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  2. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    Benzoic acid (/ b ɛ n ˈ z oʊ. ɪ k /) is a white (or colorless) solid organic compound with the formula C 6 H 5 COOH, whose structure consists of a benzene ring (C 6 H 6) with a carboxyl (−C(=O)OH) substituent.

  3. 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 − ...

  4. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol is not considered to be a carcinogen, and no data are available regarding teratogenic or reproductive effects. [5] Benzyl alcohol has low acute toxicity with an LD 50 of 1.2 g/kg in rats. [5] It oxidizes rapidly in healthy individuals to benzoic acid, conjugated with glycine in the liver, and excreted as hippuric acid. Very high ...

  5. Benzyl benzoate - Wikipedia

    en.wikipedia.org/wiki/Benzyl_benzoate

    The conjugates of benzoic acid (hippuric acid and the glucuronide of benzoic acid) are rapidly eliminated in urine. [1] When given in large doses to laboratory animals, benzyl benzoate can cause hyperexcitation, loss of coordination, ataxia, convulsions, and respiratory paralysis. [10] Benzyl benzoate can be a skin irritant when used as a ...

  6. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    Benzyl group and derivatives: Benzyl group, benzyl radical, benzyl amine, benzyl bromide, benzyl chloroformate, and benzyl methyl ether. R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5.

  7. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    In organic synthesis, benzyl chloride is used to introduce the benzyl protecting group in reaction with alcohols, yielding the corresponding benzyl ether, carboxylic acids, and benzyl ester. Benzoic acid (C 6 H 5 COOH) can be prepared by oxidation of benzyl chloride in the presence of alkaline KMnO 4: C 6 H 5 CH 2 Cl + 2 KOH + 2 [O] → C 6 H 5 ...

  8. Benzhydryl compounds - Wikipedia

    en.wikipedia.org/wiki/Benzhydryl_compounds

    Ball-and-stick model of diphenylmethane. The benzhydryl compounds are a group of organic compounds whose parent structures include diphenylmethane (which is two benzene rings connected by a single methane), with any number of attached substituents, including bridges.

  9. Benzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde

    Amygdalin 2 H 2 O HCN benzaldehyde 2 × glucose 2 × Benzaldehyde contributes to the scent of oyster mushrooms (Pleurotus ostreatus). Reactions Benzaldehyde is easily oxidized to benzoic acid in air at room temperature, causing a common impurity in laboratory samples. Since the boiling point of benzoic acid is much higher than that of benzaldehyde, it may be purified by distillation. Benzyl ...