Experimentally, we know that the vapor pressure of the solvent above a solution containing a non-volatile solute (i.e., a solute that does not have a vapor pressure of its own) is directly proportional to the mole fraction of solvent in the solution. This behavior is summed up in Raoult's Law:
Psolvent=XsolventPsolvent∘
where:
Psolvent is the vapor pressure of the solvent above the solution,
Xsolvent is the mole fraction of the solvent in the solution,
Psolvent∘ is the vapor pressure of the pure solvent.
From reference data P0=0.6 kPa at 0 C
P must be 0.5 kPa, so X is next:
0.5=x×0.6x=0.8333, so
n of water =100/18=5.55 mol
n of urea =x/(5.55+x)=(1−0.8333)
x=1,11 mol
Mw of urea =60
m=n×Mw=60×1,11=6.66 g