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AlekseyPX
3 years ago
5

Consider the following system at equilibrium:

Chemistry
1 answer:
alexgriva [62]3 years ago
6 0

Answer:

A - Increase (R), Decrease (P), Decrease(q), Triple both (Q) and (R)

B - Increase(P), Increase(q), Decrease (R)

C - Triple (P) and reduce (q) to one third

Explanation:

<em>According to Le Chatelier principle, when a system is in equilibrium and one of the constraints that affect the rate of reaction is applied, the equilibrium will shift so as to annul the effects of the constraint.</em>

P and Q are reactants, an increase in either or both without an equally measurable increase in R (a product) will shift the equilibrium to the right. Also, any decrease in R without a corresponding decrease in either or both of P and Q will shift the equilibrium to the right. Hence, Increase(P), Increase(q), and Decrease (R) will shift the equilibrium to the right.

In the same vein, any increase in R without a corresponding increase in P and Q will shift the equilibrium to the left. The same goes for any decrease in either or both of P and Q without a counter-decrease in R will shift the equilibrium to the left. Hence, Increase (R), Decrease (P), Decrease(q), and Triple both (Q) and (R) will shift the equilibrium to the left.

Any increase or decrease in P with a commensurable decrease or increase in Q (or vice versa) with R remaining constant will create no shift in the equilibrium. Hence, Triple (P) and reduce (q) to one third will create no shift in the equilibrium.

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See explanation and image attached

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Here attached are resonance forms of pyrrole and pyridine. The images were obtained from quora and researchgate respectively.

Now, we can see that in the resonance forms of pyrrole, the nitrogen atom in the heterocycle has a formal charge of +1. However, in the six membered pyridine hetrocycle, the nitrogen atom may have a formal charge of -1 or +1 as shown in the canonical structures attached. The structures in which nitrogen has a +1 formal charge in pyridine are comparable to structures obtained from pyrrole. These structures have less contribution to the structure of pyridine.

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