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According to Wikipedia, an E2 reaction is typically of secondary and tertiary substituted alkyl halides. An E2 reaction results in formation of a Pi bond. The reason we only used an E1 reaction is because the alcohol functional group was attached to a tertiary carbon, which makes it very compatible to have the compound go through an E1 reaction. In addition, we were using sulphuric acid with heat, it is considered as a weak base making the reactivity for an E1 reaction strong. The reaction also would favor a protic solvent in order for it to be an E1 reaction. When the compound goes through the E1 reaction, it forms a carbocation, and in some cases it could be formed on a secondary carbon...
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