Answer:The IUPAC name of compound would be Hex-3-yn-ol
Explanation:
When butyne is treated with LDA it leads to generation of carbanion on the terminal alkyne.
As LDA is disopropyl amide which happens to be quite a good base and hence it is sufficiently basic to abstract the acidic proton on the terminal alkyne.
So this proton abstraction leads to generation of a carbanion which can now acts as a nucleophile in step 2.
In step 2 the generated carbanion attacks the strained epoxide ring to open the strained epoxide ring .The product of step 2 leads to generation of hex-3-yn-1-olate
Further on treating the product formed in step 2 with the dilute acid it leads to the formation of alcohol as the negative charge on oxygen can now be neutralised.
Kindly refer the mechanism for structure of compounds.
To work this out you do 400÷20=20
Answer:
3.1 kg
Explanation:
Step 1: Write the balanced combustion equation
C₈H₁₈ + 12.5 O₂ ⇒ 8 CO₂ + 9 H₂O
Step 2: Calculate the moles corresponding to 1.0 kg of C₈H₁₈.
The molar mass of C₈H₁₈ is 114.23 g/mol.
1.0 × 10³ g × 1 mol/114.23 g = 8.8 mol
Step 3: Calculate the moles of CO₂ produced from 8.8 moles of C₈H₁₈
The molar ratio of C₈H₁₈ to CO₂ is 1:8. The moles of CO₂ produced are 8/1 × 8.8 mol = 70 mol.
Step 4: Calculate the mass corresponding to 70 moles of CO₂
The molar mass of CO₂ is 44.01 g/mol.
70 mol × 44.01 g/mol = 3.1 × 10³ g = 3.1 kg
The answer should be C makes very snesen