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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.
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Answer:
D) It has a different unit than atomic mass.
Answer : The molarity of
in the solution is 1.5 M.
Explanation : Given,
Moles of
= 3.0 mol
Volume of solution = 2.00 L
Molarity : It is defined as the number of moles of solute present in one liter of volume of solution.
Formula used :
![\text{Molarity}=\frac{\text{Moles of }KF}{\text{Volume of solution (in L)}}](https://tex.z-dn.net/?f=%5Ctext%7BMolarity%7D%3D%5Cfrac%7B%5Ctext%7BMoles%20of%20%7DKF%7D%7B%5Ctext%7BVolume%20of%20solution%20%28in%20L%29%7D%7D)
Now put all the given values in this formula, we get:
![\text{Molarity}=\frac{3.0mol}{2.00L}=1.5mole/L=1.5M](https://tex.z-dn.net/?f=%5Ctext%7BMolarity%7D%3D%5Cfrac%7B3.0mol%7D%7B2.00L%7D%3D1.5mole%2FL%3D1.5M)
Therefore, the molarity of
in the solution is 1.5 M.