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Unformatted text preview: mixture when using out Pasteur pipette. It was probably ethanol left on the crystals that had not completely evaporated. Despite the presence of impurities, our percent yield was suitable. Questions 1. Would it be possible to form 1,4-di-t-butyl-2,5-dimethoxybenzene by treating 1,4-dimethoxy benzene with a four carbon alkene and sulfuric acid? Show with mechanism, why you answered yes or no. 2. What would the product have been if cyclohexanol had been substituted for t-butyl alcohol? 1,4-dicyclohexanol-2,5-dimethoxybenzene. 3. What would the product of the reaction have been if 1,3-dimethoxybenzene had been substituted for 1,4-dimethoxybenzene? 1,5-di-t-butyl-2,4-dimethoxybenzene....
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This note was uploaded on 07/19/2009 for the course CHEM 234-54 taught by Professor Morrison during the Spring '09 term at University of Georgia Athens.
- Spring '09