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The most characteristic reactions of benzenoid arenes are the substitution reactions that occur when they react with electrophilic reagents. The electrophiles are either a positive ion (E+) or some other electron-deficient species with a large partial positive charge
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More reactive than benzene toward electrophilic substitution NO2 An deactivating group Less reactive than benzene toward electrophilic substitution Ortho-para director Meta director
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Aldehydes are named by replacing the terminal –e of the corresponding alkane name with –al. The longest chain selected as the base name must contain the –CHO group, and the –CHO carbon is always numbered as carbon 1
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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
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A ring that contains at least one heteroatom (an atom other than carbon) is called a heterocycle, and a substance based on a heterocyclic ring is a heterocyclic compound. Heterocyclic compounds containing N, O or S are by far the most common
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10.7 The Geometry of Alkyl Radicals 10.8 Reactions That Generate Tetrahedral Stereocenters 10.9 Radical Addition to Alkenes: TheAnti-Markovnikov Addition ofHydrogen Bromide
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7.3 芳香烃的化学性质 Reactions of Aromatic Hydrocarbons 7.4 苯环上亲电取代的定位规律 Orientation of Reactions on Substituted Aromatic Rings
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More environment-friendly methods Natural insect attractants — instead pesticide Less reactive compounds organic refrigerants and aerosol propellant — instead Freon (that destroy the Earth’s ozone layer) Cars with more efficient combustion engines — reduce the massive amount of automobile
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1.12A The Structure of Methane sp3 Hybridization The 4 sp3 orbitals should be oriented at angles of 109.5° with respect to each other. An sp3-Hybridized carbon gives a tetrahedral structure for methane, and with four equivalent C—H bonds
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