Answer:
The concentration of cyclopropane after 22.0 hour is 0.0457 M.
Explanation:
Conversion of cyclopropane into propene follows first order kinetics.
The integrated rate of first order kinetic is given by :
![[A]=[A_o]\times e^{-kt}](https://tex.z-dn.net/?f=%5BA%5D%3D%5BA_o%5D%5Ctimes%20e%5E%7B-kt%7D)
![[A_o]](https://tex.z-dn.net/?f=%5BA_o%5D)
= Initial concentration of reactant
![[A]](https://tex.z-dn.net/?f=%5BA%5D)
= final concentration of reactant after time t
k = rate constant of the reaction
We have :
Rate constant of the reaction = k = 
![[A_o]=0.150 M](https://tex.z-dn.net/?f=%5BA_o%5D%3D0.150%20M)
t = 22.0 hour
[A] =?
![[A]=0.150 M\times e^{-5.4\times 10^{-2} hour^{-1}\times 22.hour}](https://tex.z-dn.net/?f=%5BA%5D%3D0.150%20M%5Ctimes%20e%5E%7B-5.4%5Ctimes%2010%5E%7B-2%7D%20hour%5E%7B-1%7D%5Ctimes%2022.hour%7D)
![[A]=0.0457 M](https://tex.z-dn.net/?f=%5BA%5D%3D0.0457%20M)
The concentration of cyclopropane after 22.0 hour is 0.0457 M.
A scientist would most likely need to update her model when it no longer supports the latest results.
Answer:
C2H3Br + O2 → CO2 + H2O + HBr
Explanation:
The term balancing of chemical reaction equation has a unique meaning in chemistry. What it actually means is to ensure that the number of atoms of each element on the left hand side of reaction equation becomes equal to the number of atoms of the same element on the right hand side of the reaction equation.
When we look at the equation; C2H3Br + O2 → CO2 + H2O + HBr, the number of atoms of each element on the left and right hand sides of the given equation are not the same hence the equation is unbalanced.
If we look at the equation; 2C2H3Br + 5O2 → 4CO2 + 2H2O + 2HBr, the number of atoms of each element on both sides of the reaction equation are now equal, thus the later equation is the balanced version of the former.
They will attract each other when brought close but when they touch the glass rod will become a negative charge and will repel each other
Answer:
Axial position
Explanation:
In the reduction of 4-tert-butylcyclohexanone with sodium borohydride, the major product has the tert-butyl group in the equatorial position and the alcohol in the axial position.
The reason for this is that, axial bonds are parallel to each other. If substituents are larger than hydrogen, they experience a greater steric crowding in axial compared to the equatorial position. Therefore, many substituted cyclohexane compounds prefer a conformation in which the larger substituents are in equatorial position.
