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  2. Benzoin condensation - Wikipedia

    en.wikipedia.org/wiki/Benzoin_condensation

    In the classic example, benzaldehyde is converted to benzoin (PhCH(OH)C(O)Ph). [3] The benzoin condensation was first reported in 1832 by Justus von Liebig and Friedrich Wöhler during their research on bitter almond oil. [4] The catalytic version of the reaction involving cyanide was developed by Nikolay Zinin in the late 1830s. [5] [6 ...

  3. Charge transfer coefficient - Wikipedia

    en.wikipedia.org/wiki/Charge_transfer_coefficient

    Charge transfer coefficient, and symmetry factor (symbols α and β, respectively) are two related parameters used in description of the kinetics of electrochemical reactions. They appear in the Butler–Volmer equation and related expressions. The symmetry factor and the charge transfer coefficient are dimensionless. [1]

  4. Hammett equation - Wikipedia

    en.wikipedia.org/wiki/Hammett_equation

    0<ρ<1, the reaction is less sensitive to substituents than benzoic acid and negative charge is built (or positive charge is lost). ρ=0, no sensitivity to substituents, and no charge is built or lost. ρ<0, the reaction builds positive charge (or loses negative charge). These relations can be exploited to elucidate the mechanism of a reaction.

  5. Benzoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_chloride

    Benzoyl chloride, also known as benzenecarbonyl chloride, is an organochlorine compound with the formula C 7 H 5 ClO. It is a colourless, fuming liquid with an irritating odour, and consists of a benzene ring ( C 6 H 6 ) with an acyl chloride ( −C(=O)Cl ) substituent .

  6. 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 − ...

  7. 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 ...

  8. Photochlorination - Wikipedia

    en.wikipedia.org/wiki/Photochlorination

    Benzyl chloride can also be converted via benzyl cyanide with subsequent hydrolysis into phenylacetic acid. [22] [23] The disubstituted benzal chloride is converted to benzaldehyde, a popular flavorant [24] and intermediate for the production of malachite green and other dyes. [25] The trisubstituted benzotrichloride is used for the hydrolysis ...

  9. Inner sphere electron transfer - Wikipedia

    en.wikipedia.org/wiki/Inner_sphere_electron_transfer

    Inner sphere electron transfer (IS ET) or bonded electron transfer [1] is a redox chemical reaction that proceeds via a covalent linkage—a strong electronic interaction—between the oxidant and the reductant reactants. In inner sphere electron transfer, a ligand bridges the two metal redox centers during the electron transfer event. Inner ...

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