Abstract
Though the Fischer-Tropsch reaction is not a new topic in the world of science, the mechanism for the reaction is still unknown. After acquiring several different products from the Fischer-Tropsch reaction, it is possible to run analysis of these products against known branched carbon chains to identify the mechanism of the reaction. In order to synthesize these specific branched carbon chains, the Grignard, elimination, and hydrogenation reactions were used. This process takes reactants from a ketone to a branched alkane carbon chain. After trial and error in developing a procedure and adjusting the variables in each reaction, the series was able to consistently produce successful results and yields of the carbon chains. For the eight, ten, and eleven carbon chains we were able to synthesize 2 and 3 methyl branched compounds. The next step to correctly define the mechanism for the Fischer-Tropsch reaction is to run analysis of the products acquired from the Fischer-Tropsch reaction against the synthesized branched carbon chains.
Semester/Year of Award
Spring 5-5-2012
Mentor
Buchang Shi
Mentor Department Affiliation
Chemistry
Access Options
Restricted Access Thesis
Document Type
Bachelor Thesis
Degree Name
Honors Scholars
Degree Level
Bachelor's
Department
Chemistry
Recommended Citation
Montavon, Alexander H., "Synthesis of Branched Hydrocarbons Used for Identification of the Fischer-Tropsch Products" (2012). Honors Theses. 16.
https://encompass.eku.edu/honors_theses/16
