Complete the mechanism for the keto-enol tautomerization below using bonds, charges, nonbonding electron pairs, and curved arrow
s (forward reaction only). Use the existing electrons and charges as guides to completing the mechanism of the tautomerization. Do not remove any pre-drawn bonds/lone pairs.
1 answer:
Answer:
Check the explanation
Explanation:
In the field of organic chemistry, keto–enol tautomerism refers to equilibrium of chemical substance that is among a keto form (an aldehyde or a ketone) and an enol (an alcohol). The enol and the keto forms are believed to be tautomers of each other. The keto form preponderate at equilibrium for a large amount of ketones.
Kindly check the diagram image below to see the solution to the above question:
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Answer: V=67.2 L
Explanation:
For this problem we will need to use the Ideal Gas Law.
Ideal Gas Law: PV=nRT
P=1.00 atm (STP)
V=?
n=3.00 mol
R=0.08206Latm/Kmol
T=273.15 K (STP)
To find V, we would manipulate the equation to V=nRT/P
With significan figures, our answer is V=67.2 L.