One of the wavelengths of light emitted by hydrogen atoms is 6.56 x 10-7 m. Calculate the Energy.
1 answer:
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Answer:
Explanation:
We want to convert from moles to grams, so we must use the molar mass.
<h3>1. Molar Mass</h3>The molar mass is the mass of 1 mole of a substance. It is the same as the atomic masses on the Periodic Table, but the units are grams per mole (g/mol) instead of atomic mass units (amu).
We are given the compound PI₃ or phosphorus triiodide. Look up the molar masses of the individual elements.
- Phosphorus (P): 30.973762 g/mol
- Iodine (I): 126.9045 g/mol
Note that there is a subscript of 3 after the I in the formula. This means there are 3 moles of iodine in 1 mole of the compound PI₃. We should multiply iodine's molar mass by 3, then add phosphorus's molar mass.
- I₃: 126.9045 * 3=380.7135 g/mol
- PI₃: 30.973762 + 380.7135 = 411.687262 g/mol
Use the molar mass as a ratio.
We want to convert 3.14 moles to grams, so we multiply by that value.
The units of moles of PI₃ cancel.
The original measurement of moles has 3 significant figures, so our answer must have the same. For the number we calculated, that is the tens place.
- 1292.698
The 2 in the ones place tells us to leave the 9.
3.14 moles of phosphorous triiodide is approximately equal to <u>1290 grams of phosphorus triodide.</u>
Answer:
See explanation below
Explanation:
The question is incomplete. However in picture 1, you have the starting materials and the structure of the product, which you miss in this part.
Now, in picture 2, you have the starting reactant and the product, and the mechanism that is taking place here.
First, all what we have here is an acid base reaction. In the first step, we are using the acid medium to convert the reactant into an alcohol. The bromine there, is not leaving the molecule yet, because it's neccesary for the next step. The starting reactant is an alkene, in that way, we can convert the reactant in the first step into a secondary alcohol. In other words, the first reaction is a alkene hydration.
In the second step, we use a strong base. You may say this is a strong nucleophile and will do a Sn2 reaction to form another alcohol there, but it's not the case, because, before any kind of reaction happens, the priority here is always the acid base, so the base will react with the acidic hydrogen. In this case, it will substract an hydrogen from the OH. When this happens, the lone pair will do an auto condensation here, and attacks the bromine in the molecule. In this way, the molecule will become a cyclomolecule, and that way it form the final product.
See picture 2, for mechanism
