Answer:
-1 Coulomb meter = -2.997 × 10²⁹ Debye
Explanation:
Given:
Coulomb meter = -1 CM
Find:
In debye
Computation:
We know that,
1 Coulomb meter = 299,792,458,178,090,000,000,000,000,000 Debye
So,
-1 Coulomb meter = -299,792,458,178,090,000,000,000,000,000 Debye
-1 Coulomb meter = -2.997 × 10²⁹ Debye
Answer:
Nuclear fission
Explanation:
All nuclear reactors in operation are based on the principle of nuclear fission of Uranium nuclide to produce energy. These is produced is being controlled and is used in heating water to steam. The steam is then harnessed to drive or power steam turbines which is used for the generation of electricity.
Answer:
The combined mass of all the protons and electrons is 24.305.
Explanation:
From the information given about the atom, we can see that the relative atom mass of the element is 24.305.
The relative atomic mass of an atom is the combined mass of all its isotope in proportion of their geonormal abundances. On the periodic table, this mass deals with the amount of protons and neutrons present in a given atom.
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.
It’s C I think and I’m not sure