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:
0.05
moles
Explanation:
In a mole of any substance, there exist
6.02⋅1023
units of that substance.
So here, we got:
3.01⋅1022Mg atoms⋅1mol6.02⋅1023M gatoms=0.05mol
Answer:
The pineal, hypothalamus, and pituitary are located in the BRAIN
The thyroid, parathyroid, and thymus are located in the
THROAT
The adrenals, pancreas, testes, and ovaries are located in the NEAR THE KIDNEY
Explanation:
The pineal, hypothalamus, and pituitary are located in the BRAIN
The thyroid, parathyroid, and thymus are located in the
THROAT
The adrenals, pancreas, testes, and ovaries are located in the NEAR THE KIDNEY
Answer:
ALA.American Institute of Architects
SAG.Screen Actor Guild
AFP.Association For Finance Professional
AMA.American Medical Association
A) Deer
D) Grass
Hope that helps you out (: