Phenols are like alcohols in being able to form strong intermolecular hydrogen bonds. Phenols have higher boiling points than hydrocarbons of the same molecular weight. A modest solubility in water
More reactive than benzene toward electrophilic substitution NO2 An deactivating group Less reactive than benzene toward electrophilic substitution Ortho-para director Meta director
Compounds were classified as being either aliphatic or aromatic in the latter part of the nineteenth century. To be classified as aliphatic meant then that the chemical behavior of a compound was “fatlike”. To be classified as aromatic meant then that the compound had a low hydrogen/carbon ratio and that it was “fragrant
Conjugated unsaturated systems have a p orbital on a carbon adjacent to a double bond The p orbital can come from another double or triple bond The p orbital may be the empty p orbital of a carbocation or a p orbital with a single electron in it (a radical)
10.3 The Reactions of Alkanes with Halogens 10.3 A Multiple Substitution Reactions Versus Selectivity 10.4 Chlorination of Methane:Mechanism of Reaction
7.1 芳香烃的分类 结构及命名 Classification, Structures and Nomenclature of Aromatic Compounds 7.2 芳香烃的来源及物理性质 Sources and Physical Properties of Aromatic Hydrocarbons
4.1 卤代烃的分类 结构和命名 Classification, Structure, and Nomenclature of Alkyl Halides 4.2 卤代烃的物理性质 Physical Properties of Alkyl Halides 4.3 卤代烃的化学性质 Chemical properties of Alkyl Halides
