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  2. 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 ...

  3. Infrared spectroscopy correlation table - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy...

    esters and lactones: 1735 influenced by conjugation and ring size (as with ketones) anhydrides 1760 1820 acyl halides: 1800 amides: 1650 associated amides carboxylates (salts) 1550–1610 amino acid zwitterions 1550–1610 O─H alcohols, phenols: low concentration 3610–3670 high concentration 3200–3400 broad carboxylic acids low concentration

  4. Ester - Wikipedia

    en.wikipedia.org/wiki/Ester

    An ester of a carboxylic acid. R stands for any group (typically hydrogen or organyl) and R ′ stands for any organyl group. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (R ′). [1]

  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. Amide - Wikipedia

    en.wikipedia.org/wiki/Amide

    The solubilities of amides and esters are roughly comparable. Typically amides are less soluble than comparable amines and carboxylic acids since these compounds can both donate and accept hydrogen bonds. Tertiary amides, with the important exception of N,N-dimethylformamide, exhibit low solubility in water.

  7. Category:Esters - Wikipedia

    en.wikipedia.org/wiki/Category:Esters

    In organic chemistry and biochemistry esters are the functional group (R'-COOR") consisting of an organic radical united with the residue of any oxygen acid, either organic or inorganic. An ester is a product of the reaction of an acid (usually organic) and an alcohol (the hydrogen of the acid R-COOH is replaced by an alkyl group R").

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  9. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    an organoaluminium compound ; a reducing agent; converts esters and nitriles to aldehydes Diisopropyl azodicarboxylate: the diisopropyl ester of azodicarboxylic acid; a reagent in the production of many organic compounds Dimethyl ether: the simplest ether; a useful precursor to other organic compounds and an aerosol propellant: Dimethylformamide