Conformational

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Conformational isomerism is a form of Stereoisomerism in Chemistry that describes the phenomenon of molecules with the same structural formula but with different arrangements of atoms in space. This is due to the rotation about single bonds, and it is particularly relevant in the case of Organic compounds.

Overview[edit | edit source]

Conformational isomerism involves a change in the shape of a molecule resulting from a rotation about a single bond. This type of isomerism is only possible in molecules that have a single bond. The different shapes that these molecules can adopt are called conformations.

Types of Conformational Isomerism[edit | edit source]

There are two main types of conformational isomerism: Eclipsed Conformation and Staggered Conformation.

Eclipsed Conformation[edit | edit source]

In an eclipsed conformation, the atoms or groups of atoms attached to the carbon atoms are as close together as possible. This results in a higher energy state due to Steric hindrance.

Staggered Conformation[edit | edit source]

In a staggered conformation, the atoms or groups of atoms attached to the carbon atoms are as far apart as possible. This results in a lower energy state.

Factors Affecting Conformational Isomerism[edit | edit source]

Several factors can affect conformational isomerism, including the size of the atoms or groups of atoms attached to the carbon atoms, the presence of double bonds or triple bonds, and the temperature.

Applications[edit | edit source]

Conformational isomerism has important implications in the fields of Organic chemistry, Biochemistry, and Pharmaceutical chemistry. It can affect the physical and chemical properties of molecules, their reactivity, and their biological activity.

Conformational Resources
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Contributors: Prab R. Tumpati, MD