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  2. 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 ...

  3. 2,4-Dinitrochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrochlorobenzene

    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 important intermediate for the industrial production of other compounds. [2] DNCB is produced commercially by the nitration of p-nitrochlorobenzene with a mixture of nitric and ...

  4. 2,4-Dinitrophenol - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenol

    2,4-Dinitrophenol (2,4-DNP or simply DNP) is an organic compound with the formula HOC 6 H 3 (NO 2) 2. It has been used in explosives manufacturing and as a pesticide and herbicide. In humans, DNP causes dose-dependent mitochondrial uncoupling , causing the rapid loss of ATP as heat and leading to uncontrolled hyperthermia —up to 44 °C (111 ...

  5. Dinitrophenol - Wikipedia

    en.wikipedia.org/wiki/Dinitrophenol

    There are six isomers of dinitrophenol: Chemical structure of 2,4-Dinitrophenol. 2,3-Dinitrophenol; 2,4-Dinitrophenol; 2,5-Dinitrophenol; 2,6-Dinitrophenol; 3,4-Dinitrophenol; 3,5-Dinitrophenol; Dinitrophenols also form the core structure of some herbicides, which are collectively referred to as dinitrophenol herbicides, including: Chemical ...

  6. Dinitrobenzene - Wikipedia

    en.wikipedia.org/wiki/Dinitrobenzene

    The three possible arrangements of the nitro groups afford three isomers, 1,2-dinitrobenzene, 1,3-dinitrobenzene, and 1,4-dinitrobenzene. Each isomer has the chemical formula C 6 H 4 N 2 O 4 and a molar mass of about 168.11 g/mol. 1,3-Dinitrobenzene is the most common isomer and it is used in the manufacture of explosives .

  7. Nitrophenol - Wikipedia

    en.wikipedia.org/wiki/Nitrophenol

    2,4-dinitrophenol picric acid 2,4-Dinitrophenol (m.p. 83 °C) is a moderately strong acid (pK a = 4.89). 2,4,6-Trinitrophenol is better known as picric acid , which has a well-developed chemistry.

  8. 7 Cognacs for Sipping, Mixing Into Cocktails, and Gifting ...

    www.aol.com/7-cognacs-sipping-mixing-cocktails...

    December 6, 2024 at 3:00 PM. ... And unlike most other spirits, Cognacs can be aged in both dry and humid cellars; in the former, more water evaporates through the porous wood staves, which leaves ...

  9. 2,4-Dinitrophenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenylhydrazine

    2,4-Dinitrophenylhydrazine (2,4-DNPH or DNPH) is the organic compound C 6 H 3 (NO 2) 2 NHNH 2. DNPH is a red to orange solid. It is a substituted hydrazine. The solid is relatively sensitive to shock and friction. For this reason DNPH is usually handled as a wet powder. DNPH is a precursor to the drug Sivifene.