enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 2-Nitrochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/2-Nitrochlorobenzene

    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% nitric acid, 56% sulfuric acid and 14% water, the product mix is typically 34-36% 2-nitrochlorobenzene and 63-65% 4-nitrochlorobenzene , with only about 1% 3-nitrochlorobenzene .

  3. Nitro compound - Wikipedia

    en.wikipedia.org/wiki/Nitro_compound

    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 ...

  4. Nucleophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_aromatic...

    The following is the reaction mechanism of a nucleophilic aromatic substitution of 2,4-dinitrochlorobenzene (1) in a basic solution in water. Nucleophilic aromatic substitution Since the nitro group is an activator toward nucleophilic substitution, and a meta director, it is able to stabilize the additional electron density (via resonance) when ...

  5. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    Chlorobenzene once was used in the manufacture of pesticides, most notably DDT, by reaction with chloral (trichloroacetaldehyde), but this application has declined with the diminished use of DDT. At one time, chlorobenzene was the main precursor for the manufacture of phenol: [10] C 6 H 5 Cl + NaOH → C 6 H 5 OH + NaCl

  6. 3-Nitrochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/3-Nitrochlorobenzene

    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 ...

  7. Birkeland–Eyde process - Wikipedia

    en.wikipedia.org/wiki/Birkeland–Eyde_process

    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]

  8. Nitric-oxide reductase - Wikipedia

    en.wikipedia.org/wiki/Nitric-oxide_reductase

    Nitric oxide reductase reduces NO to N 2 O. Nitric oxide reductase belongs to the family of oxidoreductases, specifically those acting on other nitrogenous compounds as donors with other acceptors. The systematic name of this enzyme class is nitrous-oxide:acceptor oxidoreductase (NO-forming). Other names in common use include nitrogen oxide ...

  9. Hydroformylation - Wikipedia

    en.wikipedia.org/wiki/Hydroformylation

    In the case of dicobalt octacarbonyl or Co 2 (CO) 8 as a catalyst, pentan-3-one can arise from ethene and CO, in the absence of hydrogen. A proposed intermediate is the ethylene-propionyl species [CH 3 C(O)Co(CO) 3 (ethene)] which undergoes a migratory insertion to form [CH 3 COCH 2 CH 2 Co(CO) 3]. The required hydrogen arises from the water ...