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  • ...ens, allows them to substitute for halogens in several classes of chemical compounds. .../sub> || — || [[dinitrogen tetroxide]] || [[nitrous acid]] || nitrite || nitro- || -yl nitrite
    4 KB (399 words) - 20:19, 6 September 2022
  • | OtherNames = N-nitroguanidine<br>Nitro-guanidine<br>NQ<br>Picrite [[Category:Chemical compounds]]
    5 KB (594 words) - 22:43, 28 December 2020
  • ...ef> Sodium borate in glacial acetic acid will also oxidize oximes to nitro compounds. *Make aromatic nitro compounds
    6 KB (655 words) - 15:25, 30 November 2018
  • ...ts with an [[aldehyde]] or [[ketone]] in the presence of a base to form β-nitro alcohols, which can be further dehydrated to yield nitroalkenes, nitroketon ...36; (1903); p. 711</ref> DMDO can also be used to oxidize amines to nitro compounds.
    7 KB (850 words) - 22:48, 20 January 2020
  • ...ctional groups. For example, DMDO will oxidize primary [[amine]]s to nitro compounds and sulfides to sulfoxides. DMDO can also be used to convert nitro compounds to carbonyl compounds (Nef reaction).
    4 KB (481 words) - 12:00, 24 December 2022
  • Silver nitrite will react with haloalkanes to give nitro compounds. *Preparation of aniline compounds
    4 KB (426 words) - 22:05, 11 June 2023
  • ...ears prior that couples two carbonyl compounds to form β-hydroxy carbonyl compounds known as "aldols" (aldehyde and alcohol). ...he alkoxide by the previously protonated base will yield the respective β-nitro alcohol as product.
    2 KB (269 words) - 21:22, 10 August 2020
  • '''Nitro compounds''' are organic compounds that contain one or more nitro functional groups (−NO<sub>2</sub>). ...n be acidic. For similar reasons, the presence of nitro groups in aromatic compounds retards electrophilic aromatic substitution but facilitates nucleophilic ar
    6 KB (839 words) - 21:28, 26 October 2020
  • ...e esters of nitrous acid and contain the nitrosoxy functional group. Nitro compounds contain the C–NO<sub>2</sub> group. Nitrites have the general formula RON
    3 KB (473 words) - 00:51, 29 March 2020
  • Unlike other aromatic energetic compounds, styphnic acid cannot be safely burned as it may explode. [[Category:Chemical compounds]]
    6 KB (671 words) - 19:33, 16 May 2023
  • ...osive, based on the basic six-carbon [[benzene]] ring structure with three nitro functional groups (NO<sub>2</sub>) and three [[amine]] (NH<sub>2</sub>) gro Like nitroaromatic compounds, TATB is harmful if ingested and will stain the skin yellow.
    6 KB (753 words) - 22:08, 26 October 2020
  • [[Category:Chemical compounds]] [[Category:Organic compounds]]
    8 KB (913 words) - 19:47, 11 October 2020
  • ...o the public and when available it's more expensive than similar explosive compounds. *Make colored compounds
    5 KB (559 words) - 19:47, 25 October 2020
  • FOX-7 is a powerful explosive and like all nitro compounds it must be handled with care. [[Category:Chemical compounds]]
    8 KB (1,066 words) - 11:49, 28 December 2020
  • [[Category:Chemical compounds]] [[Category:Organic compounds]]
    4 KB (476 words) - 22:33, 28 December 2020
  • ...ide. As such, it does not reduce amides, ethers, lactones, nitriles, nitro compounds and epoxides. [[Category:Chemical compounds]]
    6 KB (625 words) - 21:17, 30 August 2022
  • | OtherNames = Penta-O-nitro-xylitol<br>XPN ...due to being a strong vasodilator, property seen in other nitrated organic compounds.
    6 KB (661 words) - 21:07, 31 August 2022
  • [[Category:Chemical compounds]] [[Category:Organic compounds]]
    5 KB (539 words) - 00:15, 6 November 2023

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