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An early example is the dialkylation of a nickel dithiolate: [2] The corresponding alkylation in the absence of a metal ion would yield polymers. Crown ethers arise from dialkylations that are templated by alkali metals. [3] Other template reactions include the Mannich and Schiff base condensations. [4]
For example, if the reaction equation had 2 H + ions in the product, then the "change" for that cell would be "2x" The fourth row, labeled E, is the sum of the first two rows and shows the final concentrations of each species at equilibrium. It can be seen from the table that, at equilibrium, [H +] = x.
If the template has a separate documentation page (usually called "Template:template name/doc"), add [[Category:Chemistry formatting and function templates]] to the <includeonly> section at the bottom of that page. Otherwise, add <noinclude>[[Category:Chemistry formatting and function templates]]</noinclude>
a strong base used in organic synthesis Sodium hydroxide: strong base with many industrial uses; in the laboratory, used with acids to produce the corresponding salt, also used as an electrolyte: Sodium hypochlorite: frequently used as a disinfectant or a bleaching agent Sodium nitrite: used to convert amines into diazo compounds Sulfuric acid
2-tert-Butyl-1,1,3,3-tetramethylguanidine is an organic base, also known as Barton's base. It is named after Nobel Prize-winning British chemist Derek Barton . Barton and his assistants prepared a series of guanidines with steric hindrance in 1982; in this case five alkyl groups : four methyl groups and one tert -butyl group .
In a buffer, a weak acid and its conjugate base (in the form of a salt), or a weak base and its conjugate acid, are used in order to limit the pH change during a titration process. Buffers have both organic and non-organic chemical applications. For example, besides buffers being used in lab processes, human blood acts as a buffer to maintain pH.
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