A pulse radiolysis study of vitamin K-1 reduction was carried out in a
rgon-saturated ethanolic solutions. The alpha-hydroxyethyl radicals (C
H3CHOH)-H-. (R(.)) and the-solvated electrons, (e(solv)(-)) reduce vit
amin K-1, leading to the semiquinone transient K1H.. This species, cha
racterized by its absorption spectrum, decays by disproportionation an
d leads to the formation of the hydroquinone K1H2. The rate constants
of the monoelectronic exchanges involved in this reduction have been d
etermined.