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  2. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The shorter of the two chains becomes the first part of the name with the -ane suffix changed to -oxy, and the longer alkane chain becomes the suffix of the name of the ether. Thus, CH 3 OCH 3 is methoxymethane, and CH 3 OCH 2 CH 3 is methoxyethane ( not ethoxymethane).

  3. 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 ...

  4. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    These possibilities have been used to account for the fact that, for certain substrates like α-tetralone, the group that migrates can sometimes change, depending on the conditions used, to deliver either of the two possible amides. [8] Two proposed reaction mechanisms for the amide formation from a ketone via Schmidt reaction

  5. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    According to some authors, organyl derivatives of acidic hydrogen of other acids are esters as well (e.g. amides), but not according to the IUPAC. [ 1 ] An example of an ester formation is the substitution reaction between a carboxylic acid ( R−C(=O)−OH ) and an alcohol (R'OH), forming an ester ( R−C(=O)−O−R' ), where R and R′ are ...

  6. 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.

  7. Category:Amides - Wikipedia

    en.wikipedia.org/wiki/Category:Amides

    Amides are the members of a group of organic chemical compounds containing nitrogen. Specifically, an amide results from an acid , in which a carbon atom is double bonded to oxygen and also to a hydroxyl group, when the hydroxyl group is replaced by an amine .

  8. Today’s NYT ‘Strands’ Hints, Spangram and Answers ... - AOL

    www.aol.com/today-nyt-strands-hints-spangram...

    We'll cover exactly how to play Strands, hints for today's spangram and all of the answers for Strands #344 on Monday, February 10. Related: 16 Games Like Wordle To Give You Your Word Game Fix ...

  9. 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]