Answer:
See explanation
Explanation:
The question is incomplete because the image of the alcohol is missing. However, I will try give you a general picture of the reaction known as hydroboration of alkenes.
This reaction occurs in two steps. In the first step, -BH2 and H add to the same face of the double bond (syn addition).
In the second step, alkaline hydrogen peroxide is added and the alcohol is formed.
Note that the BH2 and H adds to the two atoms of the double bond. The final product of the reaction appears as if water was added to the original alkene following an anti-Markovnikov mechanism.
Steric hindrance is known to play a major role in this reaction as good yield of the anti-Markovnikov like product is obtained with alkenes having one of the carbon atoms of the double bond significantly hindered.
Answer:
its easy ask to chrome or search in yt ;)
Answer:
I think mixture
Explanation:
Mixture because it is a mixture of water and carbon
Answer:
56.9 mmoles of acetate are required in this buffer
Explanation:
To solve this, we can think in the Henderson Hasselbach equation:
pH = pKa + log ([CH₃COO⁻] / [CH₃COOH])
To make the buffer we know:
CH₃COOH + H₂O ⇄ CH₃COO⁻ + H₃O⁺ Ka
We know that Ka from acetic acid is: 1.8×10⁻⁵
pKa = - log Ka
pKa = 4.74
We replace data:
5.5 = 4.74 + log ([acetate] / 10 mmol)
5.5 - 4.74 = log ([acetate] / 10 mmol)
0.755 = log ([acetate] / 10 mmol)
10⁰'⁷⁵⁵ = ([acetate] / 10 mmol)
5.69 = ([acetate] / 10 mmol)
5.69 . 10 = [acetate] → 56.9 mmoles
