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:
it is less dense than water
Explanation:
odyssey ware
The answer is A, good luck
An ionic compound is formed between a metal and a non metal. The metal being electropositive can form a cation by transferring the electron to the electronegative non metal that gains the electrons to form an anion. Both the elements try to get a stable octet configuration by the transfer of electrons. The number of electrons lost by metal will be equal to the number of electrons gained by the non metal. Hence, the magnitude of positive charge on the cation will be equal to the magnitude of negative charge on the anion. Therefore, the overall charge on the compound will be 0
So the correct answer is the sum of all charges in the formula for an ionic compound is 0
The answer Fam is B) Models