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-Has asymmetric center(s) -Achiral -Optically inactive -Plane of Symmetry, no enantiomers |
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When 2 constitutional isomers can be obtained as products, but more of ONE is created than the other. |
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Preferential formation of a stereoisomer rather than a constitutional isomer |
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Each stereoisomer forms a different stereoisomeric product/set of stereoisomeric producs. |
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When 2 substituents add to the SAME side of a double bond. |
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When 2 substituents add to OPPOSITE sides of a double bond. |
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Hydrocarbon with a carbon-carbon TRIPLE bond. -4 fewer hydrogens than an alkane. |
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Molecular formula for an ALKANE |
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Molecular formula for ACYCLIC ALKYNE |
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Molecular formula for CYCLIC ALKYNE |
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Triple bond is at the end of the chain. |
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Triple bonds located anywhere but the ends of the carbon chain. |
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Compound with 2 TRIPLE bonds |
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Compound with 2 DOUBLE bonds |
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A molecule with 2 halogens on the same carbon |
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Halogens Cl2 and Br2 add to alkynes. With excess halogen, a 2nd addition rxn occurs. WITH THIS SOLVENT... |
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Compound with a carbon-carbon double bond and an OH group bonded to one of the sp2 carbons |
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