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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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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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Esters, like aldehydes and ketones, are weakly acidic. When an ester with an alpha hydrogen is treated with one equivalent of a base such as sodium ethoxide, a reversible condensation reaction occurs to yield a β−keto ester product. This reaction between two ester components is known as the Claisen condensation reaction
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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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Carbonyl compounds are a broad group of compounds that includes aldehydes, ketones,carboxylic acids, and esters
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The reactivity of organometallic compounds increases with the percent ionic character of the carbon-metal bond. RLi and RMgX are of great importance in organic synthesis
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10.3 The Reactions of Alkanes with Halogens 10.3 A Multiple Substitution Reactions Versus Selectivity 10.4 Chlorination of Methane:Mechanism of Reaction
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Carboxylic acids are just one member of a class of acyl derivatives, RCOY, where the acyl group is bonded to an electronegatives substituent -Y that can act as a leaving group in substitution reactions. Numerous acyl derivatives are possible, but we’ll be concerned only with four of the more common ones, in addition to carboxylic acids themselves: acid halides, acid anhydrides, esters, and amides
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