Chapter 23
Organic Chemistry
By Boundless
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Alkanes are relatively unreactive hydrocarbons that contain no double or triple bonds in their carbon skeletons.
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Alkanes are generally unreactive, but can participate in oxidation, halogenation, and cracking reactions.
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Hydrocarbon structures can be drawn from the IUPAC names of chemical compounds by starting with the carbon backbone and adding substituents.
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Cycloalkanes are saturated hydrocarbons that contain a ring in their carbon backbones.
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Alkenes and alkynes are named similarly to alkanes, based on the longest chain that contains the double or triple bond.
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Due to the presence of a double bond in their carbon skeletons, alkenes are more reactive than their related alkanes.
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Alkenes and alkynes are more reactive than alkanes due to their pi bonds.
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Aromatic compounds are named based on the number and type of substituents on the ring.
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Aromatic compounds are ring structures with delocalized
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Aromatic compounds can participate in a range of reactions including substitution, coupling, and hydrogenation reactions.
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Functional groups refer to specific atoms bonded in a certain arrangement that give a compound certain physical and chemical properties.
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Alcohols are functional groups characterized by the presence of an -OH group.
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Ethers are a class of organic compounds characterized by an oxygen atom connected to two alkyl or aryl groups.
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Aldehydes and ketones are classes of organic compounds that contain a carbonyl (C=O) group.
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Carboxylic acids are organic acids that contain a carbon atom that participates in both a hydroxyl and a carbonyl functional group.
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Esters are functional groups produced from the condensation of an alcohol with a carboxylic acid, and are named based on these components.
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Amines are compounds characterized by the presence of a nitrogen atom, a lone pair of electrons, and three substituents.