2. The SN1 reaction shown below is unusual in that the intermediate carbocation is not used up as fast as it is produced and accumulates in the reaction mixture (the carbocation turns out to be colored, providing a red-orange solution in the 2,2,2-trifluoroethanol used as solvent). One of the reasons that the carbocation intermediate is consumed relatively slowly is that it is quite stable (for a carbocation). Draw the carbocation intermediate and use further pictures to explain clearly its unusual stability. It turns out that the methoxy (OMe) substituents on the benzene rings are crucial, so be sure your explanation includes their role. Also, show how the final product is formed from the carbocation. Red-orange carbocation intermediate accumulates