Find if the example is correct or not and explain using CER please. Will give 5/5
1 answer:
The Lewis structure the student drew is incorrect. The total number of electrons in bonds and lone pairs is equal to the total number of valence electrons available, then a valid Lewis structure is produced.
The correct structure is the following:
The structure that was drawn by the student was incorrect because the total number of electrons around Oxygen were incorrect, there were 6 instead of 8, which was against the octet rule. The correct structure should have 8 electrons around each atom.
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Answer:
- <u>First choice: 0.042</u>
Explanation:
Given decomposition reaction:
- 1PCl₅ (g) ⇄ 1PCl₃ + 1Cl₂(g)
Equilibrium constant:
Stoichiometric coefficients and powers equal to 1 are not usually shown as they are understood, but I included them in order to shwow you how they intervene in the equilibrium expressions: each concentration is raised to a power equal to the respective stoichiometric coefficient in the equilibrium equation.
So, your calculations are:
Answer:
See explanation below
Explanation:
The question is incomplete. However in picture 1, you have the starting materials and the structure of the product, which you miss in this part.
Now, in picture 2, you have the starting reactant and the product, and the mechanism that is taking place here.
First, all what we have here is an acid base reaction. In the first step, we are using the acid medium to convert the reactant into an alcohol. The bromine there, is not leaving the molecule yet, because it's neccesary for the next step. The starting reactant is an alkene, in that way, we can convert the reactant in the first step into a secondary alcohol. In other words, the first reaction is a alkene hydration.
In the second step, we use a strong base. You may say this is a strong nucleophile and will do a Sn2 reaction to form another alcohol there, but it's not the case, because, before any kind of reaction happens, the priority here is always the acid base, so the base will react with the acidic hydrogen. In this case, it will substract an hydrogen from the OH. When this happens, the lone pair will do an auto condensation here, and attacks the bromine in the molecule. In this way, the molecule will become a cyclomolecule, and that way it form the final product.
See picture 2, for mechanism
