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Tert-butyl bromide

Write a series of equations describing a synthesis of 1 bromo 2 Tietny rop ol from tert butyl bromide J... [Pg.266]

Hughes and Ingold observed that the hydrolysis of tert butyl bromide which occurs readily is characterized by a first order rate law... [Pg.339]

They found that the rate of hydrolysis depends only on the concentration of tert butyl bromide Adding the stronger nucleophile hydroxide ion moreover causes no change m... [Pg.339]

Suggest a structure for the product of nucleophilic substitution obtained on solvolysis of tert-butyl bromide in methanol and outline a reason able mechanism for its formation... [Pg.340]

FIGURE 8 5 The SnI mecha nism for hydrolysis of tert butyl bromide... [Pg.340]

The real world of Sn reactions is not quite as simple as the discussion has so far suggested. The preceding treatment in terms of two clearly distinct mechanisms, SnI and Sn2, implies that all substitution reactions will follow one or the other of these mechanisms. This is an oversimplification. The strength of the dual mechanism hypothesis and its limitations are revealed by these relative rates of solvolysis of alkyl bromides in 80% ethanol methyl bromide, 2.51 ethyl bromide, 1.00 isopropyl bromide, 1.70 /er/-butyl bromide, 8600. Addition of lyate ions increases the rate for the methyl, ethyl, and isopropyl bromides, whereas the tert-butyl bromide solvolysis rate is unchanged. The reaction with lyate ions is overall second-order for methyl and ethyl, first-order for tert-butyl, and first- or second-order for the isopropyl member, depending upon the concentrations. Similar results are found in other solvents. These data show that the methyl and ethyl bromides solvolyze by the Sn2 mechanism, and tert-butyl bromide by the SnI mech-... [Pg.428]

Xu, M. Basile, F. Voorhees, K. J. Differentiation and classification of user-specified bacterial groups by in situ thermal hydrolysis and methylation of whole bacterial cells with tert-butyl bromide chemical ionization ion trap mass spectrometry. Anal. Chim. Acta 2000, 418,119-128. [Pg.298]

Cool flame behaviour of acetaldehyde is apparently eliminated by tert-butyl bromide, and reduced by methyl iodide. [Pg.312]

Bromo-2-methylpropane l-Chloro-2-methylpropane tert-Butyl bromide Isobutyl chloride... [Pg.135]

Methylpropene tert-Butyl bromide Isobutyl bromide... [Pg.322]

The reaction of HBr with 2-methylpropene produces only tert-butyl bromide. [Pg.326]

Butyl bromide, b274 sec-Butyl bromide, b275 tert-Butyl bromide, b372 iV-Butyl-l -butanamine, dl39 Butyl butenoate, b531... [Pg.131]

Kinetic data at 25 C for the conversion of tert-butyl bromide to tert-butyl alcohol in a solvent of 90% acetone and 10% water are tabulated. Time is in hours, concentration in gmol/liter. Find the rate equation. [Pg.153]

Figure 10 The dependence of conductivity on concentration for a mixture of aluminium bromide and tert-butyl bromide (mole ratio 1 1) in methyl bromide... Figure 10 The dependence of conductivity on concentration for a mixture of aluminium bromide and tert-butyl bromide (mole ratio 1 1) in methyl bromide...

See other pages where Tert-butyl bromide is mentioned: [Pg.334]    [Pg.334]    [Pg.335]    [Pg.340]    [Pg.340]    [Pg.341]    [Pg.359]    [Pg.359]    [Pg.372]    [Pg.386]    [Pg.141]    [Pg.334]    [Pg.341]    [Pg.358]    [Pg.359]    [Pg.359]    [Pg.386]    [Pg.433]    [Pg.905]    [Pg.1319]    [Pg.1324]    [Pg.1396]    [Pg.2318]    [Pg.326]    [Pg.94]    [Pg.111]    [Pg.1029]    [Pg.153]    [Pg.315]   
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See also in sourсe #XX -- [ Pg.179 , Pg.238 ]

See also in sourсe #XX -- [ Pg.150 , Pg.204 ]

See also in sourсe #XX -- [ Pg.144 ]




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4-tert-Butyl cyclohexyl bromide

4-tert-Butyl cyclohexyl bromide trans isomers

Bromide,tert

Butyl acetate bromide,tert

Butyl bromide

Butylated butyl bromide

Hydrolysis of tert butyl bromide

Magnesium tert-butyl bromide

Tert Butyl bromide nucleophilic substitution

Tert-Butyl bromide 2-methylpropene

Tert-Butyl bromide benzene

Tert-Butyl bromide intermediate

Tert-Butyl bromide polymerization

Tert-Butyl bromide stability

Tert-Butyl bromide with hydrogen chloride

Tert-Butyl bromide, derivative

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