Which would have the highest first ionization energy?
2 answers:
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Answer:
C) 0.800 mol
Explanation:
- 4Al + 3O₂ → 2Al₂O₃
In order to <u>convert from moles of Al₂O₃ into moles of Al</u>, we'll need to use<em> the stoichiometric coefficients</em>, using a conversion factor that has Al₂O₃ moles in the denominator and Al moles in the numerator:
- 0.400 mol Al₂O₃ *
= 0.800 mol Al
So the correct answer is option C).
Taking into account the reaction stoichiometry, 2.13 grams of magnesium was dissolved in the solution.
<h3>Reaction stoichiometry</h3>In first place, the balanced reaction is:
Mg²⁺(aq) + Na₂CO₃(aq) → MgCO₃(s) + 2 Na⁺(aq)
By reaction stoichiometry (that is, the relationship between the amount of reagents and products in a chemical reaction), the following amounts of moles of each compound participate in the reaction:
- Mg²⁺: 1 mole
- Na₂CO₃: 1 mole
- MgCO₃: 1 mole
- Na⁺: 2 moles
The molar mass of the compounds is:
- Mg²⁺: 24.3 g/mole
- Na₂CO₃: 106 g/mole
- MgCO₃: 84.3 g/mole
- Na⁺: 23 g/mole
Then, by reaction stoichiometry, the following mass quantities of each compound participate in the reaction:
- Mg²⁺: 1 mole ×24.3 g/mole= 24.3 grams
- Na₂CO₃: 1 mole ×106 g/mole= 106 grams
- MgCO₃: 1 mole ×84.3 g/mole=84.3 grams
- Na⁺: 2 moles ×23 g/mole= 46 grams
The following rule of three can be applied: If by reaction stoichiometry 1 mole of Na₂CO₃ react with 24.3 grams of magnesium, 0.0877 moles of Na₂CO₃ react with how much mass of magnesium?
<u><em>mass of magnesium= 2.13 grams</em></u>
Finally, 2.13 grams of magnesium was dissolved in the solution.
Learn more about the reaction stoichiometry:
<span>1,3-cylohexadiene i synthesized starting from cyclohexane in following 4 steps.
1) Free Radical Substitution Rxn: Halogenation of cyclohexane in the presence of UV yield chlorocyclohexane.
2) Elimination Rxn: Dehydrohalogenation of chlorocyclohexane yields cyclohexene.
3) Halogenation of Cyclohexene (Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
4) Elemination Rxn: When dibromocyclohexane is treated with KOH and heated it gives 1,3-cyclohexadiene as shown below,</span>
1) Free Radical Substitution Rxn: Halogenation of cyclohexane in the presence of UV yield chlorocyclohexane.
2) Elimination Rxn: Dehydrohalogenation of chlorocyclohexane yields cyclohexene.
3) Halogenation of Cyclohexene (Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
4) Elemination Rxn: When dibromocyclohexane is treated with KOH and heated it gives 1,3-cyclohexadiene as shown below,</span>