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In chemistry, the term chemically inert is used to describe a substance that is not chemically reactive. From a thermodynamic perspective, a substance is inert, or nonlabile, if it is thermodynamically unstable (positive standard Gibbs free energy of formation) yet decomposes at a slow, or negligible rate. [1]
In 1902, having accepted the evidence for the elements helium and argon, Dmitri Mendeleev included these noble gases as group 0 in his arrangement of the elements, which would later become the periodic table. [11] Ramsay continued his search for these gases using the method of fractional distillation to separate liquid air into several components.
The Group 1 metal (M) is oxidised to its metal ions, and water is reduced to hydrogen gas (H 2) and hydroxide ion (OH −), giving a general equation of: 2 M(s) + 2 H 2 O(l) 2 M + (aq) + 2 OH − (aq) + H 2 (g) [8] The Group 1 metals or alkali metals become more reactive as their number of energy levels inceases.
The most reactive kind of metallic element is an alkali metal of group 1 (e.g., sodium or potassium); this is because such an atom has only a single valence electron. During the formation of an ionic bond , which provides the necessary ionization energy , this one valence electron is easily lost to form a positive ion (cation) with a closed ...
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Argon is used in some high-temperature industrial processes where ordinarily non-reactive substances become reactive. For example, an argon atmosphere is used in graphite electric furnaces to prevent the graphite from burning. For some of these processes, the presence of nitrogen or oxygen gases might cause defects within the material.
Reactive dogs can be tricky to manage, whether your own dog struggles with reactivity or you and your pup have encountered other reactive dogs when you’re out and about. But reactivity isn’t ...
Highly favourable binding of a substrate at a non-reactive site will force the reactive site of the substrate to be more reactive by putting it in a very unfavourable position. [3] This effect was observed in orotidine 5‘-phosphate decarboxylase . [ 4 ]