Answer:
He took a deep breath and splashed some water on his face.
Explanation:
I took the test on Edmentum.
<span>0.0165 m
The balanced equation for the reaction is
AgNO3 + MgCl2 ==> AgCl + Mg(NO3)2
So it's obvious that for each Mg ion, you'll get 1 AgCl molecule as a product. Now calculate the molar mass of AgCl, starting with looking up the atomic weights.
Atomic weight silver = 107.8682
Atomic weight chlorine = 35.453
Molar mass AgCl = 107.8682 + 35.453 = 143.3212 g/mol
Now how many moles were produced?
0.1183 g / 143.3212 g/mol = 0.000825419 mol
So we had 0.000825419 moles of MgCl2 in the sample of 50.0 ml. Since concentration is defined as moles per liter, do the division.
0.000825419 / 0.0500 = 0.016508374 mol/L = 0.016508374 m
Rounding to 3 significant figures gives 0.0165 m</span>
A free-radical substitution reaction is likely to be responsible for the observations. The reaction mechanism of a reaction like this can be grouped into three phases:
- Initiation; the "light" on the mixture deliver sufficient amount of energy such that the halogen molecules undergo homologous fission. It typically takes ultraviolet radiation to initiate fissions of the bonds.
- Propagation; free radicals react with molecules to produce new free radicals and molecules.
- Termination; two free radicals combine and form covalent bonds to produce stable molecules. Note that it is possible for two carbon-containing free-radicals to combine, leading to the production of trace amounts of long carbon chains in the product.
Initiation
where the big black dot indicates unpaired electrons attached to the atom.
Propagation
Termination
The hydrocarbon is used in excess.
<h3><u>Explanation</u>:</h3>
The bromination of an arene is not simple as bromination of an alkane. This is because the carbocation or free radicle formation in benzene is a very energy consuming process. This is why a lewis base like aluminium bromide or ferric bromide is used. The ferric bromide takes in the bromine radicle and forms the brominium cation which helps in the formation of electrophile. Now this electrophile brominium cation attacks the benzene ring and forms a temporary sp3 hybrid carbon intermediate. Then the hydrogen is taken by the FeBr4- forming HBr and regenerating the FeBr3 as well as Aromaticity of the arene species at the same time. Here hydrocarbon is used in excess just to prevent the chances of multiple substitution in the same arene molecule.