For trans-1-ethyl-4-isopropylcyclohexane, which structures represent the possible boat conformations?
2 answers:
Answer:
C and D on the attached picture.
Explanation:
Hello,
At first, it is important to remember that a cyclohexane beat conformation is a possible shape adopted by this molecule.
In this case, boat conformations are said to be in equilibrium, it means a condition at which the opposing force or influence is balanced with the conformation force. In such way, no changes are noticed as a function of time due to their stability. Thus, the two structure attaining the equilibrium are C and D (attached picture) as result of the distancing between the included radicals.
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Explanation:
According to Le Chatelier's principle, any disturbance caused in an equilibrium reaction will shift the equilibrium in a direction that will oppose the change.
As the given reaction is as follows.
(a) When increase the temperature of the reactants or system then equilibrium will shift in forward direction where there is less temperature. It is possible for an endothermic reaction.
Thus, formation of will increase.
- (b) When we decrease the volume (at constant temperature) of given reaction mixture then it implies that there will be increase in pressure of the system. So, equilibrium will shift in a direction where there will be decrease in composition of gaseous phase. That is, in the backward direction reaction will shift.
Hence, formation of will decrease with decrease in volume.
- When we increase the mount of
then equilibrium will shift in the direction of decrease in concentration that is, in the forward direction.
Thus, we can conclude that formation of will increase then.
The ions in the unknown salt are:
and
The chemical formula of the salt is determined as shown in the picture.
The chemical formula of the salt is .
