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  2. Weerman degradation - Wikipedia

    en.wikipedia.org/wiki/Weerman_degradation

    At first the carbonic acid amide (1) reacts with the sodium hypochlorite. After the separation of water and chloride an amine with a free bond is built 2. The intermediate (3) is generated by rearrangement. In the next step a hydrolysis takes place. Water is added at the carbon-atom with the number '1'. A hydroxylic group is generated.

  3. Dimethylacetamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylacetamide

    The chemical reactions of dimethylacetamide are typical of N,N-disubstituted amides. Hydrolysis of the acyl-N bond occurs in the presence of acids: CH 3 CON(CH 3) 2 + H 2 O + HCl → CH 3 COOH + (CH 3) 2 NH 2 + Cl −. However, it is resistant to bases. For this reason DMA is a useful solvent for reactions involving strong bases such as sodium ...

  4. Amide - Wikipedia

    en.wikipedia.org/wiki/Amide

    The core −C(=O)−(N) of amides is called the amide group (specifically, carboxamide group). In the usual nomenclature, one adds the term "amide" to the stem of the parent acid's name. For instance, the amide derived from acetic acid is named acetamide (CH 3 CONH 2). IUPAC recommends ethanamide, but this and related formal names are rarely ...

  5. N-(1-Naphthyl)ethylenediamine - Wikipedia

    en.wikipedia.org/wiki/N-(1-Naphthyl)ethylenediamine

    Then an excess but fixed volume of sulfanilamide and N-(1-naphthyl)ethylenediamine dihydrochloride solution is added. With nitrous acid as the limiting reagent, the azo coupling reaction produces an azo dye quantitatively with respect to the nitrite ions: The diazo compound formed accounts for the red coloration typical for a positive result.

  6. Hydroxylamine - Wikipedia

    en.wikipedia.org/wiki/Hydroxylamine

    Hydroxylamine derivatives substituted in place of the hydroxyl or amine hydrogen are (respectively) called O- or N‑hydroxyl­amines. In general N‑hydroxyl­amines are more common. Examples are N‑tert‑butyl­hydroxyl­amine or the glycosidic bond in calicheamicin. N,O‑Dimethyl­hydroxylamine is a precursor to Weinreb amides.

  7. Oxime - Wikipedia

    en.wikipedia.org/wiki/Oxime

    O-substituted oximes form a closely related family of compounds. Amidoximes are oximes of amides (R 1 C(=O)NR 2 R 3) with general structure R 1 C(=NOH)NR 2 R 3. Oximes are usually generated by the reaction of hydroxylamine with aldehydes (R−CH=O) or ketones (RR’C=O). The term oxime dates back to the 19th century, a combination of the words ...