We describe a nearly explicit chemical mechanism for isoprene photooxidation guided by chamber studies that include time-resolved observation of an extensive suite of volatile compounds. We provide new constraints on the chemistry of the poorly-understood isoprene ÎÂ´-hydroxy channels, which account for more than one third of the total isoprene carbon flux and a larger fraction of the nitrate yields. We show that the cis branch dominates the chemistry of the ÎÂ´-hydroxy channel with less than 5% of the carbon following the trans branch. The modelled yield of isoprene nitrates is 12$\pm$3% with a large difference between the ÎÂ´ and ÎÂ² branches. The oxidation of these nitrates releases about 50% of the NOx. Methacrolein nitrates (modelled yield 15$\pm$3% from methacrolein) and methylvinylketone nitrates (modelled yield 11$\pm$3% yield from methylvinylketone) are also observed. Propanone nitrate, produced with a yield of 1% from isoprene, appears to be the longest-lived nitrate formed in the total oxidation of isoprene. We find a large molar yield of formic acid and suggest a novel mechanism leading to its formation from the organic nitrates. Finally, the most important features of this mechanism are summarized in a condensed scheme appropriate for use in global chemical transport models.