Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
It's the eye because it's the organ of sight
Li is in group 1 so it has same number of valence electrons as hydrogen.
hope it helps.
FeBr₃ ⇒ limiting reactant
mol NaBr = 1.428
<h3>Further explanation</h3>
Reaction
2FeBr₃ + 3Na₂S → Fe₂S₃ + 6NaBr
Limiting reactant⇒ smaller ratio (mol divide by coefficient reaction)
211 g of Iron (III) bromide(MW=295,56 g/mol), so mol FeBr₃ :
186 g of Sodium sulfide(MW=78,0452 g/mol), so mol Na₂S :
Coefficient ratio from the equation FeBr₃ : Na₂S = 2 : 3, so mol ratio :
So FeBr₃ as a limiting reactant(smaller ratio)
mol NaBr based on limiting reactant (FeBr₃) :
Answer:
384.2 K
Explanation:
First we convert 27 °C to K:
- 27 °C + 273.16 = 300.16 K
With the absolute temperature we can use <em>Charles' law </em>to solve this problem. This law states that at constant pressure:
Where in this case:
We input the data:
300.16 K * 1600 m³ = T₂ * 1250 m³
And solve for T₂:
T₂ = 384.2 K
