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  2. Benzoyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_peroxide

    Benzoyl peroxide is a chemical compound (specifically, an organic peroxide) with structural formula (C 6 H 5 −C(=O)O−) 2, often abbreviated as (BzO) 2.In terms of its structure, the molecule can be described as two benzoyl (C 6 H 5 −C(=O)−, Bz) groups connected by a peroxide (−O−O−).

  3. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Dialkyl peroxides, e.g., dicumyl peroxide, are synthesized by addition of hydrogen peroxide to alkenes or by O-alkylation of hydroperoxides. Diacyl peroxides are typically prepared by treating hydrogen peroxide with acid chlorides or acid anhydrides in the presence of base: [1] H 2 O 2 + 2 RCOCl → (RCO 2) 2 + 2 HCl H 2 O 2 + (RCO) 2 O → ...

  4. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    In organic chemistry, benzoyl (/ ˈ b ɛ n z oʊ ɪ l /, BENZ-oh-il) [1] is the functional group with the formula −COC 6 H 5 and structure −C(=O)−C 6 H 5. [2] [3] It can be viewed as benzaldehyde missing one hydrogen. The benzoyl group has a mass of 105 amu. The term "benzoyl" should not be confused with benzyl, which has the formula − ...

  5. Peroxide - Wikipedia

    en.wikipedia.org/wiki/Peroxide

    In addition to hydrogen peroxide, some other major classes of peroxides are: Peroxy acids, the peroxy derivatives of many familiar acids, examples being peroxymonosulfuric acid and peracetic acid, and their salts, one example of which is potassium peroxydisulfate. Main group peroxides, compounds with the linkage E−O−O−E (E = main group ...

  6. Homolysis (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Homolysis_(chemistry)

    The O-O σ bond in dibenzoyl peroxide is cleaved homolytically, distributing a radical to each benzoyloxy. Heat Certain intramolecular bonds, such as the O–O bond of a peroxide, are sufficiently weak to spontaneously homolytically dissociate near room temperature. Most bonds homolyse at temperatures above 200°C. [4]

  7. The best benzoyl peroxide products, according to ... - AOL

    www.aol.com/news/best-benzoyl-peroxide-products...

    This includes hyaluronic acid, glycerin, ceramides and niacinamide, according to our experts. Concentration: The strength of your over-the-counter benzoyl peroxide will range from 2.5% to 10%. The ...

  8. Peroxybenzoic acid - Wikipedia

    en.wikipedia.org/wiki/Peroxybenzoic_acid

    Peroxybenzoic acid is an organic compound with the formula C 6 H 5 CO 3 H. It is the simplest aryl peroxy acid . It may be synthesized from benzoic acid and hydrogen peroxide , [ 3 ] or by the treatment of benzoyl peroxide with sodium methoxide , followed by acidification.

  9. Main group peroxides - Wikipedia

    en.wikipedia.org/wiki/Main_group_peroxides

    The structure of the peroxodisulfate anion. In chemistry, main group peroxides are peroxide derivatives of the main group elements. Many compounds of the main group elements form peroxides (R−O−O−R'), and a few are of commercial significance. [1]