Answer:
Sodium chloride solution:
First you need to calculate the mass of salt needed (done in the explanation), which is 58.44g. Then it have to be weighted in an analytical balance in a weighting boat and then transferred into a 2L volumetric flask that is going to be filled until the mark with distilled water.
Sulfuric acid dilution:
First you need to calculate the volume needed (done in the explanation), it is 16.6 mL. Using a graduated pipette one measures this volume and transfer it into a 2L volumetric flask that is already half filled with distilled water, and then one fills it until its mark.
Explanation:
Sodium chloride solution:
Each liter of a 0.500M solution has half mol, so 2L of said solution has 1 mol of salt. Sodium chloride molar mass is 58.44g/mol, so in 2L of solution there is 58.44g of salt. That`s the mass that`s going to be weighted and transferred to a 2L volumetric flask.
Sulfuric acid dilution:
This is the equation for dilution of solutions:
Where "c1" stands for the initial concentration (stock solution concentration), "v1" for the initial volume (volume of stock solution used), "c2" for the desired concentration and "v2" for the desired volume.
When we are diluting from a stock solution we want to know how much do we have to pipette from the stock solution into our volumetric flask. We do so by isolating the "v1" term from the dilution equation:
in this case that would be:
Answer:
(E) changing temperature
Explanation:
Consider the following reversible balanced reaction:
aA+bB⇋cC+dD
If we know the molar concentrations of each of the reaction species, we can find the value of Kc using the relationship:
Kc = ([C]^c * [D]^d) / ([A]^a * [B]^b)
where:
[C] and [D] are the concentrations of the products in the equilibrium; [A] and [B] reagent concentrations in equilibrium; already; b; c and d are the stoichiometric coefficients of the balanced equation. Concentrations are commonly expressed in molarity, which has units of moles / 1
There are some important things to remember when calculating Kc:
- <em>Kc is a constant for a specific reaction at a specific temperature</em>. If you change the reaction temperature, then Kc also changes
- Pure solids and liquids, including solvents, are not considered for equilibrium expression.
- The reaction must be balanced with the written coefficients as the minimum possible integer value in order to obtain the correct value of Kc
Answer:
4,38%
small molecular volumes
Decrease
Explanation:
The percent difference between the ideal and real gas is:
(47,8atm - 45,7 atm) / 47,8 atm × 100 = 4,39% ≈ <em>4,38%</em>
This difference is considered significant, and is best explained because argon atoms have relatively <em>small molecular volumes. </em>That produce an increasing in intermolecular forces deviating the system of ideal gas behavior.
Therefore, an increasing in volume will produce an ideal gas behavior. Thus:
If the volume of the container were increased to 2.00 L, you would expect the percent difference between the ideal and real gas to <em>decrease</em>
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I hope it helps!
Can you say please? Just kidding!
The process of science discovery depends upon changing your theories based upons new evidence from new experiments. New technology allows for new experiments, leading to new theories.
Answer:
-3.7771 × 10² kJ/mol
Explanation:
Let's consider the following equation.
3 Mg(s) + 2 Al³⁺(aq) ⇌ 3 Mg²⁺(aq) + 2 Al(s)
We can calculate the standard Gibbs free energy (ΔG°) using the following expression.
ΔG° = ∑np . ΔG°f(p) - ∑nr . ΔG°f(r)
where,
n: moles
ΔG°f(): standard Gibbs free energy of formation
p: products
r: reactants
ΔG° = 3 mol × ΔG°f(Mg²⁺(aq)) + 2 mol × ΔG°f(Al(s)) - 3 mol × ΔG°f(Mg(s)) - 2 mol × ΔG°f(Al³⁺(aq))
ΔG° = 3 mol × (-456.35 kJ/mol) + 2 mol × 0 kJ/mol - 3 mol × 0 kJ/mol - 2 mol × (-495.67 kJ/mol)
ΔG° = -377.71 kJ = -3.7771 × 10² kJ
This is the standard Gibbs free energy per mole of reaction.
