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:
The peripheral nervous system can be further divided into the autonomic system, which regulates involuntary actions, and the somatic system, which controls voluntary actions.
Explanation:
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Answer:
B. Of
Explanation:
They had good taste of music.
But I think 'in' is the best preposition.
40% solution of glucose is where the solution contains, by weight, 40% glucose and 60% water.
Therefore, if the total weight of the solution is 250 g,
mass of the glucose (C6H12O6) = 250 g * 40% = 100 g
mass of water (H2O) = 250 g * 60% = 150 g
Mass of water can also be calculated by subtracting the weight of glucose from the total weight of the solution:
mass of water = 250g-100g = 150g.