Answer:
See explanation below
Explanation:
Ok, the first picture is your exercise. We have one type of reaction to form the 3-methyl-3-hexanol.
Now, according to the question, you want another form to get the 3-methyl-3-hexanol. In this case, the easiest way to do this, is using a ketone with the 6 carbons, and the grignard reagent to use should have the methyl group. Now, in which carbon should the carbonile group be? well, as the final product has the OH group in carbon 3, then the reaction is taking place there. So the reactants would be the hexan- 3 - one and the methyl magnesium bromide.
The second picture, you'll see the reactants and final product.
Hope this helps
second compound
Let molar mass of x is = X
Let molar mass of y is = Y
Moles of x in second compound = Mass / molar mass = 7 / X
Moles of y in second compound = Mass / molar mass = 4.5 / Y
For second compound
7 / X : 4.5/ Y = 1:1
Therefore
X / Y = 7/4.5
Y / X = 4.5/ 7
The mass of x in first compound = 14g
moles of x in first compound = 14/X
Mass of y in first compound = 3
moles of y in first compound = 3 / Y
14 / X : 3/ Y = 14Y / 3X = 14 X 4.5 / 3 X 7 = 3 :1
Thus molar ratio in first compound = moles of x / Moles of y = 3:2
Formula = x3y
We know this because of the discovery of fossils and bones. We can find out roughly when they existed because of carbon dating.
Option c. dendrochronology
tree rings or dendrochronology they allow to use it in calibration for carbon-14 on temporal placements of fragments of wood (from long dead trees).
Example Bristle cone pines (1957) 4723 years old
