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The oxidation state, sometimes referred to as oxidation number, describes the degree of oxidation of an atom in a chemical compound.
<u>Explanation:</u>
The oxidation number of an atom is the charge that atom would have if the compound was composed of ions. 1. The oxidation number of an atom is zero in a neutral substance that contains atoms of only one element. The oxidation number of simple ions is equal to the charge on the ion.
The oxidation number of a mono atomic ion equals the charge of the ion. The oxidation number of H is +1, but it is -1 in when combined with less electro negative elements. The oxidation number of O in compounds is usually -2, but it is -1 in peroxides. The oxidation number of a Group 1 element in a compound is +1.
Answer:
35.1 kJ/mol is the expected value for the heat of sublimation of acetic acid.
Explanation:
..[1]
Heat of vaporization of acetic acid = 
..[2]
Heat of fusion of acetic acid = 
Heat of sublimation of acetic acid = 
..[3]
[1] + [2] = [3] (Hess's law)


35.1 kJ/mol is the expected value for the heat of sublimation of acetic acid.
Addition of water to an alkyne gives a keto‑enol tautomer product and that is the product changed into 2-pentanone, then the alkyne need to had been 1-pentyne. 2-pentyne might have given a combination of 2- and 3-pentanone.
<h3>
What is the keto-enol means in tautomer?</h3>
They carries a carbonyl bond even as enol implies the presence of a double bond and a hydroxyl group. The keto-enol tautomerization equilibrium is depending on stabilization elements of each the keto tautomer and the enol tautomer.
- The enol that could provide 2-pentanone might had been pent-1- en - 2 -ol. Because an equilibrium favors the ketone so greatly, equilibrium isn't an excellent description.
- If the ketone have been handled with bromine, little response might be visible because the enol content material might be too low.
- If a catalyst have been delivered, NaOH for example, then formation of the enolate of pent-1-en - 2 - ol might shape and react with bromine.
- This might finally provide a bromoform product. Under acidic conditions, the enol might desire formation of the greater substituted enol constant with alkene stability.