bromination

The reaction mechanism for an alkene bromination can be described as follows.

An example is the bromination of acetone in basic solution:

Most commonly bromination is conducted by the addition of Br to alkenes.

Like other esters, this compound undergoes bromination at the alpha position.

"But even the best bromination won't be effective in a situation where the bacteria hide in sediment," he said.

The compound is prepared by bromination of acetic acid.

A lot of reactions derive their name from the reagent involved like bromination or acylation.

Tribromoisocyanuric acid is used for the bromination of aromatics and alkenes.

An example of radical bromination of toluene is given below:

Bisphenol A compounds with lower degrees of bromination seem to exhibit greater estrogenicity.

Bromination and iodination work best, though this reaction does not preserve the stereochemistry of the alcohol.

The classical example of this is bromination (any halogenation) of alkenes.

Alternatively, it can be prepared by the bromination of tetraline (1,2,3,4-tetrahydronaphthalene):

Chlorination is generally less selective than bromination.

Bromination is more selective than chlorination because the reaction is less exothermic.

Mucobromic acid can be synthesized by bromination of furfural.

Bromatometry is a titration process in which the bromination of a chemical indicator is observed.

The first step in this reaction involves the bromination followed by cyclization of cyclooctatriene to form a cyclohexadiene.

Bromoperoxidases are enzymes that catalyse the bromination of hydrocarbons.

Her dissertation was "The bromination of naphthalene."

The most prominent member is tetrabromobisphenol-A, which is prepared by direct bromination of the diphenol.

The mixture resulting from the bromination of bisphenol A is therefore not purified, allowing a more efficient, lower cost product.

It is prepared by methane bromination using HBr or Br.

It undergoes bromination to give dibromoacrylic acid.