Here you have to keep in mind some facts . Firstly , primary alkyl halides readily go for sn2
CH3X > C2H5X and so on
Secondary alkyl halides go for sn2 at slower rate than sn1 .Also, in this case solvent matters , in case of polar protic solvent they go for sn1 rather than sn2.
Tertiary does not go for sn2 rather it goes for sn1.
Remember for sn2 i)more +ve charge density and ii) less hinderance is favourable.
For sn1 rate is proportional to the carbocation stability. More stable carbocation faster rate.
Approve the answer if correct.