Acetylenic compounds may be used as dienophiles in the Diels-Alder reaction. Write the structure for an adduct that you expect f
rom the reaction of 1,3-butadiene with hexafluoro-2-butyne:
1 answer:
Answer:
Explanation:
An electron-donating heteroatom substituent at position-2 of a furan promotes regiospecific opening of the 7-oxa bridge of the Diels-Alder cycloadduct with hexafluoro-2-butyne, producing a 4-heterosubstituted 2,3-di(trifluoromethyl)phenol building block in a single step. The phenol and heteroatom substituent are easily transformed to the corresponding iodide or triflate that readily undergoes Heck, Suzuki, and Stille reactions to install a variety of substituents in high yields. This methodology provides a facile and general synthesis of 1,4-disubsituted 2, 3-di(trifluoromethyl)benzenes.
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Sodium(Na) is the limiting reagent.
<h3>What is Limiting reagent?</h3>The reactant that is totally consumed during a reaction, or the limiting reagent, decides when the process comes to an end. The precise quantity of reactant required to react with another element may be estimated from the reaction stoichiometry.
How do you identify a limiting reagent?
The limiting reactant is the one that is consumed first and sets a limit on the quantity of product(s) that can be produced. Calculate how many moles of each reactant are present and contrast this ratio with the mole ratio of the reactants in the balanced chemical equation to get the limiting reactant.
Start by writing the balanced chemical equation that describes this reaction
Notice that the reaction consumes 2 moles of sodium metal for every 1 mole of chlorine gas that takes part in the reaction and produces 2 moles of sodium chloride.
now we can see that we have 3 moles of sodium and 3 moles of chlorine, according to question. so, we can say that sodium is the limiting reagent in the given situation.
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