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Isomer Definition

Isomers are molecules that have the same chemical formula but a different arrangement of atoms. There are several types of isomers, including structural isomers, stereoisomers, and enantiomers.

Isomer Definition

Structural isomers

Structural isomers, also known as constitutional isomers, have the same chemical formula but a different arrangement of atoms in the molecule. For example, butane and isobutane are structural isomers because they have the same chemical formula (C4H10) but a different arrangement of atoms. Butane has a linear structure, while isobutane has a branched structure.

Stereoisomers

Stereoisomers are isomers that have the same arrangement of atoms but a different spatial orientation of the atoms. There are two types of stereoisomers: geometric isomers and enantiomers.

  1. Geometric isomers: Geometric isomers have the same atoms and bonds, but the atoms are arranged in different orientations in space. A common example of geometric isomers is cis-trans isomers found in alkenes. Cis isomers have substituents on the same side of the double bond, while trans isomers have substituents on opposite sides of the double bond.
  2. Enantiomers: Enantiomers are stereoisomers that are mirror images of each other, but they are not superimposable. For example, the two enantiomers of a molecule of 2-butanol are mirror images of each other, but they are not superimposable. Enantiomers have opposite configurations at the chiral center and can have different physical and chemical properties, such as melting and boiling points, solubility, and reactivity.

Optical isomers

Enantiomers are a special type of stereoisomers that are mirror images of each other but not superimposable. They are also known as optical isomers. Enantiomers are non-superimposable mirror images of each other, which means that they are identical in every way except for the fact that they are mirror images. For example, the two enantiomers of a molecule of 2-butanol are mirror images of each other, but they are not superimposable.

They have opposite configurations at the chiral center and can have different physical and chemical properties, such as melting and boiling points, solubility, and reactivity. Enantiomers also have opposite optical rotation, which means that one enantiomer will rotate plane-polarized light clockwise, while the other enantiomer will rotate it counterclockwise. This property is used to differentiate and purify enantiomers in the field of chiral chemistry.

Isomer Definition

Constitutional isomers

Structural isomers, also known as constitutional isomers, have the same chemical formula but a different arrangement of atoms in the molecule. This means that they have the same number of atoms of each element, but they are bonded together in different ways. Structural isomers can be classified into several subcategories, including chain isomers, positional isomers, and functional group isomers.

  1. Chain isomers: Chain isomers have the same number of carbon atoms but different arrangements of these atoms in a chain.
  2. Positional isomers: Positional isomers have the same functional group but different positions of the atoms in a molecule.
  3. Functional group isomers: Functional group isomers have the same number of carbon atoms and the same functional groups, but the functional groups are in different positions in the molecule.

Conclusion

In conclusion, Isomers are molecules that have the same chemical formula but a different arrangement of atoms. Structural isomers have a different arrangement of atoms in the molecule, stereoisomers have the same arrangement of atoms but a different spatial orientation of the atoms and enantiomers are stereoisomers that are mirror images of each other, but they are not superimposable. Understanding these different types of isomers is important for understanding the properties and reactivity of different compounds.


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