Organic chem unit 30 - isomers

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20 Terms

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Isomerism

The presence of different compounds with the same molecular formula but different arrangement of atoms

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The two types of isomerism are structural and __

stereoisomerism

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Stereoisomerism

Different arrangement in space in each isomer of the same atoms that are bonded together in the same order

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Cis-trans-isomerism

Caused by restricted rotation around the C=C double bond

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Cis isomer

Isomer of a carbon compound containing a C=C double bond with 2 of the same (groups of) atoms on the same side of the double bond

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Trans isomer

Isomer of a carbon compound with a C=C double bond where 2 of the same (group of) atoms are on opposite sides of the double bond

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Structural isomerism

The same atoms that are bonded together in a different order in each isomer

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<p>Chain isomers</p>

Chain isomers

Carbon compounds with the same molecular formula that differ in lengths of carbon chain due to the possibility of branching

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<p>Position isomers</p>

Position isomers

Carbon compounds with the same molecular formula but different positions of the same functional group(s) on the carbon chain

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Functional group isomerism

Carbon compounds with the same molecular formula but different functional groups

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<p>Enantiomerism</p>

Enantiomerism

Isomers that contain chiral carbon centres bonded to 4 different groups or atoms (in a tetrahedral arrangement)

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Chirality

The presence of mirror images of a compound that are non-superimposable upon each other

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Plane of polarisation

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Optical activity

The ability of a chemical species to rotate a plane-polarised plane of polarised light

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Explain the differences in physical properties between butan-1-ol and 2-methylpropan-1-ol in terms of structure.

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Explain the differences in physical properties between butan-1-ol and butan-2-ol in terms of structure.

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How do the chemical properties of cis-trans isomers differ?

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How do the physical properties of cis-trans isomers differ?

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Explain the differences in boiling point between cis-but-2-ene and trans-but-2-ene.

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Explain the differences in optical activity in these two stereoisomers.