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  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. Element–reactant–product table - Wikipedia

    en.wikipedia.org/wiki/Element–reactant...

    An element–reaction–product table is used to find coefficients while balancing an equation representing a chemical reaction. Coefficients represent moles of a substance so that the number of atoms produced is equal to the number of atoms being reacted with. [1] This is the common setup: Element: all the elements that are in the reaction ...

  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. Heterogeneous water oxidation - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_Water_Oxidation

    2H 2 O → O 2 + 4H + + 4e − Oxidation (generation of dioxygen) 4H + + 4e − → 2H 2 Reduction (generation of dihydrogen) 2H 2 O → 2H 2 + O 2 Total Reaction Of the two half reactions, the oxidation step is the most demanding because it requires the coupling of 4 electron and proton transfers and the formation of an oxygen-oxygen bond.

  6. Ammonolysis - Wikipedia

    en.wikipedia.org/wiki/Ammonolysis

    Ammonolysis reactions can be conducted with organic compounds to produce amines (molecules containing a nitrogen atom with a lone pair, :N), [2] or with inorganic compounds to produce nitrides. [3] [4] This reaction is analogous to hydrolysis in which water molecules are split.

  7. On-water reaction - Wikipedia

    en.wikipedia.org/wiki/On-water_reaction

    The reaction of quadricyclane with DEAD is a 2σ + 2σ + 2π cycloaddition that on water takes place within 10 minutes at room temperature with 82% yield. The same reaction in toluene takes 24 hours at 80 °C with 70% yield. An emulsion reaction in fluorinated cyclohexane takes 36 hours and the neat reaction takes even longer (48 hours).

  8. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    Chlorobenzene has been detected in a sedimentary rock on Mars. [13] It was speculated that the chlorobenzene might have been produced when the sample was heated in the instrument sampling chamber. The heating would have triggered a reaction of organics in the Martian soil, which is known to contain perchlorate.

  9. 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 ...

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