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Chemiluminescence was first observed with lophine (triphenylimidazole). [2] When in basic solution, this compound converts to the imidazolate, which reacts with oxygen to eventually give a dioxetane. Fragmentation of the dioxetane gives the excited state of an anionic diamide. [3] Steps leading up to chemiluminescence of lophine.
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 ...
Reagent test Alcohols: Forms Lucas test in alcohols is a test to differentiate between primary, secondary, and tertiary alcohols. Alkaloids: Forms Froehde Liebermann Mandelin Marquis Mayer's Mecke Simon's: Amines, and amino acids: Forms Folin's: Barbiturates: Class Dille–Koppanyi Zwikker: Benzodiazepines: Class Zimmermann: Phytocannabinoids ...
The sensitivity of the reagent may become altered after the recommended time period. [11] Microtox Osmotic Adjustment Solution (MOAS) is a nontoxic solution that is made up of 22% sodium chloride and ultra-pure water. This solution is added to a sample to adjust the osmotic pressure to approximately 2% NaCl. [11]
Schweizer's reagent was once used in production of cellulose products such as rayon and cellophane (see cupro). Cellulose, which is quite insoluble in water (hence its utility as clothing), dissolves in the presence of Schweizer's reagent. Using the reagent, cellulose can be extracted from wood pulp, cotton fiber, and other natural cellulose ...
Schwartz's reagent is the common name for the organozirconium compound with the formula (C 5 H 5) 2 ZrHCl, sometimes called zirconocene hydrochloride or zirconocene chloride hydride, and is named after Jeffrey Schwartz, a chemistry professor at Princeton University.
The main difference between solution (1) and solution (2) is the different use of nitrate-nitrogen and ammonium-nitrogen based stock solutions to prepare the respective Hoagland solution of interest. Accordingly, the original 1933 and the modified concentrations of 1938 and 1950 for each essential element and sodium are shown below, the ...
Currently, Rosenthal's reagent is often used instead of Negishi's reagent (1-butene)zirconocene to generate zirconocene fragments as it offers a number of compelling advantages. Unlike Negishi's reagent, Rosenthal's reagent is stable at room temperature and can be stored indefinitely under an inert atmosphere.