In chemistry, cis-trans isomerism or geometric isomerism or configuration isomerism is a form of stereoisomerism describing the orientation of functional groups within a molecule. In general, such isomers contain double bonds, which cannot rotate, but they can also arise from ring structures, wherein the rotation of bonds is greatly restricted.
The term "geometric isomerism" is considered an obsolete synonym of "cis-trans isomerism" by IUPAC. It is sometimes used as a synonym for general stereoisomerism (e.g., optical isomerism being called geometric isomerism); the correct term for non-optical stereoisomerism is diastereomerism.
There are two forms of a cis-trans isomer, the cis and trans versions. When the substituent groups are oriented in the same direction, the diastereomer is referred to as cis, whereas, when the substituents are oriented in opposing directions, the diastereomer is referred to as trans. An example of a small hydrocarbon displaying cis-trans isomerism is 2-butene.
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In chemistry, cis-trans isomerism or geometric isomerism or configuration isomerism is a form of stereoisomerism describing the orientation of functional groups within a molecule. In general, such isomers contain double bonds, which cannot rotate, but they can also arise from ring structures, wherein the rotation of bonds is greatly restricted.
The term "geometric isomerism" is considered an obsolete synonym of "cis-trans isomerism" by IUPAC. It is sometimes used as a synonym for general stereoisomerism (e.g., optical isomerism being called geometric isomerism); the correct term for non-optical stereoisomerism is diastereomerism.
There are two forms of a cis-trans isomer, the cis and trans versions. When the substituent groups are oriented in the same direction, the diastereomer is referred to as cis, whereas, when the substituents are oriented in opposing directions, the diastereomer is referred to as trans. An example of a small hydrocarbon displaying cis-trans isomerism is 2-butene.
from wiki