1,2-Diethylbenzene
| PubChem CID | 8657 |
|---|---|
| Structure | Find Similar Structures |
| Chemical Safety | Laboratory Chemical Safety Summary (LCSS) Datasheet |
| Molecular Formula | CH3CH2(C6H4)CH2CH3 or C10H14 |
| Synonyms | 1,2-DIETHYLBENZENE 135-01-3 o-Diethylbenzene Benzene, 1,2-diethyl- Benzene, diethyl- More… |
What is the molecular formula of 1/3-diethylbenzene?
C10H14
1,3-Diethylbenzene | C10H14 – PubChem.
What is the molar mass of C10H14?
134.22 g/molDurene / Molar mass
What is the density of 1/4 diethylbenzene?
0.860 – 0.865
1,4-Diethylbenzene for synthesis. CAS 105-05-5, molar mass 134.22 g/mol….Pricing & Availability.
| Specifications | |
|---|---|
| Density (d 20 °C/ 4 °C) | 0.860 – 0.865 |
| Identity (IR) | passes test |
What is boiling point of benzene?
176.2°F (80.1°C)Benzene / Boiling point
What is the boiling point of ethylbenzene?
276.8°F (136°C)Ethylbenzene / Boiling point
What is structure of anthracene?
C14H10Anthracene / Formula
Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C14H10, consisting of three fused benzene rings. It is a component of coal tar. Anthracene is used in the production of the red dye alizarin and other dyes.
What is aromaticity of anthracene?
Anthracene is solid in state and consists of polycyclic aromatic hydrocarbon. It has three fused benzene rings derived from coal tar. Complete step by step answer: For a compound considered aromatic, it follows Huckel’s rule and overlapping p orbitals in order to be aromatic.
What is the difference between P -diethylbenzene and p -Para?
Para: known as 1,4-diethylbenzene and p -diethylbenzene. Diethylbenzenes arise as side-products of the alkylation of benzene with ethylene, which can described as two steps. The first step is the industrial route to ethylbenzene, which is produced on a large scale as a precursor to styrene . The diethylbenzene is an inadvertent side product.
What is the formula for didiethylbenzene?
Diethylbenzene (DEB) refers to any of three isomers with the formula C 6 H 4 (C 2 H 5) 2. Each consists of a benzene ring and two ethyl substituents. The meta and para have the greater commercial significance. All are colorless liquids.
What is the use of diethylbenzene?
The diethylbenzene is an inadvertent side product. Using shape-selective zeolite catalysts, the para isomer can be produced in high selectivity. Much diethylbenzene is recycled by transalkylation give ethylbenzene: Diethylbenzene is used in a mixture with methyl and/or ethyl biphenyls as a low temperature heat transfer fluid.
How is 1 2-diethylbenzene degraded in the atmosphere?
Vapor-phase 1,2-diethylbenzene will be degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals; the half-life for this reaction in air is estimated to be 2 days. 1,2-Diethylbenzene absorbs light in the environmental UV spectrum, and thus has the potential for direct photolysis.
