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2-Nitrochlorobenzene is an organic compound with the formula ClC 6 H 4 NO 2. It is one of three isomeric nitrochlorobenzenes . [ 1 ] It is a yellow crystalline solid that is important as a precursor to other compounds due to its two functional groups.
Explosive decomposition of organo nitro compounds are redox reactions, wherein both the oxidant (nitro group) and the fuel (hydrocarbon substituent) are bound within the same molecule. The explosion process generates heat by forming highly stable products including molecular nitrogen (N 2), carbon dioxide, and water. The explosive power of this ...
Due to relatively weak N–O bonding, all nitrogen oxides are unstable with respect to N 2 and O 2, which is the principle behind the catalytic converter, and prevents the oxygen and nitrogen in the atmosphere from combusting.
2,4-Dinitrochlorobenzene (DNCB) is an organic compound with the chemical formula (O 2 N) 2 C 6 H 3 Cl. It is a yellow solid that is soluble in organic solvents . It is an intermediate for the industrial production of other compounds.
In this biological process, which is a redox comproportionation reaction, nitrite and ammonium ions are converted directly into a diatomic molecule of nitrogen and water. [8] NH + 4 + NO − 2 → N 2 + 2 H 2 O (ΔG° = −357 kJ⋅mol −1). [9] Globally, this process may be responsible for 30–50% of the N 2 gas produced in the oceans. [10]
Nitrochlorobenzene is typically synthesized by nitration of chlorobenzene in the presence of sulfuric acid: C 6 H 5 Cl + HNO 3 → O 2 NC 6 H 4 Cl + H 2 O. This reaction affords a mixture of isomers. Using an acid ratio of 30/56/14, the product mix is typically 34-36% 2-nitrochlorobenzene and 63-65% 4-nitrochlorobenzene, with only about 1% 3 ...
The Birkeland–Eyde process was one of the competing industrial processes in the beginning of nitrogen-based fertilizer production. It is a multi-step nitrogen fixation reaction that uses electrical arcs to react atmospheric nitrogen (N 2) with oxygen (O 2), ultimately producing nitric acid (HNO 3) with water. [1]
For example, the industrial production of chloroethane proceeds by the reaction of ethylene with HCl: H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 1 ⁄ 2 O 2 → ClCH 2 CH 2 Cl + H 2 O.