NH₃:
N = 8*10²²
NA = 6.02*10²³
n = N/NA = 8*10²²/6.02*10²³ ≈ 1.33*10⁻¹=0.133mol
O₂:
N=7*10²²
NA = 6.02*10²³
n = N/NA = 7*10²²/6.02*10²³ = 1.16*10⁻¹=0.116mol
4NH₃ <span>+ 3O</span>₂ ⇒<span> 2N</span>₂<span> + 6H</span>₂<span>O
</span>4mol : 3mol : 2mol
0.133mol : 0.116mol : 0,0665mol
limiting reactant
N₂:
n = 0.0665mol
M = 28g/mol
m = n*M = 0.0665mol*28g/mol = <u>1,862g</u>
The solution would be like this for this specific problem:
Given:
pH of a 0.55 M hypobromous
acid (HBrO) at 25.0 °C = 4.48
[H+] = 10^-4.48 = 3.31 x
10^-5 M = [BrO-] <span>
Ka = (3.31 x 10^-5)^2 / 0.55 = 2 x 10^-9</span>
To add, Hypobromous Acid does not require acid
adjustment, which is necessary for chlorine-based product and is stable and
effective in pH ranges of 5-9.<span>
</span>Hypobromous Acid combines with organic
compounds to form a bromamine. Chlorine also combines with the same organic
compounds to form a chloramine. <span>It is also
one of the least expensive intervention antimicrobial compounds available.</span>
<span>Name of type of mechanism </span>initiation step<span> first </span>propagation step<span> second </span>propagation step<span>(ii) </span>write<span> an overall </span>equation<span> for the </span>formation of dichloromethane<span> from ... Best Answer: i) This is a </span>free-radical<span> substitution mechanism.</span>
In order to synthesize a complex organic molecule, the
chemist should at least illustrate or imagine the bonds that are in need to be
cut down or to separate in order to obtain the compound that can be easily
changed.
