Search results
Results from the WOW.Com Content Network
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.
This page was last edited on 27 December 2022, at 15:12 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).
n-Butylbenzene is the organic compound with the formula C 6 H 5 C 4 H 9.Of two isomers of butylbenzene, n-butylbenzene consists of a phenyl group attached to the 1 position of a butyl group.
Butyl ester may refer to: Butyl nitrite; The family of organic chemical compounds containing an ester group and a butyl group including: Butyl acetate; Butyl acrylate;
Butyl group From a page move : This is a redirect from a page that has been moved (renamed). This page was kept as a redirect to avoid breaking links, both internal and external, that may have been made to the old page name.
Pentanenitrile, valeronitrile or butyl cyanide is a nitrile with the formula C 4 H 9 CN. This can be written BuCN, with Bu representing an n -butyl (linear butyl group ). Production
About the reaction scheme under the heading "tert-butyl effect", I believe the product is incorrect, as there is an extra carbon atom present. The reaction as stated would form a 6- and 4-membered ring, not a 6- and 5-membered ring as shown.