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Flashcards covering the fundamentals of organic chemistry, including nomenclature, functional groups, and chemical reactions of hydrocarbons and their derivatives.
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Organic Chemistry
The chemistry of carbon compounds which includes several million known compounds from nature and synthetic sources.
Functional group
A reactive portion of the molecule that undergoes predictable reaction.
Bonding unit: Hydrogen
Consists of 1 bond and no lone pairs.
Bonding unit: Oxygen
Consists of 2 bonds and 2 lone pairs.
Bonding unit: Carbon
Consists of 4 bonds and no lone pairs.
Bonding unit: Nitrogen
Consists of 3 bonds and 1 lone pair.
Bonding unit: Halogens
Consist of 1 bond and 3 lone pairs.
Tetrahedral geometry
Configuration around a carbon atom with a bond angle of 109.5∘.
Trigonal geometry
Configuration around a carbon atom with a bond angle of 120∘.
Linear geometry
Configuration around a carbon atom with a bond angle of 180∘.
Isomers
Compounds having the same molecular formula but differing in structural formulas.
Saturated Hydrocarbons
Compounds containing only C and H-atoms where all the C-atoms are sp3 hybridized; examples include Alkanes and Cycloalkanes.
Homologous series
A collection of organic compounds which differ in structure by a −CH2− (methylene) group, contain the same functional group, and can be represented by the same general formula.
Alkanes
Saturated hydrocarbons with the general formula CnH2n+2.
Cycloalkanes
Saturated hydrocarbons with the general formula CnH2n.
Alkyl group (R)
A substituent formed by removing one hydrogen from an alkane chain, such as methyl (CH3) or ethyl (CH3CH2).
Alkenes (olefins)
Unsaturated hydrocarbons containing carbon-carbon double bonds (C=C) with the general formula CnH2n.
Geometric isomers
Atoms joined in the same way but occupying different relative positions in space due to a lack of rotation about a double bond (e.g., cis-2-butene and trans-2-butene).
Markovnikov's rule
States that in the addition of unsymmetrical addenda to unsymmetrical alkenes, the hydrogen atom of the addendum adds to the alkenic C-atom with the more H-atoms.
Alkynes
Straight chain acyclic hydrocarbons containing a triple bond (C≡C) with the general formula CnH2n−2.
Arene
The generic name for aromatic hydrocarbons, of which Benzene (C6H6) is the parent.
Heterolysis
The breaking of a covalent bond in such a way that both the bonding electrons go to one of the bonded atoms, forming a reactive carbocation (R+) and a weak base (X−).
Alcohols
Organic compounds containing a hydroxyl group (−OH) on a saturated carbon atom; general formula R−OH.
Phenols
Aromatic alcohols where the hydroxyl group (−OH) is directly attached to an arene ring.
Ethers (Alkoxyalkanes)
Non-polar, volatile organic compounds with the general formula R−O−R (symmetrical) or R−O−R1 (unsymmetrical).
Carbonyl group
A highly reactive functional group consisting of a carbon atom double-bonded to an oxygen atom (C=O).
Aldehydes (Alkanals)
Carbonyl compounds where the carbon is bonded to at least one hydrogen; general formula R−CHO.
Ketones (Alkanones)
Carbonyl compounds where the carbon is bonded to two alkyl or aryl groups; general formula R−COR′.
Tollen's test
A 'silver mirror test' used to distinguish aldehydes from ketones by reducing Ag+/NH4+ to metallic silver.
Carboxylic acids (Alkanoic acids)
Organic acids containing the carboxyl group (−COOH) with the general formula R−COOH.
Esterification
The reaction of a carboxylic acid with an alcohol in the presence of an acid catalyst to form an ester and water.
Saponification
Alkaline hydrolysis of an ester using a base like NaOH to form a soap (carboxylic acid salt) and an alcohol.
Amides
Derivatives of alkanoic acids with the general formula R−CONH2; they are the least reactive derivatives because the −NH2 group is a poor leaving group.
Amines
Organic relatives of ammonia (NH3) where one or more hydrogens are replaced by hydrocarbon groups; categorized as primary (1∘), secondary (2∘), or tertiary (3∘).