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7.7 tert-Butyl+Dimethyl. 8 Pentane. Toggle Pentane subsection. 8.1 Ethyl+Pentamethyl. ... 3,5-Dimethyl-4-(1-methylethyl)heptane; Ethyl+Propyl. 3-Ethyl-4-propylheptane;
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.
tert-Butyl alcohol is the simplest tertiary alcohol, with a formula of (CH 3) 3 COH (sometimes represented as t-BuOH). Its isomers are 1-butanol, isobutanol, and butan-2-ol. tert-Butyl alcohol is a colorless solid, which melts near room temperature and has a camphor-like odor. It is miscible with water, ethanol and diethyl ether.
The density and boiling are the lowest of the isomers of heptane. The dielectric constant is 1.915, the lowest of the heptane isomers. The critical temperature is 247.7 °C and critical pressure 28.4 atmospheres. The refractive index at 20° is 1.38233, the same as for 2,4-dimethylpentane, equal lowest for the heptane isomers.
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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 .