A compound has the molecular formula C4H8O and contains a carbonyl group. Identify the compound on the basis of its 1H NMR spectrum shown in Figure 17.17.
Answer to relevant QuestionsA compound (C7H14O) has a strong peak in its infrared spectrum at 1710 cm-1. Its 1H NMR spectrum consists of three singlets in the ratio 9:3:2 at δ 1.0, 2.1, and 2.3 ppm, respectively. Identify the compound.Give an acceptable alkylamine or alkanamine name for each of the following amines:Each of the following is a much weaker base than aniline. Present a resonance argument to explain the effect of the substituent in each case.Nitrous acid deamination of 2, 2-dimethylpropylamine, (CH3)3CCH2NH2, gives the same products as were indicated as being formed from 1, 1-dimethylpropylamine in Figure 22.5. Suggest a mechanism for the formation of these ...Arrange the following compounds or anions in each group in order of decreasing basicity: (a) H3C-, H2N-, HO-, F- (b) H2O, NH3, HO-, H2N- (c) HO-, H2N-, C N, NO3
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