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  2. Favorskii reaction - Wikipedia

    en.wikipedia.org/wiki/Favorskii_reaction

    HC≡CH + KOH ⇌ HC≡CK + H 2 O; RR'C=O + HC≡CK ⇌ RR'C(OK)C≡CH; The metal acetylide then reacts with an aldehyde or ketone to form a propargyl alcohol. When an α-hydrogen is present (as is the case when the carbonyl is an aldehyde), it will tautomerize to the corresponding enone. [4]

  3. Bromine compounds - Wikipedia

    en.wikipedia.org/wiki/Bromine_compounds

    Silver bromide (AgBr). Nearly all elements in the periodic table form binary bromides. The exceptions are decidedly in the minority and stem in each case from one of three causes: extreme inertness and reluctance to participate in chemical reactions (the noble gases, with the exception of xenon in the very unstable XeBr 2; extreme nuclear instability hampering chemical investigation before ...

  4. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    Reagents are "substances or compounds that are added to a system in order to bring about a chemical reaction or are added to see if a reaction occurs." [1] Some reagents are just a single element. However, most processes require reagents made of chemical compounds. Some of the most common ones used widely for specific reactive functions are ...

  5. Element–reactant–product table - Wikipedia

    en.wikipedia.org/wiki/Element–reactant...

    An element–reaction–product table is used to find coefficients while balancing an equation representing a chemical reaction. Coefficients represent moles of a substance so that the number of atoms produced is equal to the number of atoms being reacted with. [1] This is the common setup: Element: all the elements that are in the reaction ...

  6. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide used to study the massive deadenylation of adenine based-nucleosides induced by halogenated alkanes (alkyl halides) under physiological conditions. 2-Bromo-2-methylpropane causes the massive deguanylation of guanine based-nucleosides and massive deadenylation of adenine based-nucleosides.

  7. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    Structure of N-bromosuccinimide, a common brominating reagent in organic chemistry. Like the other carbon–halogen bonds, the C–Br bond is a common functional group that forms part of core organic chemistry. Formally, compounds with this functional group may be considered organic derivatives of the bromide anion.

  8. Equivalent (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Equivalent_(chemistry)

    The "hydrogen ion" and the "electron" in these examples are respectively called the "reaction units." By this definition, the number of equivalents of a given ion in a solution is equal to the number of moles of that ion multiplied by its valence. For example, consider a solution of 1 mole of NaCl and 1 mole of CaCl 2.

  9. Potassium bromide - Wikipedia

    en.wikipedia.org/wiki/Potassium_bromide

    Potassium bromide (K Br) is a salt, widely used as an anticonvulsant and a sedative in the late 19th and early 20th centuries, with over-the-counter use extending to 1975 in the US.