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It is made by dissolving hydrogen bromide in water.
It is produced by treating sodium hydroxide with hydrogen bromide.
Breathing in gas with more than thirty parts per million of hydrogen bromide can be lethal to humans.
An investigation showed hydrogen bromide escaped when chemicals were wrongly mixed.
Hydrogen Bromide has been proposed for use in a utility-scale flow-type battery.
Bromine can be reduced by phosphorous acid to make hydrogen bromide.
Hydrogen bromide and hydrobromic acid are, therefore, not the same, but they are related.
It can also be made by reacting zinc with hydrogen bromide or hydrobromic acid.
Hydrogen bromide is even more toxic and irritating than hydrogen chloride.
Hydrogen bromide can also be used to convert alcohols to alkyl bromides.
The methoxyl-protecting groups of this intermediate are cleaved by hydrogen bromide giving dobutamine.
Hydrogen bromide is a chemical compound.
This reaction makes hydrogen bromide gas.
Chief McClain said that when hydrogen bromide was exposed to the air, it became an irritant to the eyes and skin.
It is manufactured for agricultural and industrial use by reacting methanol with hydrogen bromide:
Hydrogen bromide (along with hydrobromic acid) is produced on a much smaller scale than the corresponding chlorides.
TiBr hydrolyzes rapidly, potentially dangerously, to release hydrogen bromide.
Ammonium bromide can be prepared by the direct action of hydrogen bromide on ammonia.
It can also be prepared by the elimination of hydrogen bromide from bromostyrene using molten potassium hydroxide.
PhostrEx reacts very quickly with atmospheric moisture, breaking down into phosphorus acid and hydrogen bromide.
Bromine reacts with hydrogen in gaseous form and gives hydrogen bromide:
Metaldehyde is obtained in moderate yields by treatment of acetaldehyde with various acid catalysts, such as hydrogen bromide.
To illustrate, consider the alkoxy radical-catalyzed, anti-Markovnikov reaction of hydrogen bromide to an alkene.
This colorless liquid has a suffocating odor due to its tendency to hydrolyze with release of hydrogen bromide.
An alternative reaction is between protactinium pentachloride and hydrogen bromide or thionyl bromide.