The Auger electron spectrum associated with decay of a core-hole on th
e terminal nitrogen and that associated with the central nitrogen of n
itrous oxide, N2O, are obtained individually through the use of a coin
cidence technique. Specifically, each of the two Auger electron spectr
a is obtained by detection of Auger electrons in coincidence with near
zero energy (threshold) photoelectrons at the respective ionization t
hresholds. These zero energy electrons serve to identify the core-ioni
zation continuum associated with the different Auger electrons. The sa
lient features of the experimental spectra are in good agreement with
theoretical calculations. The low counting rate generally associated w
ith coincidence experiments, especially in the gas phase, is not encou
ntered because the low energy electrons are collected over a 4pi solid
angle. Also, velocity discrimination is accomplished by a spatial fil
ter rather than by time-of-flight to utilize the maximum duty cycle of
the synchrotron source. These data are believed to be the first examp
les of chemical-site-selective molecular Auger spectra.