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Answer:
b) Both p orbitals are perpendicular to the F−Be−F bond axes.
Explanation:
Be has 2 electrons in its valence shell, subshell s is fulfilled, so it has no unpaired electrons in its ground state to make bonds with F. So, it can promote the electrons to the 2p orbital and will having sp hybridization.
The bond between the orbitals sp and the p orbital of F are in opposite directions but the same ax. The two bonds are equivalent, and the molecule had a linear geometry. The two unhybridized p orbitals on Be are vacant, and so they are perpendicular to the F-Be-F bond axes.
The balanced chemical equation for the above reaction is as follows ;
Mg + 2HCl —> MgCl2 + H2
The stoichiometry of Mg to HCl is 1:2
This means that 1 mol of Mg reacts with 2 mol of HCl
Equal amounts of both Mg and HCl have been added. One reagent is the limiting reactant and other reactant is in excess.
Limiting reactant is the reagent that is fully used up in the reaction and the amount of Product formed depends on the amount of limiting reactant present.
In this reaction if Mg is the limiting reactant, 4.40 moles of Mg should react with 4.40x2 -8.80 moles of HCl.
But only 4.40 moles of HCl present therefore HCl is the limiting reactant that reacts with 4.40/2 = 2.20 moles of Mg
Stoichiometry of HCl to MgCl2 is 2:1
Since HCl moles reacted -4.40 mol
Then MgCl2 moles formed are 4.40/2 = 2.20 mol of MgCl2
Answer:
2.29x10⁻¹² is Ksp of the salt
Explanation:
The Ksp of the metal hydroxide is:
M(OH)₂(s) ⇄ M²⁺ + 2OH⁻
Ksp = [M²⁺] [OH⁻]²
As you can see in the reaction, 2 moles of OH⁻ are produced per mole of M²⁺. It is possible to find [OH⁻] with pH, thus:
pOH = 14- pH
pOH = 14 - 10.22
pOH = 3.78
pOH = -log[OH⁻]
<em>1.66x10⁻⁴ = [OH⁻]</em>
And [M²⁺] is the half of [OH⁻], <em>[M²⁺] = 8.30x10⁻⁵</em>
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Replacing in Ksp formula:
Ksp = [8.30x10⁻⁵] [1.66x10⁻⁴]²
Ksp = 2.29x10⁻¹² is Ksp of the salt
Answer:
See explanation and image attached
Explanation:
Here attached are resonance forms of pyrrole and pyridine. The images were obtained from quora and researchgate respectively.
Now, we can see that in the resonance forms of pyrrole, the nitrogen atom in the heterocycle has a formal charge of +1. However, in the six membered pyridine hetrocycle, the nitrogen atom may have a formal charge of -1 or +1 as shown in the canonical structures attached. The structures in which nitrogen has a +1 formal charge in pyridine are comparable to structures obtained from pyrrole. These structures have less contribution to the structure of pyridine.