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  2. Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/Nitrobenzoic_acid

    2-Nitrobenzoic acid is prepared by oxidation of 2-nitrotoluene. 3-Nitrobenzoic acid is a precursor to 3-aminobenzoic acid, which in turn is used to prepare some dyes. It can be prepared by nitration of benzoic acid. It also can be prepared by treating benzaldehyde under nitration conditions, a process that initially converts the aldehyde to the ...

  3. 3-Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/3-Nitrobenzoic_acid

    3-Nitrobenzoic acid is an organic compound with the formula C 6 H 4 (NO 2)CO 2 H. It is an aromatic compound and under standard conditions, it is an off-white solid. The two substituents are in a meta position with respect to each other, giving the alternative name of m-nitrobenzoic acid.

  4. 4-Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/4-Nitrobenzoic_acid

    4-Nitrobenzoic acid is prepared by oxidation of 4-nitrotoluene using oxygen or dichromate as oxidants. [7] Alternatively, it has been prepared by nitration of polystyrene followed by oxidation of the alkyl substituent. This method proceeds with improved para/ortho selectivity owing to the steric protection of the ortho positions by the polymer ...

  5. Nitration - Wikipedia

    en.wikipedia.org/wiki/Nitration

    In addition to regioselectivity, the degree of nitration is of interest. Fluorenone, for example, can be selectively trinitrated [10] or tetranitrated. [11] The direct nitration of aniline with nitric acid and sulfuric acid, according to one source, [12] results in a 50/50 mixture of para- and meta-nitroaniline isomers.

  6. 2-Nitrobenzoic acid - Wikipedia

    en.wikipedia.org/wiki/2-Nitrobenzoic_acid

    2-Nitrobenzoic acid or o-nitrobenzoic acid is an organic compound with the formula C 6 H 4 (NO 2)CO 2 H. It is prepared by oxidation of 2-nitrotoluene with nitric acid. [1] In consists of a carboxylic acid group and a nitro group in the ortho configuration. Reduction of the nitro group into an amine produces anthranilic acid.

  7. Ortho effect - Wikipedia

    en.wikipedia.org/wiki/Ortho_effect

    Nitration of 3-Methylbenzoic acid. Similar results were also observed on the nitration of 3-methylbenzoic acid in which 5-methyl-2-nitrobenzoic acid and 3-methyl-2-nitrobenzoic acid were obtained as the major compounds, whereas 3-methyl-4-nitrobenzoic acid was reported as a minor compound. [5]

  8. 9 Foods That Smell Awful but Taste Amazing - AOL

    www.aol.com/9-foods-smell-awful-taste-170000841.html

    Kimchi's strong smell comes from sulfur compounds released during fermentation, produced by lactic acid bacteria breaking down vegetable sugars. brebca/istockphoto. 5. Truffle Oil.

  9. Nitrobenzene - Wikipedia

    en.wikipedia.org/wiki/Nitrobenzene

    Nitrobenzene is prepared by nitration of benzene with a mixture of concentrated sulfuric acid, water, and nitric acid. This mixture is sometimes called "mixed acid." The production of nitrobenzene is one of the most dangerous processes conducted in the chemical industry because of the exothermicity of the reaction (ΔH = −117 kJ/mol). [5] +