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tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.
The molecular formula C 4 H 9 Br, (molar mass: 137.02 g/mol, exact mass: 135.9888 u) may refer to: 1-Bromobutane; 2-Bromobutane; tert-Butyl bromide; 1-bromo-2 ...
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.
2-Bromo-2-methylpropane (tert-butyl bromide) Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.
Both compounds share the molecular formula C 4 H 9 Br. 2-Bromobutane is also known as sec-butyl bromide or methylethylbromomethane. Because it contains bromine, a halogen, it is part of a larger class of compounds known as alkyl halides. It is a colorless liquid with a pleasant odor.
Chemical formula Synonyms CAS number Ac 2 O 3: actinium(III) oxide: 12002-61-8 AgBF 4: Silver tetrafluoroborate: 14104-20-2 AgBr: silver bromide: 7785-23-1 AgBrO: silver hypobromite: AgBrO 2: silver bromite: AgBrO 3: silver bromate: 7783-89-3 AgBrO 4: silver perbromate: AgCl: silver chloride: 7783-90-6 AgCl 3 Cu 2: dicopper silver trichloride ...
The intermediate in this synthesis is di-tert-butylcyclopentadiene. This compound is conveniently prepared by alkylation of cyclobutadiene with tert-butyl bromide under phase-transfer conditions. [2] [1] Illustrative of the unusual complexes made possible with these bulky ligands is molecular iron nitrido complex (t Bu 3 C 5 H 2) 2 Fe 2 N 2. [3]
The tert-butoxide is a strong, non-nucleophilic base in organic chemistry. It readily abstracts acidic protons from substrates, but its steric bulk inhibits the group from participating in nucleophilic substitution, such as in a Williamson ether synthesis or an S N 2 reaction. tert-Butyl alcohol reacts with hydrogen chloride to form tert-butyl ...