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Stereoisomers are compounds with the same chemical formula and connectivity but with different arrangements of their atoms in 3-dimensional space. Stereochemistry encompasses the study of stereoisomers and their properties. Despite having an identical chemical formula, stereoisomers can have drastically different biological, medicinal, and chemical properties. Basic Organic Stereochemistry explains in clear, concise terms the concepts and properties of stereoisomers. Ideal both as a text for advanced undergraduate or graduate students and as a handy guide for researchers in industry, this superb text covers: Polarimetry and optical rotation Internal coordinates, configuration, and conformation Nature of stereoisomers Barriers between stereoisomers and residual stereoisomers Symmetry operators and symmetry point groups Properties of stereoisomers and stereoisomer discrimination Separation of stereoisomers, resolution, and racemization Suitable for students in organic and biological chemistry, Basic Organic Stereochemistry is unparalleled as a convenient text.
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Awarded the first Nobel Prize in Chemistry in 1901 for his work on chemical dynamics and on osmotic pressure in solutions, the Dutch scientist Jacobus Henricus van 't Hoff (1852-1911) was also a pioneer in the field of stereochemistry - the three-dimensional analysis of chemical structures. This 1898 publication is based on the revised and expanded German translation of his Dix années dans l'histoire d'une théorie (1887), itself an updated version of his major work La chimie dans l'espace (1875). Translated and edited by the English chemist Arnold Eiloart, it covers the stereochemistry of carbon and nitrogen compounds, and contains an appendix on inorganic compounds by the Swiss chemist Alfred Werner (another future recipient of the Nobel Prize in Chemistry). Using experimental results, van 't Hoff shows how the varying spatial arrangement of similar compounds leads to differing chemical and optical behaviour.
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