Answer:
The correct answer is 160.37 KJ/mol.
Explanation:
To find the activation energy in the given case, there is a need to use the Arrhenius equation, which is,
k = Ae^-Ea/RT
k1 = Ae^-Ea/RT1 and k2 = Ae^-Ea/RT2
k2/k1 = e^-Ea/R (1/T2-1/T1)
ln(k2/k1) = Ea/R (1/T1-1/T2)
The values of rate constant k1 and k2 are 3.61 * 10^-15 s^-1 and 8.66 * 10^-7 s^-1.
The temperatures T1 and T2 are 298 K and 425 K respectively.
Now by filling the values we get:
ln (8.66*10^-7/3.61*10^-15) = Ea/R (1/298-1/425)
19.29 = Ea/R * 0.001
Ea = 160.37 KJ/mol
Answer:
Sulfuric acid contains 2 hydrogen atoms, 1 sulfur atom, and 4 oxygen atoms.
Explanation:
Electrolysis takes place when an electric current passes through water.
<span>First, write the net ionic equation for the unbalanced reaction. If you are given a word equation to balance, you'll need to be able to identify strong electrolytes, weak electrolytes and insoluble compounds. Strong electrolytes completely dissociate into their ions in water. Examples of strong electrolytes are strong acids, strong bases, and soluble salts. Weak electrolytes yield very few ions in solution, so they are represented by their molecular formula (not written as ions). Water, weak acids, and weak bases are examples of weak electrolytes. The pH of a solution can cause them to dissociate, but in those situations, you'll be presented an ionic equation, not a word problem. Insoluble compounds do not dissociate into ions, so they are represented by the molecular formula. A table is provided to help you determine whether or not a chemical is soluble, but it's a good idea to memorize the solubility rules.
</span><span><span>arate the net ionic equation into the two half-reactions. This means identifying and separating the reaction into an oxidation half-reaction and a reduction half-reaction. </span><span>For one of the half-reactions, balance the atoms except for O and H. You want the same number of atoms of each element on each side of the equation. </span><span>Repeat this with the other half-reaction. </span><span>Add H2O to balance the O atoms. Add H+ to balance the H atoms. The atoms (mass) should balance out now. </span><span>Now balance charge. Add e- (electrons) to one side of each half-reaction to balance charge. You may need to multiply the electrons the the two half-reactions to get the charge to balance out. It's fine to change coefficients as long as you change them on both sides of the equation. </span><span>Now, add the two half-reactions together. Inspect the final equation to make sure it is balanced. Electrons on both sides of the ionic equation must cancel out. </span><span>Double-check your work! Make sure there are equal numbers of each type of atom on both sides of the equation. Make sure the overall charge is the same on both sides of the ionic equation. </span><span>If the reaction takes place in a basic solution, add an equal number of OH- as you have H+ ions. Do this for both sides of the equation and combine H+ and OH- ions to form H2O. </span><span>Be sure to indicate the state of each species. Indicate solid with (s), liquid for (l), gas with (g), and aqueous solution with (aq). </span><span>Remember, a balanced net ionic equation only describes chemical species that participate in the reaction. Drop additional substances from the equation.ExampleThe net ionic equation for the reaction you get mixing 1 M HCl and 1 M NaOH is:H+(aq) + OH-(aq) → H2O(l)Even though sodium and chlorine exist in the reaction, the Cl- and Na+ ions are not written in the net ionic equation because they don't participate in the reaction.</span></span>
Answer:
a. A reaction in which the entropy of the system increases can be spontaneous only if it is endothermic.
Explanation:
The change in free energy (ΔG) that is, the <u>energy available to do work</u>, of a system for a constant-temperature process is:
-
When ΔG < 0 the reaction is spontaneous in the forward direction.
- When ΔG > 0 the reaction is nonspontaneous. The reaction is
spontaneous in the opposite direction.
- When ΔG = 0 the system is at equilibrium.
If <u>both ΔH and ΔS are positive</u>, then ΔG will be negative only when the TΔS term is greater in magnitude than ΔH. This condition is met when T is large.
