@ joseph
1- increasing substitution increaseas stability
we look at the no. of bonding electrons that are attached to carbocation beacuse those bonding electrons , will help in allivating the +ve charge .
bonding electron from adjacent sigma bond may overlap with the unoccupied p orbital of the carbocation .
this is what we called hyperconjugation .
since the overlap supplies electron density to the electron deficient carbocation carbon , we predict the increasing number of hyperconjugative interactions increase carbocation stability .
increasing the no of bonds adjacent to carbocation by increasing the no. of alkyl group , attached to carbocation carbon result in increasing the stability .
thatswhy tertiary should be more stable than secondary .
so, primary
BUT this case might vary case by case ,
if u have any kind of exception example then u can ask , i will give the reason
all the best