According to Saytzeff rule, any alkyl halide that gives a more highly substituted (more stable) alkene undergoes dehydrohalogenation faster than the one which gives a less highly substituted (less stable) alkene. Thus, the ease of dehydrohalogenation of different alkyl halides having the same halogen decreases in the order
tertiary $\left(3^{\circ}\right)>$ secondary $\left(2^{\circ}\right)>$ primary $\left(1^{\circ}\right)$