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In organic synthesis, PPTS is used as a weakly acidic catalyst, providing an organic soluble source of pyridinium (C 5 H 5 NH +) ions.For example, PPTS is used to deprotect silyl ethers or tetrahydropyranyl ethers when a substrate is unstable to stronger acid catalysts.
An electrically operated water pump is the prime motivator in recirculating the water from the pool. Water is forced through a filter and then returned to the pool. Using a water pump by itself is often not sufficient to completely sanitize a pool. Commercial and public pool pumps usually run 24 hours a day for the entire operating season of ...
Salt water chlorination is a process that uses dissolved salt (1000–4000 ppm or 1–4 g/L) for the chlorination of swimming pools and hot tubs.The chlorine generator (also known as salt cell, salt generator, salt chlorinator, or SWG) uses electrolysis in the presence of dissolved salt to produce chlorine gas or its dissolved forms, hypochlorous acid and sodium hypochlorite, which are already ...
Pool-type reactor can mean: A water-cooled Swimming pool reactor; A Sodium-cooled fast reactor of the pool rather than loop type This page was last edited on 4 ...
Stock tanks can be repurposed as backyard pools, or "stock tank pools," using chlorine tabs and a filter pump. Stock tanks are increasingly used as "rustic" backyard above-ground pools, or "stock tank pools" by retrofitting a filter pump [4] and adding chlorine or stabilized hydrogen peroxide [5] to keep the water clean throughout the summer. [6]
2-Picoline was the first pyridine compound reported to be isolated in pure form. It was isolated from coal tar in 1846 by T. Anderson. [2] This chemistry was practiced by Reilly Industries. [3] It is now mainly produced by two principal routes. One method involves the condensation of acetaldehyde and ammonia in the presence of an oxide catalyst ...
With secondary amines and not primary amines the Zincke reaction takes on a different shape forming so-called Zincke aldehydes in which the pyridine ring is ring-opened with the terminal iminium group hydrolyzed to an aldehyde: [4] Zincke aldehydes. This variation has been applied in the synthesis of novel indoles: [11] Zincke aldehydes Kearney ...
Using secondary amines (as opposed to primary amines) the Zincke reaction takes on a different shape forming Zincke aldehydes in which the pyridine ring is ring-opened with the terminal iminium group hydrolyzed to an aldehyde. The use of the dinitrophenyl group for pyridine activation was first reported by Theodor Zincke.