The catalytic cracking behavior of compound types in the >650°F resid from a Wilmington, CA, 14.2°API crude was investigated. Liquid Chromatography (LC) was used to sepm'ate the resid into eight fractions. These fractions were used as feedstocks for a bench scale fluidized catalytic cracking (FCC) unit. Gasoline was produced almost exclusively from neutral (65 % of whole resid) components. Acidic and basic types were partially converted to coke plus small amounts of C! and C2 gases, with the balance primarily carrying over as heavy liquid products. Gasoline composition depended on the type and quantity of polar compounds present in the feed because both acidic and basic compounds inhibited cracking reactions (13-scission, hydrogen transfer, etc.) to varying degrees. In accordance with prior work, basic nitrogen compounds exhibited the largest inhibitory effect on cracking. Their effect is dependent on concentrations up to a limiting value which may correspond to saturation of susceptible catalyst sites. On an equal weight basis, the effect of high boiling (high molecular weight) bases was less than those occurring in the 650-1000°F distillate range. Pm'titioning of nitrogen present in acidic (e.g. carbazole) forms in the feed into liquid products was greater than for basic nitrogen. Thiophenic forms of sulfur partitioned more into liquid and less into gaseous (H2S) products than sulfide-type sulfur. Coke yield was approximately proportional to microcarbon residue test results for all feeds. Ongoing work with additional feedstocks has indicated behavior similar to that of Wilmington. Selected Wilmington liquid products are undergoing detailed analysis in order to determine relationships between feed versus product composition, particularly with respect to acidic and basic types.