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: 94.07%
Explanation:
Percentage yield can be calculated by the formula
%yield = Experimental yield/Theoretical yield x100
Experimental yield = 7.93g
Theoretical yield = 8.43
%yield = Experimental yield/Theoretical yield x100
%yield = 7.93/8.43 x 100 = 94.07%
Answer:
p-Nitro acetanilide. 2-Naphthol aniline dye.
Answer:
CnH2n-2
im pretty sure thats the answer
