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  2. 1,2-Dinitrobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2-Dinitrobenzene

    1,2-Dinitrobenzene is one of three isomers of dinitrobenzene, with the formula C 6 H 4 (NO 2) 2. The compound is a white or colorless solid that is soluble in organic solvents. It is prepared from 2-nitroaniline by diazotization and treatment with sodium nitrite in the presence of a copper catalyst. [1]

  3. Dinitrobenzene - Wikipedia

    en.wikipedia.org/wiki/Dinitrobenzene

    The three possible arrangements of the nitro groups afford three isomers, 1,2-dinitrobenzene, 1,3-dinitrobenzene, and 1,4-dinitrobenzene. Each isomer has the chemical formula C 6 H 4 N 2 O 4 and a molar mass of about 168.11 g/mol. 1,3-Dinitrobenzene is the most common isomer and it is used in the manufacture of explosives.

  4. Ortho effect - Wikipedia

    en.wikipedia.org/wiki/Ortho_effect

    In contrast, 2-methyl-1,4-dinitrobenzene (2c) is isolated in only 9.9% yield. [4] As witnessed in the above example, when a π-acceptor substituent (πAS) is meta to a π-donor substituent (πDS), the electrophilic aromatic nitration occurs ortho to the πAS rather than para.

  5. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  6. Hansen solubility parameter - Wikipedia

    en.wikipedia.org/wiki/Hansen_solubility_parameter

    Hansen solubility parameters were developed by Charles M. Hansen in his Ph.D thesis in 1967 [1] [2] as a way of predicting if one material will dissolve in another and form a solution. [3] They are based on the idea that like dissolves like where one molecule is defined as being 'like' another if it bonds to itself in a similar way.

  7. m-Phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/M-Phenylenediamine

    m-Phenylenediamine, also called 1,3-diaminobenzene, is an organic compound with the formula C 6 H 4 (NH 2) 2.It is an isomer of o-phenylenediamine and p-phenylenediamine.This aromatic diamine is a colourless solid that appears as needles, but turns red or purple on exposure to air due to formation of oxidation products. [3]

  8. Why Diversity Matters Catalyst 7-16-12 - HuffPost

    images.huffingtonpost.com/2013-03-21-why...

    average, about 10 percent more profitable than corresponding companies with men CEOs.19 USA Today compared the stocks of 13 Fortune 500 companies with women CEOs to the stocks of the overall S&P 500 and found that in 2009 the women-led companies were up an average of 50 percent, while the S&P 500 was up 25 percent.20

  9. Nitrobenzenes - Wikipedia

    en.wikipedia.org/wiki/Nitrobenzenes

    Nitrobenzenes are a group of nitro compounds consisting of one or more nitro groups as substituents on a benzene core. They have the formula C 6 H 6–n (NO 2) n, where n = 1–6 is the number of nitro groups. Depending on the number of nitro groups, there may be several constitutional isomers possible. Mononitrobenzene; Dinitrobenzene. 1,2 ...