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SOLVED: Bromination of 3-methyl-2-butanone yielded two compounds, each having the molecular formula C4H9Br, in a 95.5 ratio. The H-NMR spectrum of the major isomer was characterized by a doublet at δ 1.2 (6H). The H-NMR spectrum of the minor isomer B exhibited two singlets, one at δ 1.9 and the other at δ 2.5. The lower-field singlet had half the area of the higher-field singlet. Select the structures for these two products:A. 1-bromo-3-methyl-2-butanoneB. 4-bromo-3-methyl-2-butanoneC. A = 1-
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