Answer:
C.5
Explanation:
A number of electrons present in valence shell of penultimate Shell represents the group of elements.
For s block elements: no.of group=number of valence shell electron.
p block elements: no. of group= 2 + 10 + number of valence electrons.
d block elements: no. of group= number(n-1)d electrons + number of electrons in nth shell.
Here, the differential electron is in p orbital hence, it belongs to p block
No. of group= 2+ 10 + 3=15 i.e 15th group or VA group.
The answer is going to be Rubidium. hope that helped
Answer:
Final pH of the solution: 2.79.
Explanation:
What's in the solution after mixing?
,
where
is the concentration of the solute,
is the number of moles of the solute, and
is the volume of the solution.
.
Acetic (ethanoic) acid:
.
.
Hydrochloric acid HCl:
.
.
HCl is a strong acid. It will completely dissociate in water to produce H⁺. The H⁺ concentration in the solution before acetic acid dissociates shall also be
.
The Ka value of acetic acid is considerably small. Acetic acid is a weak acid and will dissociate only partially when dissolved. Construct a RICE table to predict the portion of acetic acid that will dissociate. Let the change in acetic acid concentration be
.
.
.
.
Rewrite as a quadratic equation and solve for
:

.
The pH of a solution depends on its H⁺ concentration.
At equilibrium
.
.
We are going to use this formula:
E° = 0.0592/ n * ㏒K
when E° is the standard state cell potential
and n is number of moles of electrons transferred in the balanced equation
for the reaction of the cell.
Sr(s) + Mg2+ (aq) ↔ Sr2+(aq) + Mg(s)
we can get it by using the given balanced equation, we here have 2 electrons
transferred so, n = 2
and K the equilibrium constant = 3.69 x 10^17
so, by substitution:
∴ E° = 0.0592 / 2 * ㏒ (3.69 x 10^17)
= 0.52 V
<h2>Competitive inhibitors.</h2>
Explanation:
▪ Transition state analogs can be used as inhibitors in enzyme-catalyzed reactions which are done by blocking the active site of the enzyme.
▪ A transition state analog is somewhat the same as that of the transition state.
▪These are better inhibitors than the substrate analogs in competitive inhibition, the reason is that they bind tighter to the enzyme rather than the substrate.
▪ Thus, they are classified as competitive inhibitors.