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  2. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    The efficacy of benzoic acid and benzoate is thus dependent on the pH of the food. [24] Benzoic acid, benzoates and their derivatives are used as preservatives for acidic foods and beverages such as citrus fruit juices ( citric acid ), sparkling drinks ( carbon dioxide ), soft drinks ( phosphoric acid ), pickles ( vinegar ) and other acidified ...

  3. Ortho effect - Wikipedia

    en.wikipedia.org/wiki/Ortho_effect

    Ortho effect is an organic chemistry phenomenon where the presence of a chemical group at the at ortho position or the 1 and 2 position of a phenyl ring, relative to the carboxylic compound changes the chemical properties of the compound.

  4. 4-Bromobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-bromobenzaldehyde

    4-Bromobenzaldehyde, or p-bromobenzaldehyde, is an organobromine compound with the formula BrC 6 H 4 CHO. It is one of three isomers of bromobenzaldehyde . [ 3 ] It displays reactivity characteristic of benzaldehyde and an aryl bromide .

  5. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    Many ketones contain the benzoyl group. They have the formula C 6 H 5 CO–R, an important example being benzophenone. Benzoyl esters and amides are common in organic chemistry. The esters are used as a protecting groups in organic synthesis, [4] which can be easily removed by hydrolysis in dilute basic solution.

  6. Von Richter reaction - Wikipedia

    en.wikipedia.org/wiki/Von_Richter_reaction

    The reaction is a type of nucleophilic aromatic substitution. [4] Besides the bromo derivative, chlorine- and iodine-substituted nitroarenes, as well as more highly substituted derivatives, could also be used as substrates of this reaction. However, yields are generally poor to moderate, with reported percentage yields ranging from 1% to 50% ...

  7. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    This reagent can be used, e.g. in the reaction with carbon dioxide to prepare benzoic acid. [4] Other methods involve palladium-catalyzed coupling reactions , such as the Suzuki reaction . Bromobenzene is used as a precursor in the manufacture of phencyclidine .

  8. Benzene in soft drinks - Wikipedia

    en.wikipedia.org/wiki/Benzene_in_soft_drinks

    The major cause of benzene in soft drinks is the decarboxylation of benzoic acid in the presence of ascorbic acid (vitamin C, E300) or erythorbic acid (a diastereomer of ascorbic acid, E315). Benzoic acid is often added to drinks as a preservative in the form of its salts sodium benzoate (E211), potassium benzoate (E 212), or calcium benzoate ...

  9. 4-Hydroxybenzoic acid - Wikipedia

    en.wikipedia.org/wiki/4-Hydroxybenzoic_acid

    4-Hydroxybenzoic acid, also known as p-hydroxybenzoic acid (PHBA), is a monohydroxybenzoic acid, a phenolic derivative of benzoic acid.It is a white crystalline solid that is slightly soluble in water and chloroform but more soluble in polar organic solvents such as alcohols and acetone. 4-Hydroxybenzoic acid is primarily known as the basis for the preparation of its esters, known as parabens ...