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  2. Click chemistry - Wikipedia

    en.wikipedia.org/wiki/Click_chemistry

    The above reaction occurs between a 1,2-aminothiol and a 2-cyanobenzothiazole to make luciferin, which is fluorescent. This luciferin fluorescence can be then quantified by spectrometry following a wash, and used to determine the relative presence of the molecule bearing the 1,2-aminothiol.

  3. Aqueous two-phase system - Wikipedia

    en.wikipedia.org/wiki/Aqueous_two-phase_system

    It is a common observation that when oil and water are poured into the same container, they separate into two phases or layers, because they are immiscible.In general, aqueous (or water-based) solutions, being polar, are immiscible with non-polar organic solvents (cooking oil, chloroform, toluene, hexane etc.) and form a two-phase system.

  4. Schreinemaker's analysis - Wikipedia

    en.wikipedia.org/wiki/Schreinemaker's_analysis

    Due to the phrasing of the Morey–Schreinemaker coincidence theorem, only one rule is essential to the Schreinemaker's rules. This is the so-called metastable extensions rule: [1] The metastable extension of the [phase-absent] reaction must fall in the sector in which that phase is stable in all possible assemblages.

  5. Reactive distillation - Wikipedia

    en.wikipedia.org/wiki/Reactive_distillation

    Moreover, the aqueous phase that forms after the condensation of the vapor is almost pure water. Depending on the requirement either of the phases can be withdrawn as a product and the other phase can be recycled back as reflux. The pure ester i.e. butyl acetate, being the least volatile component in the system, is realized as a bottom product.

  6. Azide-alkyne Huisgen cycloaddition - Wikipedia

    en.wikipedia.org/wiki/Azide-alkyne_Huisgen_cyclo...

    In the reaction above [4] azide 2 reacts neatly with alkyne 1 to afford the product triazole as a mixture of 1,4-adduct (3a) and 1,5-adduct (3b) at 98 °C in 18 hours. The standard 1,3-cycloaddition between an azide 1,3-dipole and an alkene as dipolarophile has largely been ignored due to lack of reactivity as a result of electron-poor olefins ...

  7. Heterogeneous catalysis - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_catalysis

    Hydrogenation of ethene on a catalytic solid surface (1) Adsorption (2) Reaction (3) Desorption. Heterogeneous catalysis is catalysis where the phase of catalysts differs from that of the reagents or products. [1] The process contrasts with homogeneous catalysis where the reagents, products and catalyst exist in the same phase.

  8. Catalysis - Wikipedia

    en.wikipedia.org/wiki/Catalysis

    The reaction occurs in two steps: 2 NO + O 22 NO 2 (rate-determining) NO 2 + SO 2 → NO + SO 3 (fast) The NO catalyst is regenerated. The overall rate is the rate of the slow step [14] v=2k 1 [NO] 2 [O 2]. An example of heterogeneous catalysis is the reaction of oxygen and hydrogen on the surface of titanium dioxide (TiO 2, or titania) to ...

  9. Sonogashira coupling - Wikipedia

    en.wikipedia.org/wiki/Sonogashira_coupling

    Some examples include: The coupling of 2-iodoprop-2-en-1-ol with a wide range of acetylenes. [52] The preparation of alk-2-ynylbuta-1,3-dienes from the cross-coupling of a diiodide and phenylacetylene, as shown below. [53] Synthesis of an alk-2-ynylbuta-1,3-diene accomplished by Sonogashira coupling. [53]

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