Answer:
a) The equilibrium will shift in the right direction.
b) The new equilibrium concentrations after reestablishment of the equilibrium :
![[SbCl_5]=(0.370-x) M=(0.370-0.0233) M=0.3467 M](https://tex.z-dn.net/?f=%5BSbCl_5%5D%3D%280.370-x%29%20M%3D%280.370-0.0233%29%20M%3D0.3467%20M)
![[SbCl_3]=(6.98\times 10^{-2}+x) M=(6.98\times 10^{-2}+0.0233) M=0.0931 M](https://tex.z-dn.net/?f=%5BSbCl_3%5D%3D%286.98%5Ctimes%2010%5E%7B-2%7D%2Bx%29%20M%3D%286.98%5Ctimes%2010%5E%7B-2%7D%2B0.0233%29%20M%3D0.0931%20M)
![[Cl_2]=(6.98\times 10^{-2}+x) M=(6.98\times 10^{-2}+0.0233) M=0.0931 M](https://tex.z-dn.net/?f=%5BCl_2%5D%3D%286.98%5Ctimes%2010%5E%7B-2%7D%2Bx%29%20M%3D%286.98%5Ctimes%2010%5E%7B-2%7D%2B0.0233%29%20M%3D0.0931%20M)
Explanation:
a) Any change in the equilibrium is studied on the basis of Le-Chatelier's principle.
This principle states that if there is any change in the variables of the reaction, the equilibrium will shift in the direction to minimize the effect.
On increase in amount of reactant
If the reactant is increased, according to the Le-Chatlier's principle, the equilibrium will shift in the direction where more product formation is taking place. As the number of moles of 
is increasing .So, the equilibrium will shift in the right direction.
b)
Concentration of = 0.195 M
Concentration of 
= 
Concentration of 
=
On adding more 
to 0.370 M at equilibrium :
Initially
0.370 M 
At equilibrium:
(0.370-x)M 
The equilibrium constant of the reaction = 
The equilibrium expression is given as:
![K_c=\frac{[SbCl_3][Cl_2]}{[SbCl_5]}](https://tex.z-dn.net/?f=K_c%3D%5Cfrac%7B%5BSbCl_3%5D%5BCl_2%5D%7D%7B%5BSbCl_5%5D%7D)
On solving for x:
x = 0.0233 M
The new equilibrium concentrations after reestablishment of the equilibrium :
D = m/ V
8.9 = 3 / V
V = 3 / 8.9
V = 0.3 cm³
Answer A
hope this helps!
<span>What is the atomic number of the first element to start filling an "f" sub-level?
the answer is 58.
I hope this helps :)</span>
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Although phlorizin inhibition of Na+-glucose cotransport occurs within a few seconds, 3H-phlorizin binding to the sodium-coupled glucose transport protein(s) requires several minutes to reach equilibrium (the fast-acting slow-binding paradigm). Using kinetic models of arbitrary dimension that can be reduced to a two-state diagram according to Cha’s formalism, we show that three basic mechanisms of inhibitor binding can be identified whereby the inhibitor binding step either (A) represents, (B) precedes, or (C) follows the rate-limiting step in a binding reaction. We demonstrate that each of mechanisms A–C is associated with a set of unique kinetic properties, and that the time scale over which one may expect to observe mechanism C is conditioned by the turnover number of the catalytic cycle. In contrast, mechanisms A and B may be relevant to either fast-acting or slow-binding inhibitors.
Explanation:
Answer:
I feel as though you are missing information to this question.
Explanation:
elements on the periodic table, today, are arranged based on physical properties, such as valence electrons, atomic mass, etc.
