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Introduction to stereochemistryfor s...

Schmiermund, Torsten.

Introduction to stereochemistryfor students and trainees /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Introduction to stereochemistryby Torsten Schmiermund.
Reminder of title:	for students and trainees /
Author:	Schmiermund, Torsten.
Published:	Wiesbaden :Springer Fachmedien Wiesbaden :2021.
Description:	ix, 52 p. :ill., digital ;24 cm.
Contained By:	Springer Nature eBook
Subject:	Stereochemistry.
Online resource:	https://doi.org/10.1007/978-3-658-32035-5
ISBN:	9783658320355$q(electronic bk.)

Introduction to stereochemistryfor students and trainees /
Schmiermund, Torsten.

Introduction to stereochemistryfor students and trainees /[electronic resource] :by Torsten Schmiermund. - Wiesbaden :Springer Fachmedien Wiesbaden :2021. - ix, 52 p. :ill., digital ;24 cm. - essentials. - essentials..

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. This Springer essential is a translation of the original German 1st edition essentials, Einfuhrung in die Stereochemie 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. The content Introduction to the stereochemistry of organic compounds Differences between configuration, confirmation, constitution isomerism and tautomerism Distinction of geometric isomerism and mirror image isomerism Different display/visualization options for isomers Different display variants for sugar molecules The target groups Students of chemistry, pharmacy, medicine and biology Trainees in chemical professions (chemical laboratory assistants, CTA) The author Torsten Schmiermund has been working as a chemical engineer in the chemical industry for many years.

ISBN: 9783658320355$q(electronic bk.)

Standard No.: 10.1007/978-3-658-32035-5doiSubjects--Topical Terms:

194972
Stereochemistry.

LC Class. No.: QD481 / .S36 2021

Dewey Class. No.: 541.223

Introduction to stereochemistryfor students and trainees /
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520 $a 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. This Springer essential is a translation of the original German 1st edition essentials, Einfuhrung in die Stereochemie 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. The content Introduction to the stereochemistry of organic compounds Differences between configuration, confirmation, constitution isomerism and tautomerism Distinction of geometric isomerism and mirror image isomerism Different display/visualization options for isomers Different display variants for sugar molecules The target groups Students of chemistry, pharmacy, medicine and biology Trainees in chemical professions (chemical laboratory assistants, CTA) The author Torsten Schmiermund has been working as a chemical engineer in the chemical industry for many years.
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