Answer:
Ether
SN1 mechanism
Explanation:
The nucleophile in this reaction is CH3OH. It is a poor nucleopile. We already know that a poor nucleophile reacting with a tertiary alkyl halide often leads to the substitution product as the major product.
Also, the iodide ion is a good leaving group. This makes the SN1 substitution more likely yielding the ether as the major product as shown in the image attached.
