Explanation:
The structures of both acetone and propanal are shown below:
In the formula of propanal there is -CHO functional group at the end.
In acetone -CO- group is present in the middle that is on the second carbon.
The molecular formula is C3H6O.
Both have same molecular formula but different structural formulas.
It's probably animal if that's what's you're asking.
The moles of O2 are needed to react completely with 1.00 mol of C₂H₂ is 5 mol , 0.23 moles of C₂H₂ are needed to form 0.46 mol of CO₂ .
<h3>What is a Balanced Reaction ?</h3>
A balanced reaction is a reaction in which the number of atoms present in the reactants is equal to the number of atoms in the products.
It is given in the question that
the combustion of Acetylene is given by
2 H―C≡C―H + 5 O₂ → 4 CO₂ + 2 H₂O
Given moles of Acetylene = 1 mol
Moles of oxygen needed = 5 mol
as the mole fraction of Acetylene to Oxygen is 1 :5
The mole of Acetylene needed to form 0.46 mol of CO₂ is ?
mole fraction of CO₂ to Acetylene is 4:2
Therefore 0.23 moles of CO₂ is required.
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Addition of water to an alkyne gives a keto‑enol tautomer product and that is the product changed into 2-pentanone, then the alkyne need to had been 1-pentyne. 2-pentyne might have given a combination of 2- and 3-pentanone.
<h3>
What is the keto-enol means in tautomer?</h3>
They carries a carbonyl bond even as enol implies the presence of a double bond and a hydroxyl group. The keto-enol tautomerization equilibrium is depending on stabilization elements of each the keto tautomer and the enol tautomer.
- The enol that could provide 2-pentanone might had been pent-1- en - 2 -ol. Because an equilibrium favors the ketone so greatly, equilibrium isn't an excellent description.
- If the ketone have been handled with bromine, little response might be visible because the enol content material might be too low.
- If a catalyst have been delivered, NaOH for example, then formation of the enolate of pent-1-en - 2 - ol might shape and react with bromine.
- This might finally provide a bromoform product. Under acidic conditions, the enol might desire formation of the greater substituted enol constant with alkene stability.
