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The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.
Firstly, 2,4-dimethyl-6-tert-butylphenol is reacted with formaldehyde and HCl (Blanc reaction) to generate a chloromethyl group in the less hindered meta position. This intermediate then reacts with cyanuric acid to give the desired product.
The effect of the tert-butyl group on the progress of a chemical reaction is called the Thorpe–Ingold effect illustrated in the Diels-Alder reaction below. Compared to a hydrogen substituent, the tert-butyl substituent accelerates the reaction rate by a factor of 240. [2] tert-Butyl effect. The tert-butyl effect is an example of steric hindrance.
3,3-Di-tert-butyl-2,2,4,4-tetramethylpentane; Heptadecane This page was last edited on 2 May 2021, at 18:22 (UTC). Text is available under the Creative Commons ...
It can be prepared by base-catalyzed isomerization of 2,3-dimethyl-1-butene. [2] Another route involves direct dimerization of propylene . [ 3 ] It can also be produced by photolysis of tetramethylcyclobutane-1,3-dione .
9.11 tert-Butyl+Ethyl+Dimethyl. 10 With pentane backbone. 11 References. Toggle the table of contents. List of isomers of tetradecane. ... 2,3,4,5,6,7-Hexamethyloctane;