Ozone reacts with alkenes and other organic compounds that contain carboncarbon double bonds to form oxidation byproducts such as aldehydes, ketones, carboxylic acids, radicals, and secondary organic aerosol. Ozone-reactive species such as terpenes and unsaturated fatty acids are ubiquitous in the air and on surfaces in indoor environments. The most prevalent source of ozone indoors is ventilation of the space with ozone-containing ambient air, although some appliances that are used indoors also produce ozone. Reactions with surfaces are the ever-present and dominant sink of ozone and source of oxidation byproducts. Gas-phase ozone reactions must compete with the ventilation rate; they can be intermittently important ozone consumers and byproduct generators. Ozone-alkene reactions are chain-initiating because radicals are formed that 2 continue to react. The hydroxyl radical (OH) is a major secondary byproduct of ozonealkene chemistry, and it is a less-selective, faster reacting oxidizer than ozone. Thus, species that do not readily react with ozone, i.e. compounds that do not contain a carboncarbon double bond, may also be oxidized by the OH radical in ozone-initiated chemistry.In this dissertation, the chemical and physical factors that affect transformation of ozone into other airborne pollutants in occupied indoor environments are explored.Ozone-initiated reaction with, and byproduct formation from, reactive gas-phase and surface-phase species common to indoor settings were investigated in four studies.Byproduct types and formation rates were characterized in laboratory experiments.Byproduct concentrations and exposures were predicted in various indoor environments using experimental data and a model that predicts ozone transport and uptake and byproduct formation and fate.When both ozone and terpenes are present in indoor settings, terpenes can be a strong sink of ozone and source of gas-and particle-phase byproducts. I investigated secondary organic aerosol formation from the reaction of ozone with terpene-containing consumer products under conditions relevant for residential and commercial buildings.Gas-phase consumer product emissions and then ozone were introduced into a continuously ventilated 198-L chamber. At the onset of ozone addition, a nucleation event occurred, and nucleation and growth continued to occur as long as the reagents were introduced into the chamber. The particle formation and growth behavior in these experiments mimicked SOA dynamics from ozone-terpene reactions measured in actual buildings. The full particle size distribution was continuously monitored using an optical 3 particle counter and scanning mobility particle sizer. The resulting ultrafine and fine particle concentrations were in the range of 10 to >300 µg m -3 . Particle nucleation and growth dynamics under indoor conditions were characterized using the methods commonly applied to atmospheric nucleation events.Commercial passenger aircraft can encounter elevated stratospheric ozone levels at cruising altitude, and because...