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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 → ...
The C 4-benzenes are a class of organic aromatic compounds which contain a benzene ring and four other carbon atoms. There are three tetramethylbenzenes , six dimethylethylbenzenes, three diethylbenzenes , three isopropylmethylbenzenes , three n -propylmethylbenzenes and four butylbenzenes .
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 ...
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 ]
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.
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 ...
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They have been generated by decarboxylation of benzene dipropynoic acids, using the technique of mass spectrometry. [ 1 ] [ 2 ] The three isomers of the dianion are the three strongest known superbases ever, with the ortho isomer being the strongest, with a proton affinity of 1,843.987 kJ/mol (440.723 kcal/mol). [ 1 ]