Answer:
See attachment.
Explanation:
Mono-substituted cyclohexanes are more stable with their substituents in an equatorial position. However, with poly-substituted cyclohexanes, the situation is more complex since the steric effects of all substituents have to be taken into account. In this case, you can see that <u>the interconversion is shifted towards the conformation in the bottom because there is less tension between the substituents</u>.
Answer:
The correct answer is : 'the concatenation of NO will increase'.
Explanation:
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.
If the temperature is increased, so according to the Le-Chatlier's principle , the equilibrium will shift in the direction where increase in temperature occurs.
As, this is an endothermic reaction, increasing temperature will add more heat to the system which move equilibrium in the forward reaction with decrease in temperature. Hence, the equilibrium will shift in the right direction.
So, the concatenation of NO will increase.