Singlet fission, the creation of two triplet excitons from one singlet exciton, is being explored to increase the efficiency of solar cells and photo detectors based on organic semiconductors, such as pentacene and tetracene. A key question is how to extract multiple electron-hole pairs from multiple excitons. Recent experiments in our laboratory on the pentacene/C-60 system (Chan, W.-L.; et al. Science 2011, 334, 1543-1547) provided preliminary evidence for the extraction of two electrons from the multiexciton (ME) state resulting from singlet fission. The efficiency of multielectron transfer is expected to depend critically on other dynamic processes available to the singlet (S-1) and the ME, but little is known about these competing channels. Here we apply time-resolved photoemission spectroscopy to the tetracene/C-60 interface to probe one- and two-electron transfer from S-1 and ME states, respectively. Unlike ultrafast (similar to 100 fs) singlet fission in pentacene where two-electron transfer from the multiexciton state resulting from singlet fission dominates, the relatively slow (similar to 7 ps) singlet fission in tetracene allows both one- and two-electron transfer from the Si and the ME states that are in a quantum mechanical superposition. We show evidence for the formation of two distinct charge transfer states due to electron transfer from photoexcited tetracene to the lowest unoccupied molecular orbital (LUMO) and the LUMO+1 levels in C-60, respectively. Kinetic analysis shows that similar to 60% of the S-1 double left right arrow ME quantum superposition transfers one electron through the S-1 state to C-60 while similar to 40% undergoes two-electron transfer through the ME state. We discuss design principles at donor/acceptor interfaces for optimal multiple carrier extraction from singlet fission for solar energy conversion.