Alkene on
Hydration yield
Alcohols. When
Asymmetric Alkenes are treated with water in the presence of acid they follow
Markovnikoff rule, and the Hydrogen of incoming reagent goes to that carbon which contain more number of Hydrogen atoms. The reverse (
Anti-Markovnikoff) is done by carrying out Hydroboration reaction.In this case the Hydrogen atom of incoming reagent goes to that carbon which contains less number of Hydrogen atoms. In this reaction both -H and -OH adds in
syn fashion. The Hydroboration reaction of
Chloestrol is shown below,
Answer:
Option B
Explanation:
As Brønsted-Lowry theory states, acids are the ones that can donate protons.
When a proton is donated, it is released to become medium more acidic.
HCl is a strong acid.
HCl (l) + H₂O (l) → H₃O⁺ (aq) + Cl⁻(aq)
These always reffers to strong acid where the dissociation is 100% completed.
In a weak acid, dissociation is not 100% complete, that's why we have an equilibrium.
HA (l) + H₂O (l) ⇄ H₃O⁺ (aq) + A⁻(aq) Ka
An ambient pressure of 1 atm
I think it’s 2.45, not 100% sure