Answer:
a) Watch the attaccment
b) Ethyl bromide is more reactive than n-propyl bromid, and this more than neopentyl bromide. Ethyl bromide has less steric hindrance than the others, to SN2 reactions.
c) t-butyl bromide is more reactive than isopropyl bromide, and this more than ethyl bromide. t-butyl bromide structure stabilize the carbocation, better than the others.
Explanation:
Speed of SN2 reactions depends on steric hindrance, the less hindrance, the most reaction speed, meaning more reactivity. Then, those linear structures are more reactive to SN2 reactions.
In the other hand, speed of SN1 reactions depends on the stability of the carbocation formed. Structure with ramifications can stabilize better the carbocation, these structures are more reactive to SN1 reactions.
