Arrange the following in order of their increasing reactivity towards SN2 substitution reactions: bromomethane, 1-bromo-propane, 2-bromopropane, 2- bormo-2-methyl propane. Justify your answer.

SN2 (bimolecular nucleophilic substitution) reactions follow a single-step mechanism in which the nucleophile attacks the substrate from the opposite side of the leaving group, leading to a transition state and inversion of configuration. The rate of SN2 reactions is __________ _____ ___ _________ _____ _______ ____ ____.
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