Most delignification in sulfite pulping involves acidic cleavage of ether bonds, which connect many of the constituents of lignin.[2] Theelectrophiliccarbocations produced during ether cleavage react with bisulfite ions (HSO3−) to give sulfonates.
R-O-R' + H+ → R+ + R'OH
R+ + HSO3− → R-SO3H
The primary site for ether cleavage is the α-carbon (carbon atom attached to the aromatic ring) of the propyl (linear three carbon) side chain. The following structures do not specify the structure since lignin and its derivatives are complex mixtures: the purpose is to give a general idea of the structure of lignosulfonates. The groups R1 and R2 can be a wide variety of groups found in the structure of lignin. Sulfonation occurs on the side chains, not on the aromatic rings, like in p-toluenesulfonic acid.