
Why is it that the major product formed is through an Sn1 mechanism rather than an E1 mechanism?
I thought that if the reaction took place in increased temperature (the delta symbol means increased temperature right?), it would favor elimination rather than substitution, plus doesn't that Sn1 reaction have a lot of steric hindrance from the ethyl group which would slow down the rate of Sn1 and cause Elimination over substitution.
Furthermore, one particular elimination product can be formed by either the non-rearranged or rearranged carbocation.