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An acid is a substance that can donate (or lose) a proton, A base is a substance that can accept (or remove) a proton
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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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Functional groups The structural features that make it possible to classify compounds by reactivity are called functional groups. A functional group is a part of a larger molecule and is composed of an atom or a group of atoms that have a characteristic chemical behavior. The Chemistry of every organic molecules
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Carbon’s ability to form strong covalent bonds to other carbon atoms is the single property of the carbon atom that — more than any other—accounts for the existence of a field of study called organic chemistry. Carbon’s ability to form as many as four strong bonds to other carbon atoms, and to form strong bonds to hydrogen, oxygen, sulfur, and nitrogen atoms as well
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Quinones are an interesting and valuable class of compounds because of their oxidation-reduction, or redox, properties. The redox properties of quinones are important to the functioning of living cells, where compounds called ubiquinones(泛醌) act as biochemical oxidizing agents to mediate the electro-transfer processes involved in energy production
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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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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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The C—X bond of alkyl halides is polarized. The carbon atom bears a partial positive charge, The halogen atom a partial negative charge
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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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