cis-trans isomerism
Spatial arrangement variation
Cis-trans isomerism is a type of stereoisomerism in chemistry where molecules have the same atoms and bonds but different spatial arrangements around a rigid structure, typically a double bond or ring.
In the cis form, similar groups lie on the same side; in the trans form, they're on opposite sides.
Cis-trans isomerism explains why some fats are solid and others liquid at room temperature.
Bonding hydrogen to compounds
- polymerizationMonomers bonding into chains
- margarineVegetable oil spread
- retinalOf eye's inner lining
- Ziegler-NattaCatalyst for ordered polymers
Spatially distinct molecular forms
- spatial arrangementPositioning of elements in space
- chiralityMirror-image non-superimposability
- enantiomersMirror-image molecular pairs
- racemic mixtureEqual parts both enantiomers
hydrogenation
Bonding hydrogen to compounds
- polymerizationMonomers bonding into chains
- margarineVegetable oil spread
- retinalOf eye's inner lining
stereoisomers
Spatially distinct molecular forms
- spatial arrangementPositioning of elements in space
- chiralityMirror-image non-superimposability
- enantiomersMirror-image molecular pairs
double bonds
Two shared electron pairs
- unsaturationHaving multiple bonds
chelation
Chemical metal-ion capture
- geometric isomers
- rearrangementsrearrangement, reshuffle, reorder, permutation, transpose
- Olefinationphosphonate