Structural isomers

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Structural Isomers are a type of isomer where the atoms in a molecule are arranged in different ways, while maintaining the same molecular formula. This concept is a fundamental aspect of organic chemistry, and it plays a significant role in the diversity of organic compounds.

Overview[edit | edit source]

Structural isomers, also known as constitutional isomers, are unique forms of a single compound that differ in the arrangement of their atoms. The atoms are connected in a different order, resulting in different physical and chemical properties. This is in contrast to stereoisomers, where the atoms are connected in the same order but differ in spatial orientation.

Types of Structural Isomers[edit | edit source]

There are three main types of structural isomers: chain isomers, functional group isomers, and tautomers.

Chain Isomers[edit | edit source]

Chain isomers occur when the carbon skeleton of the molecule is rearranged. This can result in different types of chains, such as straight chains, branched chains, or rings.

Functional Group Isomers[edit | edit source]

Functional group isomers occur when the functional group of the molecule changes. For example, an alcohol could become an ether, or an aldehyde could become a ketone.

Tautomers[edit | edit source]

Tautomers are a special type of functional group isomer where the functional group changes location within the molecule. This often involves the movement of a hydrogen atom and a double bond.

Importance in Organic Chemistry[edit | edit source]

Structural isomers are crucial in organic chemistry because they allow for a vast number of possible compounds with the same molecular formula. This diversity is a key factor in the complexity and richness of organic chemistry.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD