Elimination Reactions over Polar Catalysts: Mechanistic Considerations
- 1 January 1976
- journal article
- research article
- Published by Taylor & Francis in Catalysis Reviews
- Vol. 13 (1) , 149-207
- https://doi.org/10.1080/00087647608069937
Abstract
In order to form a double bond in an organic molecule, two fragments (atoms or groups) are abstracted from adjacent carbon atoms. Such a reaction is called a β-elimination [12, 221. In many cases one of the fragments is hydrogen.Keywords
This publication has 95 references indexed in Scilit:
- X, Y, aluminum-deficient, and ultrastable faujasite-type zeolites III. Catalytic activityJournal of Catalysis, 1973
- The role of the proton in the catalytic cracking of hexane using a zeolite catalystJournal of Catalysis, 1971
- On the mechanisms of contact eliminations *1XXIX. The elimination of CH3COOH from gaseous ethyl, n-propyl and n-butyl acetate over salt catalysts: The influence of the reactant structure on the reaction rateJournal of Catalysis, 1971
- Zum Mechanismus von KontakteliminierungenZeitschrift für Physikalische Chemie, 1968
- Alumina: catalyst and support. XXXVII. Mechanism of dehydration of cis- and trans-2-alkyl-, 2-phenyl- and 3-tert-butylcyclohexanols over alumina catalystsThe Journal of Organic Chemistry, 1968
- Dehydratisierung von gasförmigem [2‐D]‐2‐Butanol an CaSO4Angewandte Chemie, 1968
- Relationship between catalytic activity and nature of acidity of the crystalline zeolites, mordenite and Y faujasiteJournal of Catalysis, 1967
- Dehydration of alcohols over zeolite catalystsJournal of Catalysis, 1967
- Infrared Spectroscopic Investigations of Zeolites and Adsorbed Molecules. I. Structural OH Groups1The Journal of Physical Chemistry, 1965
- Crystalline molecular sievesJournal of Chemical Education, 1964