Answer:
Mn^2+(aq) + 4H2O(l) + 5[VO2]^+(aq) + 10H^+(aq) ---------->MnO4^-(aq) + 8H^+(aq) + 5[VO]^2+(aq) + 5H2O(l)
Explanation:
Oxidation half equation:
Mn^2+(aq) + 4H2O(l) ------------> MnO4^-(aq) + 8H^+(aq) + 5e
Reduction half equation:
5[VO2]^+(aq) + 10H^+(aq) + 5e --------> 5[VO]^2+(aq) + 5H2O(l)
Overall redox reaction equation:
Mn^2+(aq) + 4H2O(l) + 5[VO2]^+(aq) + 10H^+(aq) ---------->MnO4^-(aq) + 8H^+(aq) + 5[VO]^2+(aq) + 5H2O(l)
False the opposite should happen!
Answer:
See explanation and picture below
Explanation:
First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.
In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.
In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.
Answer: Potassium perchlorate
Explanation:
Answer:
pH = 4.17
Explanation:
According to the molar concentration you stated, pH of the solution is: 4.17
Remember that pH = - log [H⁺]
and [H⁺] = 10^-pH
When:
pH > 7 → Basic solution
pH = 7 → Neutral solution
pH < 7 → Acid solution