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  2. 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 ...

  3. Amino radical - Wikipedia

    en.wikipedia.org/wiki/Amino_radical

    In chemistry, the amino radical, ·NH 2, also known as the aminyl or azanyl, is the neutral form of the amide ion (NH − 2). Aminyl radicals are highly reactive and consequently short-lived, like most radicals; however, they form an important part of nitrogen chemistry. In sufficiently high concentration, amino radicals dimerise to form hydrazine.

  4. Amide (functional group) - Wikipedia

    en.wikipedia.org/wiki/Amide_(functional_group)

    Structures of three kinds of amides: an organic amide (carboxamide), a sulfonamide, and a phosphoramide. In chemistry, the term amide (/ ˈ æ m aɪ d / or / ˈ æ m ɪ d / or / ˈ eɪ m aɪ d /) [1] [2] [3] is a compound with the functional group R n E(=O) x NR 2, where x is not zero, E is some element, and each R represents an organic group or hydrogen. [4]

  5. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    The two major resonance forms of an amide. Another factor that plays a role in determining the reactivity of acyl compounds is resonance. Amides exhibit two main resonance forms. Both are major contributors to the overall structure, so much so that the amide bond between the carbonyl carbon and the amide nitrogen has significant double bond ...

  6. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    Amide Polar Neutral −3.5 132.119 3.93 AAY Aspartate: Asp D Anion Brønsted base: Negative −3.5 133.104 5.49 GAY Cysteine: Cys C Thiol Brønsted acid Neutral 2.5 250 0.3 121.154 1.38 UGY Glutamine: Gln Q Amide Polar Neutral −3.5 146.146 3.9 CAR Glutamate: Glu E Anion Brønsted base Negative −3.5 147.131 6.32 GAR Glycine: Gly G Aliphatic ...

  7. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    The Hofmann rearrangement (Hofmann degradation) is the organic reaction of a primary amide to a primary amine with one less carbon atom. [1] [2] [3] The reaction involves oxidation of the nitrogen followed by rearrangement of the carbonyl and nitrogen to give an isocyanate intermediate.

  8. The worst foods to buy in the supermarket and the better ...

    www.aol.com/worst-foods-buy-supermarket-better...

    Health experts recommend reducing a person's intake of ultra-processed foods. A registered dietitian and the CEO of Nourish Science share some helpful ways to spot these foods where you shop.

  9. Neutralization (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Neutralization_(chemistry)

    Animation of a strong acid–strong base neutralization titration (using phenolphthalein).The equivalence point is marked in red. In chemistry, neutralization or neutralisation (see spelling differences) is a chemical reaction in which acid and a base react with an equivalent quantity of each other.