Predict the product one would expect from the following reaction. ### Explanation of Forces on a Seesaw**Introduction:**A seesaw is a classic example of rotational dynamics and equilibrium in physics. By examining the forces acting on a seesaw, we can learn about torque, balance, and how rotational forces affect motion.**Diagram Description:**1. **Fulcrum (F):** - Located at the center, it is the pivot point of the seesaw, allowing it to rotate. It is marked with a triangle and labeled "F". 2. **Hierarchic Arrangement:** - The seesaw board is balanced over the fulcrum. - Seats are positioned on either end for individuals to apply forces.3. **Forces Applied:** - Two key forces are applied on this system: - \( F_1 \), acting downward on the left side of the seesaw, with the magnitude of 90 N. - \( F_2 \), acting downward on the right side of the seesaw, with the magnitude of 60 N.4. **Distance from Fulcrum:** - \( d_1 \) refers to the distance from the fulcrum to the point where \( F_1 \) is applied, marked as 9 m. - \( d_2 \) refers to the distance from the fulcrum to the point where \( F_2 \) is applied, marked as 3 m.5. **Torque and Equilibrium:** - Torque (\(\tau\)) is calculated by the product of force and the distance from the fulcrum (\(\tau = F \times d\)). - For equilibrium, the torques on both sides of the fulcrum must be equal. - The equation for equilibrium is: \( F_1 \times d_1 = F_2 \times d_2 \).**Conclusion:**This diagram serves as a simple representation of balancing forces in a rotational system. Understanding how torque works helps in solving problems related to equilibrium and dynamics of bodies in rotational motion.This image can be used to illustrate principles of physics for educational purposes, demonstrating how different forces affect movement and balance on a seesaw.

The given reaction is the cleavage of ether in the acid medium like HCl and HBr. The reaction is similar to that of a nucleophilic substitution reaction.The major products formed in the reaction are phenol and n-propyl bromide. There is also a possibility of the formation of chlorobenzene and n-propyl alcohol, but the major product is phenol due to the formation of resonance stabilized phenoxide ion.