Basics of Organic Chemistry: A Textbook for Undergraduate Students

Stereochemistry of Organic Compounds-II

Author(s): Anshul Bansal * .

Pp: 223-275 (53)

DOI: 10.2174/9789815223224124010007

* (Excluding Mailing and Handling)

Abstract

This chapter continues the exploration of stereochemistry in organic compounds, focusing on detailed methods for describing and differentiating the spatial arrangement of atoms within molecules. It begins with absolute configuration, which provides a precise description of the spatial arrangement of atoms around a chiral center, independent of other molecules.

Relative configuration is then discussed, explaining how the arrangement of atoms in one chiral molecule relates to another, often determined through chemical interconversion. The D-L system, a traditional method for denoting configurations based on the molecule’s relationship to glyceraldehyde, is introduced for historical context and specific applications.

The R-S system, the modern and widely used method for assigning absolute configuration based on the Cahn-Ingold-Prelog priority rules, is detailed, providing a systematic approach for designating chiral centers. Geometrical isomerism is explored next, focusing on compounds with restricted rotation around double bonds or ring structures, resulting in distinct cis-trans configurations.

The E-Z system, an advanced method for designating geometrical isomers based on the CahnIngold-Prelog priority rules, is introduced, offering a more precise description for complex molecules. Conformational isomerism, which arises from the rotation around single bonds, is then examined, highlighting its significance in the dynamic behavior of molecules.

Various conformations, particularly those of cycloalkanes and acyclic compounds, are analyzed, discussing the energy differences and interconversions between different conformers. Special attention is given to the impact of conformational isomerism on chemical reactivity and physical properties.

This chapter provides a deep understanding of the nomenclature and principles used to describe the three-dimensional arrangements of atoms in organic molecules, building on the foundations laid in the previous chapter. Mastery of these concepts prepares readers to analyze and predict the behavior of complex organic systems, essential for advanced studies and practical applications in organic chemistry. 


Keywords: Absolute configuration; relative configuration; D-L system; R-S system; geometrical isomerism; E-Z system; conformational isomerism; conformations.

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