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decided to carry out the synthesis using diethyl ether as the (Due to its low boiling point diethyl ether is a good, though highly flammable, bulk solvent for many organic reactions because it is readily removed from the reaction mixture.) She placed the appropriate mass of -butené in the diethyl ether solvent, then added MBr to start the reaction. She isolated a product and obtained a proton NMR spectrum for the sample. The spectrum that appeared on the screen was not the one the investigator was expecting. The following spectral data belong to the product obtained. integration singlet 1.84 quartet 1.75 2 triplet 0.903 Edit drawing I did not take the alkene pi-bond into consideration when planning this synthesis. O I forgot about the possibility of a carbocation rearrangement. O I must have used old diethyl ether that was contaminated with peroxides. 1 must not have waited long enough for the reaction to run to completion

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