You have the rate law
d[N2O5]/dt = -2 k [N2O5]n = K [N2O5]n
Now you may try different orders n until you fit to the data. For instance, n=0 means that v would be constant and your data shows that v is not constant; then cannot be n=0. Try n=1, n=2, n=3...
For instance, for n=1 one obtains, integrating the rate law,
ln[N2O5] = ln[N2O5]0 - Kt
this means that when you plot ln[N2O5] versus time you see a line with tangent -K if your reaction is first order.
For n=2 one obtains
1/[N2O5] = 1/[N2O5]0 + Kt
this means that when you plot 1/[N2O5] versus time you see a line with tangent K if your reaction is second order.
And so on.