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Lecture

Topic 2a Summary: "Alkanes & Cycloalkanes"

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Department
Biochemistry
Course Code
Biochemistry 2280A
Professor
Mel Usselman

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Organic Chemistry Key Concepts: Alkanes & Cycloalkanes (Usselman Version) -Straight or branched chain compounds of carbon and hydrogen are termed acyclic hydrocarbons or alkanes. Alkanes are unreactive as the electrons are perfectly balanced between the atoms and the carbon-carbon bonds are quite durable. All alkanes fit the general formula: C n 2n + 2 -Constitutional isomers are compounds that have the same molecular formula but different bonding sequences (properties). When drawing possible constitutional isomers, remember to concentrate on the C atom bonding sequence. -The “dot-line-wedge” is the most versatile, widely-used convention for the 3-dimensional drawing of molecules. Atoms in molecules always spin around σ bonds. Newman projections and Fischer projections are also used extensively. -Differing short-lived spatial arrangements of atoms, termed conformations, can result from the rapid rotation of atoms, or groups of atoms, about single bonds. Staggered conformations are of slightly lower energy than eclipsed ones. Conformations cannot normally be separated or isolated and are therefore not isomers. -Hydrocarbons closed to form a ring are known as cycloalkanes. Cycloalkanes fit the general formula CnH 2ncause two Hs have to be removed from an alkane to allow the ring to form. -The boat conformation of cyclohexane is present in the conformation equilibrium mixture in very small amounts. The chair
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