 09:00 MST (Mountain Standard Time), especially within 20 m of the surface. When constrained to HONO observed below 20 m (rather than 50 m), the model produced an even larger morning OH maximum, in contrast to the observations. Second, Cl atoms from ClNO2 photolysis producing RO2 from reaction with alkanes, while significant, produced steady state Cl atom levels (~ 103 atoms cm−3) that were too low to significantly perturb measured OH through reactions of organic peroxy radicals produced from Cl reactions with VOCs.