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  2. Benzamide - Wikipedia

    en.wikipedia.org/wiki/Benzamide

    Benzamide is an organic compound with the chemical formula of C 7 H 7 NO. It is the simplest amide derivative of benzoic acid . In powdered form, it appears as a white solid, while in crystalline form, it appears as colourless crystals. [ 5 ]

  3. C7H7NO - Wikipedia

    en.wikipedia.org/wiki/C7H7NO

    The molecular formula C 7 H 7 NO (molar mass: 121.14 g/mol, exact mass: 121.0528 u) may refer to: 2-Acetylpyridine; 2-Aminobenzaldehyde; Benzamide; Formanilide

  4. Molar mass - Wikipedia

    en.wikipedia.org/wiki/Molar_mass

    Molar mass is closely related to the relative molar mass (M r) of a compound and to the standard atomic weights of its constituent elements. However, it should be distinguished from the molecular mass (which is confusingly also sometimes known as molecular weight), which is the mass of one molecule (of any single isotopic composition), and to ...

  5. Benzonitrile - Wikipedia

    en.wikipedia.org/wiki/Benzonitrile

    Benzonitrile is a useful solvent and a versatile precursor to many derivatives. It reacts with amines to afford N-substituted benzamides after hydrolysis. [3] It is a precursor to diphenylmethanimine via reaction with phenylmagnesium bromide followed by methanolysis.

  6. Ammonium benzoate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_benzoate

    Molar mass: 139.15 g/mol Appearance White solid Density: 1.26 g/cm 3: Melting point: ... Ammonium benzoate can be dehydrated to form benzamide. References

  7. Benzoic acid - Wikipedia

    en.wikipedia.org/wiki/Benzoic_acid

    The process uses abundant materials, and proceeds in high yield. [13] toluene oxidation. The first industrial process involved the reaction of benzotrichloride (trichloromethyl benzene) with calcium hydroxide in water, using iron or iron salts as catalyst. The resulting calcium benzoate is converted to benzoic acid with hydrochloric acid.

  8. Benzophenone - Wikipedia

    en.wikipedia.org/wiki/Benzophenone

    In this prototypical example involving benzophenone, the tetrahedral intermediate expels phenyl anion to give benzamide and benzene as the organic products. Benzophenone is a common photosensitizer in photochemistry. It crosses from the S 1 state into the triplet state with nearly 100% yield.

  9. Benzimidazole - Wikipedia

    en.wikipedia.org/wiki/Benzimidazole

    Benzimidazole is a base: . C 6 H 4 N(NH)CH + H + → [C 6 H 4 (NH) 2 CH] +. It can also be deprotonated with stronger bases: . C 6 H 4 N(NH)CH + LiH → Li [C 6 H 4 N 2 CH] + H 2. The imine can be alkylated and also serves as a ligand in coordination chemistry.

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