Answer
The resulting products are 1-(ethoxymethyl)cyclohex-1-ene and 1-ethoxy-2-methylenecyclohexane.
Work Step by Step
First, the given reactant undergoes a first-order ionization which leads to the formation of a resonance-stabilized carbocation. As the resulting carbocation is asymmetric, two products can be obtained via EtOH attack to it: 1-(ethoxymethyl)cyclohex-1-ene and 1-ethoxy-2-methylenecyclohexane.
