Answer and explanation:
cyclopentadiene is more acidic than cyclopentane
hydrocarbon compound are weak acid in nature
This relative acidity is explained by the stability of
cyclopentadienyl anion which is aromatic in nature
(check the attached image file 1)
To answer this question we must look at the stability of the anions that are formed when the compound lose proton.
All the electron in the cyclopentyl anion are localized.
In contrast, the aromatic cyclopentadienyl anion is a stable carbanion as a result of its aromaticity therefore making its conjugate acid a very strong acid compare to other compounds with hydrogen attached to sp³ carbons
In physics, a force is any interaction that, when unopposed, will change the motion of an object. A force can cause an object with mass to change its velocity to accelerate. Force can also be described intuitively as a push or a pull. A force has both magnitude and direction, making it a vector quantity.
The action is interaction
When we can get the Kinetic energy from this formula KE= 1/2 M V^2and we can get the potential energy from this formula PE = M g H
we can set that the kinetic energy at the bottom of the fall equals the potential energy at the top so, KE = PE
1/2 MV^2 = M g H
1/2 V^2 = g H
when V is the velocity, g is an acceleration of gravitational force (9.8 m^2/s) and H is the height of the fall (8 m).
∴ v^2 = 2 * 9.8 * 8 = 156.8
∴ v= √156.8 = 12.5 m/s
