What is the Difference Between Cis and Trans Isomers?
🆚 Go to Comparative Table 🆚Cis and trans isomers are types of geometric isomers that have the same molecular formula and weight, but they differ in the arrangement of atoms, particularly around a double bond. The main differences between cis and trans isomers are:
- Atomic arrangement: In cis isomers, two similar atoms or groups of atoms lie on the same side of a double bond, while in trans isomers, they lie on opposite sides of a double bond.
- Physical properties: Cis isomers usually have higher melting points than trans isomers due to stronger intermolecular forces of attraction. Trans isomers have comparatively lower boiling points because they lack strong attractive forces. Cis isomers are more soluble in polar solvents, whereas trans isomers have smaller solubility in neutral solvents.
- Acidity: Both forms of isomers have higher acid power, but the protons in trans isomers are not readily emitted, making them less acidic.
For example, consider the molecule but-2-ene. In the cis isomer, both methyl groups are on the same side of the double bond, while in the trans isomer, the methyl groups are on opposite sides of the double bond. The different arrangements of atoms in cis and trans isomers can lead to variations in their physical and chemical properties.
Comparative Table: Cis vs Trans Isomers
Cis and trans isomers, also known as geometric isomers, exist when there is restricted rotation in a molecule and there are two non-identical groups on each doubly bonded carbon atom. The difference between cis and trans isomers lies in the position of the substituents in the molecule. Here is a summary of their differences:
Cis Isomers | Trans Isomers |
---|---|
Substituents are on the same side of the carbon-to-carbon double bond | Substituents are on opposite sides of the carbon-to-carbon double bond |
Found in alkenes with one non-hydrogen group attached to each carbon of the C=C bond | More common in alkanes |
Structures are described using cis/trans nomenclature | Structures are described using E-Z notation for more complex cases |
For example, consider the molecule 1,2-dibromocyclopentane. It can exist as two different stereoisomers: cis-1,2-dibromocyclopentane and trans-1,2-dibromocyclopentane. The cis isomer has both bromine atoms on the same side of the ring, while the trans isomer has the bromine atoms on opposite sides.
- Isotopes vs Isomers
- Cis vs Trans Cyclohexane
- Structural Isomers vs Stereoisomers
- Congener vs Isomer
- Diastereomers vs Enantiomers
- E vs Z Isomers
- Constitutional Isomers vs Stereoisomers
- Geometric Isomers vs Structural Isomers
- Allotrope vs Isomer
- Cis vs Trans Stilbene
- Isomerization vs Hydroisomerization
- Chain Isomerism vs Position Isomerism
- Cis vs Trans Fat
- Cis vs Trans Fatty Acids
- Isomers vs Resonance
- Position Isomerism vs Metamerism
- Cis vs Trans Splicing
- Cisgenesis vs Transgenesis
- Isoschizomers vs Isocaudomers