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  2. Diethylbenzenes - Wikipedia

    en.wikipedia.org/wiki/Diethylbenzenes

    C 6 H 6 + C 2 H 4 → C 6 H 5 C 2 H 5. The diethylbenzene is an inadvertent side product. C 6 H 5 C 2 H 5 + C 2 H 4 → C 6 H 4 (C 2 H 5) 2. Using shape-selective zeolite catalysts, the para isomer can be produced in high selectivity. Much diethylbenzene is recycled by transalkylation to give ethylbenzene: [1] C 6 H 4 (C 2 H 5) 2 + C 6 H 6 → ...

  3. C4-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C4-Benzenes

    The saturated compounds have formula C 10 H 14 and molecular weight 134.22 g/mol. C 4-benzenes are found in ... 1,3-Diethylbenzene. 1,4-Diethylbenzene. o-Cymene. m ...

  4. Divinylbenzene - Wikipedia

    en.wikipedia.org/wiki/Divinylbenzene

    It is produced by dehydrogenation of diethylbenzene: C 6 H 4 (C 2 H 5) 2 → C 6 H 4 (C 2 H 3) 2 + 2 H 2. Divinylbenzene is usually encountered as a 2:1 mixture of m- and p-divinylbenzene, containing also the corresponding isomers of ethylvinylbenzene. Styrene and divinylbenzene react to form the copolymer styrene-divinylbenzene, S-DVB or Sty-DVB.

  5. Color Developing Agent 1 - Wikipedia

    en.wikipedia.org/wiki/Color_Developing_Agent_1

    Color Developing Agent 1 (CD-1) is the first in the series of color developing agents used in developing color films. It is the organic compound N , N -diethyl-1,4-benzenediamine (DPD), which is usually in the form of the mono hydrochloride salt. [ 1 ]

  6. p-Xylene - Wikipedia

    en.wikipedia.org/wiki/P-Xylene

    The p-stands for para-, indicating that the two methyl groups in p-xylene occupy the diametrically opposite substituent positions 1 and 4. It is in the positions of the two methyl groups, their arene substitution pattern, that it differs from the other isomers, o-xylene and m-xylene. All have the same chemical formula C 6 H 4 (CH 3) 2. All ...

  7. Ethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Ethylbenzene

    Ethylbenzene is an organic compound with the formula C 6 H 5 CH 2 CH 3.It is a highly flammable, colorless liquid with an odor similar to that of gasoline.This monocyclic aromatic hydrocarbon is important in the petrochemical industry as a reaction intermediate in the production of styrene, the precursor to polystyrene, a common plastic material.

  8. Benzene (data page) - Wikipedia

    en.wikipedia.org/wiki/Benzene_(data_page)

    30.77 kJ/mol at 80.1 °C Std entropy change of vaporization, Δ vap S o: 113.6 J/(mol·K) at 25 °C 87.1 J/(mol·K) at 80.1 °C Solid properties Std enthalpy change of formation, Δ f H o solid? kJ/mol Standard molar entropy, S o solid: 45.56 J/(mol K) Heat capacity, c p: 118.4 J/(mol K) at 0 °C Liquid properties Std enthalpy change of ...

  9. m-Xylene - Wikipedia

    en.wikipedia.org/wiki/M-Xylene

    The m-stands for meta-, indicating that the two methyl groups in m-xylene occupy positions 1 and 3 on a benzene ring. It is in the positions of the two methyl groups, their arene substitution pattern, that it differs from the other isomers, o-xylene and p-xylene. All have the same chemical formula C 6 H 4 (CH 3) 2. All xylene isomers are ...