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    <subfield code="a">Pattaraporn Posoknistakul</subfield>
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    <subfield code="a">In  this  research,  the  lignin  reactivity  during  alkaline delignification  was  quantitatively investigated  focusing  on  the  effect  of  the  structural  differences  between  syringyl  and guaiacyl  aromatics  nuclei  as  well  as  various  alkaline  conditions  on  the&#xDD;-O-4 bond cleavage rate.Moreover, the lignin compounds with 2-carbon side chains were studied to avoid  the  complex  kinetics  caused  by  the  propanol  diastereomers  which  hydrolyze  at different rates and the &#xDC;{u2013}and &#xDE;{u2013}hydroxyls both participating in the displacement reaction.The presence of a syringyl nucleus, increasing of the reaction temperature as well as higher alkaline concentration influenced the increasing of the reaction rate.</subfield>
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