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  2. Reactivity series - Wikipedia

    en.wikipedia.org/wiki/Reactivity_series

    The most reactive metals, such as sodium, will react with cold water to produce hydrogen and the metal hydroxide: 2 Na (s) + 2 H 2 O (l) →2 NaOH (aq) + H 2 (g) Metals in the middle of the reactivity series, such as iron , will react with acids such as sulfuric acid (but not water at normal temperatures) to give hydrogen and a metal salt ...

  3. Furan - Wikipedia

    en.wikipedia.org/wiki/Furan

    Diels-Alder reaction of furan with arynes provides corresponding derivatives of dihydronaphthalenes, which are useful intermediates in synthesis of other polycyclic aromatic compounds. [ 16 ] It is considerably more reactive than benzene in electrophilic substitution reactions, due to the electron-donating effects of the oxygen heteroatom.

  4. Electronegativities of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Electronegativities_of_the...

    See also: Electronegativities of the elements (data page) There are no reliable sources for Pm, Eu and Yb other than the range of 1.1–1.2; see Pauling, Linus (1960).

  5. Galvanic series - Wikipedia

    en.wikipedia.org/wiki/Galvanic_series

    The galvanic series (or electropotential series) determines the nobility of metals and semi-metals. When two metals are submerged in an electrolyte, while also electrically connected by some external conductor, the less noble (base) will experience galvanic corrosion. The rate of corrosion is determined by the electrolyte, the difference in ...

  6. 2,3-Dihydrofuran - Wikipedia

    en.wikipedia.org/wiki/2,3-Dihydrofuran

    The 2,3-dihydrofuran ring can be synthesized by several methods. These routes usually involve cyclization or cycloaddition reactions of carbonyl compounds using metal-containing catalysts. [5] [6] Iodine can also serve as a catalyst [7] as well as Raney nickel. [8]

  7. Borole - Wikipedia

    en.wikipedia.org/wiki/Borole

    The reaction with the electron-poor alkyne (C 6 F 5)CC(C 6 F 5) required rather harsh reaction conditions (110 °C, 7 days) and the only observable species was the expected Diels–Alder product (3), whose formation presumably follows a mechanism similar to that proposed for 5. The same pathway was found for the more electron-rich Et–CC–Et ...

  8. Aryne - Wikipedia

    en.wikipedia.org/wiki/Aryne

    In this method, the concerted mechanism of the Diels-Alder reaction between benzyne and furan is shown below. Other benzyne [4+2] cycloadditions are thought to proceed via a stepwise mechanism. A classic example is the synthesis of 1,2,3,4-tetraphenylnaphthalene . [ 27 ]

  9. List of chemical elements - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical_elements

    118 chemical elements have been identified and named officially by IUPAC.A chemical element, often simply called an element, is a type of atom which has a specific number of protons in its atomic nucleus (i.e., a specific atomic number, or Z).