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  2. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.

  3. List of saturated fatty acids - Wikipedia

    en.wikipedia.org/wiki/List_of_saturated_fatty_acids

    Common Name Systematic Name Structural Formula Lipid Numbers Propionic acid: Propanoic acid CH 3 CH 2 COOH C3:0 Butyric acid: Butanoic acid CH 3 (CH 2) 2 COOH C4:0 Valeric acid: Pentanoic acid CH 3 (CH 2) 3 COOH C5:0 Caproic acid: Hexanoic acid CH 3 (CH 2) 4 COOH C6:0 Enanthic acid: Heptanoic acid CH 3 (CH 2) 5 COOH C7:0 Caprylic acid: Octanoic ...

  4. IUPAC nomenclature of organic chemistry - Wikipedia

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

    The alkyl (R') group is named first. The R−C(=O)O part is then named as a separate word based on the carboxylic acid name, with the ending changed from "-oic acid" to "-oate" or "-carboxylate" For example, CH 3 CH 2 CH 2 CH 2 COOCH 3 is methyl pentanoate, and (CH 3) 2 CHCH 2 CH 2 COOCH 2 CH 3 is ethyl 4-methylpentanoate.

  5. Propionic acid - Wikipedia

    en.wikipedia.org/wiki/Propionic_acid

    Propionic acid (/ p r oʊ p i ˈ ɒ n ɪ k /, from the Greek words πρῶτος : prōtos, meaning "first", and πίων : píōn, meaning "fat"; also known as propanoic acid) is a naturally occurring carboxylic acid with chemical formula CH 3 CH 2 CO 2 H. It is a liquid with a pungent and unpleasant smell somewhat resembling body odor. The ...

  6. Carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Carboxylic_acid

    Electron-withdrawing substituents, such as -CF 3 group, give stronger acids (the pK a of acetic acid is 4.76 whereas trifluoroacetic acid, with a trifluoromethyl substituent, has a pK a of 0.23). Electron-donating substituents give weaker acids (the pK a of formic acid is 3.75 whereas acetic acid, with a methyl substituent, has a pK a of 4.76)

  7. Butyric acid - Wikipedia

    en.wikipedia.org/wiki/Butyric_acid

    Butyric acid (/ ˈ b j uː t ɪ r ɪ k /; from Ancient Greek: βούτῡρον, meaning "butter"), also known under the systematic name butanoic acid, is a straight-chain alkyl carboxylic acid with the chemical formula CH 3 CH 2 CH 2 COOH. It is an oily, colorless liquid with an unpleasant odor. Isobutyric acid (2-methylpropanoic acid) is an ...

  8. Propylene - Wikipedia

    en.wikipedia.org/wiki/Propylene

    The industrial production of acrylic acid involves the catalytic partial oxidation of propylene. [19] Propylene is an intermediate in the oxidation to acrylic acid. In industry and workshops, propylene is used as an alternative fuel to acetylene in Oxy-fuel welding and cutting , brazing and heating of metal for the purpose of bending.

  9. Crotonaldehyde - Wikipedia

    en.wikipedia.org/wiki/Crotonaldehyde

    Crotonaldehyde is a chemical compound with the formula CH 3 CH=CHCHO. The compound is usually sold as a mixture of the E- and Z-isomers, which differ with respect to the relative position of the methyl and formyl groups.