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  2. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    These aromatic compounds are classed as phenols. There are three structural isomers: 1,2-dihydroxybenzene (the ortho isomer) is commonly known as catechol, 1,3-dihydroxybenzene (the meta isomer) is commonly known as resorcinol, and 1,4-dihydroxybenzene (the para isomer) is commonly known as hydroquinone. [1]

  3. Ortho effect - Wikipedia

    en.wikipedia.org/wiki/Ortho_effect

    When protonated, the nitrogen in the amino group changes its orbital hybridization from sp 2 to sp 3, becoming non-planar. This leads to steric hindrance between the ortho-substituted group and the hydrogen atom of the amino group, reducing the stability of the conjugate acid and consequently decreasing the pH of substituted aniline.

  4. Catechol - Wikipedia

    en.wikipedia.org/wiki/Catechol

    Catechol (/ ˈ k æ t ɪ tʃ ɒ l / or / ˈ k æ t ɪ k ɒ l /), also known as pyrocatechol or 1,2-dihydroxybenzene, is an organic compound with the molecular formula C 6 H 4 (OH) 2. It is the ortho isomer of the three isomeric benzenediols .

  5. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    CH 3 CH 2 OH . Parentheses are used to indicate multiple identical groups, indicating attachment to the nearest non-hydrogen atom on the left when appearing within a formula, or to the atom on the right when appearing at the start of a formula: (CH 3) 2 CHOH or CH(CH 3) 2 OH . In all cases, all atoms are shown, including hydrogen atoms.

  6. Haloform reaction - Wikipedia

    en.wikipedia.org/wiki/Haloform_reaction

    In chemistry, the haloform reaction (also referred to as the Lieben haloform reaction) is a chemical reaction in which a haloform (CHX 3, where X is a halogen) is produced by the exhaustive halogenation of an acetyl group (R−C(=O)CH 3, where R can be either a hydrogen atom, an alkyl or an aryl group), in the presence of a base.

  7. Phenylsilane - Wikipedia

    en.wikipedia.org/wiki/Phenylsilane

    Phenylsilane, also known as silylbenzene, a colorless liquid, is one of the simplest organosilanes with the formula C 6 H 5 SiH 3. It is structurally related to toluene, with a silyl group replacing the methyl group. Both of these compounds have similar densities and boiling points due to these similarities. Phenylsilane is soluble in organic ...

  8. Trihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Trihydroxybenzenes

    The trihydroxybenzenes (or benzenetriols) are organic compounds with the formula C 6 H 3 (OH) 3. Also classified as polyphenols, they feature three hydroxyl groups substituted onto a benzene ring. They are white solids with modest solubility in water.

  9. Mesitylene - Wikipedia

    en.wikipedia.org/wiki/Mesitylene

    Mesitylene or 1,3,5-trimethylbenzene is a derivative of benzene with three methyl substituents positioned symmetrically around the ring. The other two isomeric trimethylbenzenes are 1,2,4-trimethylbenzene (pseudocumene) and 1,2,3-trimethylbenzene (hemimellitene). All three compounds have the formula C 6 H 3 (CH 3) 3, which is commonly ...