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  2. Methyl propiolate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propiolate

    Methyl propiolate is an organic compound with the formula HC 2 CO 2 CH 3. It is the methyl ester of propiolic acid , the simplest acetylenic carboxylic acid . It is a colorless liquid that is miscible with organic solvents.

  3. McCabe–Thiele method - Wikipedia

    en.wikipedia.org/wiki/McCabe–Thiele_method

    For the binary distillation depicted in Figure 1, the required number of theoretical plates is 6. Constructing a McCabe–Thiele diagram is not always straightforward. In continuous distillation with a varying reflux ratio, the mole fraction of the lighter component in the top part of the distillation column will decrease as the reflux ratio ...

  4. Methyl propionate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propionate

    Methyl propionate, also known as methyl propanoate, is an organic compound with the molecular formula CH 3 CH 2 CO 2 CH 3. It is a colorless liquid with a fruity, rum -like odor. [ 2 ]

  5. C4H4O2 - Wikipedia

    en.wikipedia.org/wiki/C4H4O2

    Methyl propiolate; Tetrolic acid This page was last edited on 1 October 2024, at 00:31 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...

  6. Category:Methyl esters - Wikipedia

    en.wikipedia.org/wiki/Category:Methyl_esters

    D. Daclatasvir; Damascenine; 4,21-Dehydrogeissoschizine; Dehydrosecodine; Demephion; Demeton-S-methyl; Desacetoxyvindoline; Deserpidine; Dexmethylphenidate; 3,4 ...

  7. Isobutane - Wikipedia

    en.wikipedia.org/wiki/Isobutane

    Since the longest continuous chain in isobutane contains only three carbon atoms, the preferred IUPAC name is 2-methylpropane but the locant (2-) is typically omitted in general nomenclature as redundant; C2 is the only position on a propane chain where a methyl substituent can be located without altering the main chain and forming the ...

  8. 1,3-Dipolar cycloaddition - Wikipedia

    en.wikipedia.org/wiki/1,3-Dipolar_cycloaddition

    The 1,3-dipolar cycloaddition is a chemical reaction between a 1,3-dipole and a dipolarophile to form a five-membered ring. The earliest 1,3-dipolar cycloadditions were described in the late 19th century to the early 20th century, following the discovery of 1,3-dipoles.

  9. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.