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  2. Template:McMurry3rd - Wikipedia

    en.wikipedia.org/wiki/Template:McMurry3rd

    McMurry3rd is for referencing the 3rd edition (1992) of Organic Chemistry by John E. McMurry. It is based on the template {}. Parameters are: page (optional): to reference a single page; pages (optional): to reference multiple pages

  3. John E. McMurry - Wikipedia

    en.wikipedia.org/wiki/John_E._McMurry

    McMurry's most popular textbook Organic Chemistry was first printed in 1984. In 2022, he sold the rights for the book to OpenStax making it free for the user. [3] [4] Among his other texts are: Organic Chemistry with Biological Applications (3rd edition) [5] Chemistry (8th edition) [6] General Chemistry, Atoms First (2nd edition) [7]

  4. IUPAC Color Books - Wikipedia

    en.wikipedia.org/wiki/IUPAC_Color_Books

    It also includes a table of physical constants, tables listing the properties of elementary particles, chemical elements, and nuclides, and information about conversion factors that are commonly used in physical chemistry. The most recent edition is the third edition (ISBN 978-0-85404-433-7), originally published by IUPAC in 2007. A second ...

  5. Maitland Jones Jr. - Wikipedia

    en.wikipedia.org/wiki/Maitland_Jones_Jr.

    The head of NYU's Chemistry Department Mark Tuckerman, said that the decision not to renew Jones’s contract was made against the department’s recommendation, which was to have Jones teach organic chemistry to students majoring in chemistry, because chemistry majors would appreciate Jones' high standards. [7]

  6. Beilstein database - Wikipedia

    en.wikipedia.org/wiki/Beilstein_database

    The Beilstein database is a database in the field of organic chemistry, in which compounds are uniquely identified by their Beilstein Registry Number.The database covers the scientific literature from 1771 to the present and contains experimentally validated information on millions of chemical reactions and substances from original scientific publications.

  7. Friedrich Krafft - Wikipedia

    en.wikipedia.org/wiki/Friedrich_Krafft

    In organic chemistry, the Krafft degradation reaction is named after him. [2] This reaction is a conversion of a carboxylic acid , typically of high molecular weight, into the next lower homolog . He also established the boiling point of noble metals and synthesised aromatic compounds containing selenium and tellurium .