Answer:
The closest shell to the nucleus is called the "1 shell" (also called the "K shell"), followed by the "2 shell" (or "L shell"), then the "3 shell" (or "M shell"), and so on farther and farther from the nucleus.
Answer:
I was traveling on a train where I fell asleep. someone stole my luggage in which I had money and other essentials. when the ticket checker arrived a lady paid my fine. she helped me a lot. when I told her about being robbed she helped me and took me to the police station and I found my bag. I insisted she take the money she paid for my fine but she said that in return you too help someone."I have never found such a kind person ever since.".....
Explanation: I think this is what you are looking for. Hope this helps.
<span>Picture showing seven layers of rocks of different colors labeled A, B, C, D, E, F, and G from top to bottom;
A and B are parallel horizontal layers at the top of the diagram;
C, D, E, F, and G are slanted layers with C closest to the surface and G at the bottom.
</span>
The inference that is most likely correct is that (<span>C) Layer F is younger than Layer D.</span>
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>
Substitution Reactions are those reactions in which one nucleophile replaces another nucleophile present on a substrate. These reactions can take place via two different mechanism i.e SN¹ or SN². In SN¹ substitution reactions the leaving group leaves first forming a carbocation and nucleophile attacks carbocation in the second step. While in SN² reactions the addition of Nucleophile and leaving of leaving group take place simultaneously.
Example:
OH⁻ + CH₃-Br → CH₃-OH + Br⁻
In above reaction,
OH⁻ = Incoming Nucleophile
CH₃-Br = Substrate
CH₃-OH = Product
Br⁻ = Leaving group
Organic reactions are typically slower than ionic reactions because in organic compounds the covalent bonds are first broken, this breaking of bonds is a slower step, while, in ionic compounds no bond breakage is required as it consists of ions, so only bond formation takes place which is a quicker and fast step.
