Details

Introduction to Stereochemistry


Introduction to Stereochemistry

For Students and Trainees
essentials

von: Torsten Schmiermund

CHF 27.50

Verlag: Springer
Format: PDF
Veröffentl.: 07.06.2021
ISBN/EAN: 9783658320355
Sprache: englisch

Dieses eBook enthält ein Wasserzeichen.

Beschreibungen

<p>Conformal, diastereomers, rotamers, tautomers, anomers: The multitude of terms used in stereochemistry quickly makes this subfield of chemistry confusing. In addition, there are different nomenclatures and different forms of representation (Fischer projection, Haworth ring formula, Newman projection). This essential deals with basic static stereochemistry and gives an overview of the different isomeric forms and nomenclatures. It is thus both a help and a reference book.&nbsp;&nbsp;<br></p><p>This <i>Springer essential</i> is a translation of the original German 1st edition <i>essentials</i>,&nbsp;<i>Einführung in die Stereochemie</i>&nbsp;by Torsten Schmiermund, published by Springer Fachmedien Wiesbaden GmbH, part of Springer Nature in 2019. The translation was done with the help of artificial intelligence (machine translation by the service DeepL.com). A subsequent human revision was done primarily in terms of content, so that the book will read stylistically differently from a conventional translation. Springer Nature works continuously to further the development of tools for the production of books and on the related technologies to support the authors.</p><div><br></div>
Introduction to the stereochemistry of organic compounds- Differences between configuration- Confirmation-, constitution-isomerism and tautomerism- Differentiation of geometric isomerism and mirror-image isomerism- Different display/visualization possibilities for isomers - Different display variants for sugar molecules<br>
<p>Torsten Schmiermund ist als Chemotechniker seit vielen Jahren in der chemischen IndustTorsten Schmiermund has been working as a chemical engineer in the chemical industry for many years.&nbsp;rie tätig.&nbsp;</p>
<p>Conformal, diastereomers, rotamers, tautomers, anomers: The multitude of terms used in stereochemistry quickly makes this subfield of chemistry confusing. In addition, there are different nomenclatures and different forms of representation (Fischer projection, Haworth ring formula, Newman projection). This essential deals with basic static stereochemistry and gives an overview of the different isomeric forms and nomenclatures. It is thus both a help and a reference book.&nbsp;</p><p>This <i>Springer essential</i> is a translation of the original German 1st edition <i>essentials</i>,&nbsp;<i>Einführung in die Stereochemie&nbsp;</i>by Torsten Schmiermund, published by Springer Fachmedien Wiesbaden GmbH, part of Springer Nature in 2019. The translation was done with the help of artificial intelligence (machine translation by the service DeepL.com). A subsequent human revision was done primarily in terms of content, so that the book will read stylistically differently from a conventional translation. Springer Nature works continuously to further the development of tools for the production of books and on the related technologies to support the authors.</p><div><b>The content</b><br></div><p></p><ul><li>Introduction to the stereochemistry of organic compounds</li><li>Differences between configuration, confirmation, constitution isomerism and tautomerism</li><li>Distinction of geometric isomerism and mirror image isomerism</li><li>Different display/visualization options for isomers</li><li>Different display variants for sugar molecules</li></ul><p></p><p><b>The target groups</b></p><p>Students of chemistry, pharmacy, medicine and biology<br></p><p></p><p>Trainees in chemical professions (chemical laboratory assistants, CTA)</p><p><b>The author</b></p><p>Torsten Schmiermund has been working as a chemical engineer in the chemical industry for many years.&nbsp;</p><p><br></p>
Quick and easy to understand introduction to the complex field of stereochemistry Suitable for first-year students and trainees alike Practical guide for quick orientation

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