Answer: Thermal Equilibrium
Explanation:
Answer:
Concentration of hydrogen ion, ![[H^+]=5.0118*10^{-6} M](https://tex.z-dn.net/?f=%5BH%5E%2B%5D%3D5.0118%2A10%5E%7B-6%7D%20M)
Explanation:
pH is defined as the negative logarithm of hydrogen ion's concentration.
The lower the value of pH, the higher the acidic the solution is.
The formula for pH can be written as:
![pH=-log[H^+]](https://tex.z-dn.net/?f=pH%3D-log%5BH%5E%2B%5D)
Given,
pH of the saliva of Marco = 5.3
To calculate: Hydrogen ion concentration in the saliva
Thus, applying in the formula as:
![pH=-log[H^+]](https://tex.z-dn.net/?f=pH%3D-log%5BH%5E%2B%5D)
![5.3=-log[H^+]](https://tex.z-dn.net/?f=5.3%3D-log%5BH%5E%2B%5D)
So,
![log[H^+]=-5.3](https://tex.z-dn.net/?f=log%5BH%5E%2B%5D%3D-5.3)
![[H^+]=10^{(-5.3)}](https://tex.z-dn.net/?f=%5BH%5E%2B%5D%3D10%5E%7B%28-5.3%29%7D)
![[H^+]=5.0118*10^{-6} M](https://tex.z-dn.net/?f=%5BH%5E%2B%5D%3D5.0118%2A10%5E%7B-6%7D%20M)
Answer:
See explanation
Explanation:
The mechanism of this reaction including intermediates are shown in the image attached to this answer.
The reaction of HBr with 3-bromocyclohexene yields trans-1,2-dibromocyclohexane as the sole product because; the proton first attacks the 3-bromocyclohexene and a brominium ion is formed. This brominium ion is a cyclic intermediate as shown in the image attached.
Attack of a bromine ion afterwards must lead to the formation of trans-1,2-dibromocyclohexane as shown.
Answer:
A strong base is something like sodium hydroxide or potassium hydroxide which is fully ionic. You can think of the compound as being 100% split up into metal ions and hydroxide ions in solution.
Explanation:
Answer:
Epoxides, also called oxiranes, have a three-membered ring structure with one oxygen and two carbon atoms.
Epoxides can be formed from alkenes by reaction with peroxy acids (MCPBA for example).
Epoxides can be formed from halohydrin molecules by reaction with a base, which causes an intramolecular Williamson ether synthesis.
Explanation:
Epoxide, cyclic ether with a three-membered ring. The basic structure of an epoxide contains an oxygen atom attached to two adjacent carbon atoms of a hydrocarbon. The strain of the three-membered ring makes an epoxide much more reactive than a typical acyclic ether.