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  2. Ortho effect - Wikipedia

    en.wikipedia.org/wiki/Ortho_effect

    Also in nitration of the nitration of 3-bromobenzoic acid 5-bromo-2-nitrobenzoic acid (83%yield) was obtained as major product and 3-bromo-2-nitrobenzoic acid (13% yield) as minor. On an interesting note the potential isomer 3-bromo-4-nitrobenzoic acid was not detected.

  3. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    [3] Bromobenzene is used to introduce a phenyl group into other compounds. One method involves its conversion to the Grignard reagent, phenylmagnesium bromide. This reagent can be used, e.g. in the reaction with carbon dioxide to prepare benzoic acid. [4] Other methods involve palladium-catalyzed coupling reactions, such as the Suzuki reaction.

  4. Anisic acid - Wikipedia

    en.wikipedia.org/wiki/Anisic_acid

    Anisic acid or methoxybenzoic acid is an organic compound which is a carboxylic acid. It exists in three forms, depending on arene substitution patterns: p-Anisic acid (4-methoxybenzoic acid) m-Anisic acid (3-methoxybenzoic acid) o-Anisic acid (2-methoxybenzoic acid)

  5. 3-Fluorobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3-Fluorobenzoic_acid

    3-Fluorobenzoic acid is an organic compound with the formula C 7 H 5 FO 2. It is the meta form of fluorobenzoic acid. Its conjugate base is 3-fluorobenzoate. The compound is an irritant. Its acidity (pKa) is lower than that of the ortho form (2-fluorobenzoic acid) but higher than that of the para form (4-fluorobenzoic acid). It has been used in ...

  6. Bromochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromochlorobenzene

    All three have been synthesized by various routes: 1-Bromo-2-chlorobenzene: from 2-chloroaniline, via diazotization followed by a Sandmeyer reaction [1]; 1-Bromo-3-chlorobenzene: by (3-chlorophenyl)trimethylgermanium by electrophilic substitution [2] [better source needed]

  7. Bromophenol - Wikipedia

    en.wikipedia.org/wiki/Bromophenol

    Chemical structure of 2-bromophenol. A bromophenol is an organic compound consisting of hydroxyl groups and bromine atoms bonded to a benzene ring. They may be viewed as hydroxyl derivatives of bromobenzene, or as brominated derivatives of phenol.

  8. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    Monobromotoluene isomers [1] [2] [3] Common name Structure Systematic name: 1-bromo-2-methylbenzene 1-bromo-3-methylbenzene 1-bromo-4-methylbenzene Molecular formula: C 7 H 7 Br (C 6 H 4 BrCH 3) Molar mass: 171.03 g/mol Appearance colorless liquid colorless liquid white crystalline solid CAS number [95-46-5] [591-17-3]

  9. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.