Answer:
The most consistent mechanism is SN1.
Explanation:
The solvolysis of tert-butyl iodide in methanol will arise by the SN1 mechanism.
The reason for that is due the geometric structure of tert-butyl. The tertiary structure allows the formation of a stable carbocation, after the loss of the iodide ion. The carbocation will then be attacked by methanol molecules forming an eter.
I can’t answer the exact thing, but I know how to do it. One of the nitrogen bases always pairs with a different one, so once you know what pairs with what you just write it down. If you need more help just ask :) tip: one base will only join with a different one. One won’t join to multiple (from what I know as of now)
