Answer:
Regional metamorphic rocks form from other rocks (protoliths) by changes in mineralogy and texture in response to changing physical conditions (temperature, lithostatic pressure, and, in most cases, shear stress). Regional metamorphism occurs over broad areas in the lithosphere, possibly influenced by the heat supply. Regional metamorphic rock results from regional metamorphism and usually develops a flaky texture. These changes are essentially solid-state reactions, but very often a fluid phase is present, either participating in the reaction or as a reaction medium. Many regional metamorphic rocks have a chemical composition that is very similar to that of their sedimentary or igneous precursors, with the exception of removal or addition of volatiles (mainly H2O and CO2). This type of behavior is termed isochemical metamorphism. Metamorphism may also take place as a result of a change in chemical environment; this may occur by transport of elements between chemically contrasting rock types (e.g., formation of calc-silicate minerals at a quartzite–marble contact) or by circulation of fluids that dissolve some substances and precipitate others. This process of significant chemical change during metamorphism is known as allo-chemical metamorphism or metasomatism, and rocks formed in this manner are metasomatic rocks. Metasomatism is, however, mostly of local significance, and the total volume of metasomatic rocks in regional metamorphic terranes is rather minor. The distinction between metasomatism and is chemical metamorphism is also a matter of scale. On the scale of individual grains, mass transport takes place during all phase transformations; on the scale of a thin section, it is probably the rule for regional metamorphism; on the scale of a hand (sized) specimen, it can be observed frequently; and on a larger scale, it is the exception.
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The concentration of [H3O⁺]=2.86 x 10⁻⁶ M
<h3>Further explanation</h3>
In general, the weak acid ionization reaction
HA (aq) ---> H⁺ (aq) + A⁻ (aq)
Ka's value
![\large {\boxed {\bold {Ka \: = \: \frac {[H ^ +] [A ^ -]} {[HA]}}}}](https://tex.z-dn.net/?f=%5Clarge%20%7B%5Cboxed%20%7B%5Cbold%20%7BKa%20%5C%3A%20%3D%20%5C%3A%20%5Cfrac%20%7B%5BH%20%5E%20%2B%5D%20%5BA%20%5E%20-%5D%7D%20%7B%5BHA%5D%7D%7D%7D%7D)
Reaction
HC₂H₃O₂ (aq) + H₂O (l) ⇔ (aq) + H₃O⁺ (aq) Ka = 1.8 x 10⁻⁵
![\tt Ka=\dfrac{[C_2H_3O^{2-}[H_3O^+]]}{[HC_2H_3O_2]}}\\\\1.8\times 10^{-5}=\dfrac{0.22\times [H_3O^+]}{0.035}](https://tex.z-dn.net/?f=%5Ctt%20Ka%3D%5Cdfrac%7B%5BC_2H_3O%5E%7B2-%7D%5BH_3O%5E%2B%5D%5D%7D%7B%5BHC_2H_3O_2%5D%7D%7D%5C%5C%5C%5C1.8%5Ctimes%2010%5E%7B-5%7D%3D%5Cdfrac%7B0.22%5Ctimes%20%5BH_3O%5E%2B%5D%7D%7B0.035%7D)
[H₃O⁺]=2.86 x 10⁻⁶ M
Answer:
The charged carbon atom of a carbocation has a complete octet of valence shell electrons
Explanation:
A charged carbon atom of a carbocation has a valence shell that is not filled, <u>that's why it acts as an electrophile (or a Lewis base)</u>. This unfilled valence shell is also the reason of the nucleophilic attack that takes place during the second step of a SN1 reaction.
Answer:
whah the other dude said :) also stay safe
Explanation:
