Answer:
Oxygen is oxidized and hydrogen is reduced.
Explanation:
Let's consider the redox reaction during the electrolysis of water in an electrolytic cell.
2 H₂O ⇒ 2 H₂ + O₂
The corresponding half-reactions are:
2 e⁻ + 2 H₂O ⇒ H₂ + 2 OH⁻
2 H₂O ⇒ O₂ + 4 H⁺ + 4 e⁻
Oxygen is oxidized since its oxidation number increases from -2 to 0.
Hydrogen is reduced since its oxidation number decreases from +1 to 0.
Arrhenius theory is a theory about acids and bases. It says that acids are those substances that produces hydrogen ions (H+) when in solution and bases are the substances that dissiociates and produces hydroxide ions (OH-). It was introduced by Svante Arrhenius.
Answer:
they become water vapor and after that, they become a type of precipitation
Answer: 6 moles
Take a look at the balanced chemical equation for this synthesis reaction
N 2(g] + 3 H 2(g] → 2 NH 3(g]
Notice that you have a 1:3 mole ratio between nitrogen gas and hydrogen gas. This means that, regardless of how many moles of nitrogen gas you have, the reaction will always consume twice as many moles of hydrogen gas.
So, if you have 2 moles of nitrogen taking part in the reaction, you will need
2 moles N 2 ⋅ 3 moles H 2 /1 mole N 2 = 6 moles H 2
The rate constant of first order reaction at 32. 3 °C is 0.343 /s must be less the 0. 543 at 25°C.
First-order reactions are very commonplace. we have already encountered examples of first-order reactions: the hydrolysis of aspirin and the reaction of t-butyl bromide with water to present t-butanol. every other reaction that famous obvious first-order kinetics is the hydrolysis of the anticancer drug cisplatin.
The value of ok suggests the equilibrium ratio of products to reactants. In an equilibrium combination both reactants and merchandise co-exist. big ok > 1 merchandise are k = 1 neither reactants nor products are desired.
Rate constant K₁ = 0. 543 /s
T₁ = 25°C
Activation energy Eₐ = 75. 9 k j/mol.
T₂ = 32. 3 °C.
K₂ =?
formula;
log K₂/K₁= Eₐ /2.303 R [1/T₁ - 1/T₂]
putting the value in the equation
K₂ = 0.343 /s
Hence, The rate constant of first order reaction at 32. 3 °C is 0.343 /s
The specific rate steady is the proportionality consistent touching on the fee of the reaction to the concentrations of reactants. The fee law and the specific charge consistent for any chemical reaction should be determined experimentally. The cost of the charge steady is temperature established.
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