This is an incomplete question, here is a complete question.
Calculate the solubility of each of the following compounds in moles per liter. Ignore any acid-base properties.
CaCO₃, Ksp = 8.7 × 10⁻⁹
Answer : The solubility of CaCO₃ is, 
Explanation :
As we know that CaCO₃ dissociates to give
ion and
ion.
The solubility equilibrium reaction will be:

The expression for solubility constant for this reaction will be,
![K_{sp}=[Ca^{2+}][CO_3^{2-}]](https://tex.z-dn.net/?f=K_%7Bsp%7D%3D%5BCa%5E%7B2%2B%7D%5D%5BCO_3%5E%7B2-%7D%5D)
Let solubility of CaCO₃ be, 's'




Therefore, the solubility of CaCO₃ is, 
Explanation:
speed = distance/time
= 23.7/54 m/s
= 0.44 m/s
speed of a dog running through a field = 0.44 m/s
Answer: The reaction is exothermic reaction as the energy of products is less than the energy of reactants.
Explanation: Exothermic reactions are defined as the reactions in which energy of the product is less than the energy of the reactants. The total energy is released in the form of heat and
for the reaction comes out to be negative.
Labeling of the parts in the diagram:
A represents the activation energy which is the energy required by reactants to cross the energy barrier to get converted to products.
E represents the potential energy of the reactants.
B represents the activated complex.
D represents the potential energy of the products.
C represents the total enthalpy change of the reaction, which comes out to be negative for exothermic reactions.

The complete question is shown in the image attached to this answer.
Answer:
C
Explanation:
Let us quickly remember that the EMF of a cell under non standard conditions in given by the Nernst equation.
This equation states that;
E = E°cell - 0.592/n log Q
Where
E = EMF under non standard conditions
E°cell= standard EMF of the cell
n = number of electrons transferred
Q = reaction quotient
If the reaction quotient is greater than 1 then cell potential is less than the standard cell potential.
The cell that generates the lowest cell potential is the cell depicted in option C because Q has the greatest positive value(Q<1).
We write DE = q+w, where DE is the internal energy change and q and w are heat and work, respectively.
(b)Under what conditions will the quantities q and w be negative numbers?
q is negative when heat flows from the system to the surroundings, and w is negative when the system does work on the surroundings.
As an aside: In applying the first law, do we need to measure the internal energy of a system? Explain.
The absolute internal energy of a system cannot be measured, at least in any practical sense. The internal energy encompasses the kinetic energy of all moving particles in the system, including subatomic particles, as well as the electrostatic potential energies between all these particles. We can measure the change in internal energy (DE) as the result of a chemical or physical change, but we cannot determine the absolute internal energy of either the initial or the final state. The first law allows us to calculate the change in internal energy during a transformation by calculating the heat and work exchanged between the system and its surroundings.