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The acid dissociation constant of bromous acid, K a = [H +][BrO − 2] / [HBrO 2] , was determined using different methods. The value of the pK a for bromous acid was estimated in research studying the decomposition of bromites. The research measured the rate of bromite decomposition as a function of hydrogen and bromite ion concentrations.
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 ...
Unlike chlorates, which very slowly disproportionate to chloride and perchlorate, the bromate anion is stable to disproportionation in both acidic and aqueous solutions. Bromic acid is a strong acid. Bromides and bromates may comproportionate to bromine as follows: [49] BrO − 3 + 5 Br − + 6 H + → 3 Br 2 + 3 H 2 O
Research papers from more than 55 disciplines Free & Subscription No Elsevier: HAL: Multidisciplinary: 760,000 (2,000,000 metadata) [14] An open-access database for French researchers. Organized into institution and domain portals. Free Yes CNRS's Centre pour la Communication Scientifique Directe (CCSD) RePEc: Research Papers in Economics [15 ...
Bromic acid, also known as hydrogen bromate, is an oxoacid with the molecular formula HBrO 3. It only exists in aqueous solution. [1] [2] It is a colorless solution that turns yellow at room temperature as it decomposes to bromine. [1] [3] Bromic acid and bromates are powerful oxidizing agents and are common ingredients in Belousov ...
Hypobromous acid is an inorganic compound with chemical formula of H O Br. It is a weak, unstable acid. It is mainly produced and handled in an aqueous solution. It is generated both biologically and commercially as a disinfectant. Salts of hypobromite are rarely isolated as solids.
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This definition was refined by Ronald Gillespie in 1971, as any acid with an H 0 value lower than that of 100% sulfuric acid (−11.93). [3] George A. Olah prepared the so-called " magic acid ", so named for its ability to attack hydrocarbons , by mixing antimony pentafluoride (SbF 5 ) and fluorosulfonic acid (FSO 3 H). [ 4 ]