The excitation energy to the 2(1)A(g) state of trans-1,3-butadiene is examined using a variety of ab initio electronic structure techniques. While analogous states have been shown to be the lowest singlet excited states for all longer polyenes, for butadiene the position of the 2(1)A(g) state relative to the HOMO --> LUMO excitation (1(1)B(u)) has been difficult to establish theoretically. We employ a variety of methods (CASSCF, CASPT2, MRSDCI, QDVPT) to examine both the vertical and adiabatic excitation energies for this state. At the groundstate geometry, the vertical excitation energies obtained by CASPT2 and Davidson-corrected MRSDCI for the 2(1)A(g) state differ by approximately 0.15 eV, bur all of the methods predict that the 2(1)A(g) state has a lower 0-0 excitation energy than the 1(1)B(u) state. Possible reasons for the discrepancies between the various methods for the vertical excitation energy are discussed.