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: ³²P
Explanation:
The radionuclide in question is known as Phosphorus-32. It is an isotope of Phosphorus that is radioactive and has one more neutron than the normal phosphorus does.
Phosphorus does not exist in nature and is created artificially by bombarding the normal stable phosphorus with neutrons. Due to its radioactive nature, it has proven to be useful in the medical industry where it has been used to detect eye tumors as well as in treating some diseases.
You can determine it by paying attention to the unique characteristics that could only be found at heart's tissue, such as :
- looks striated or stripped
- The bundles are breached like tree but connected at both ends
hope this helps