Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive. Since soft nucleophiles are less strongly solvated than hard nucleophiles, these solvents boost the relative reactivity of soft anions.
<h3>
Ethanol is either a nucleophile or a base.</h3>
The ethanol is a base Because carbocation is an extremely reactive species, a base or nucleophile as weak as ethanol can replace or remove it. SN1 and E1 would not be conceivable without the carbocation or a strong departing group.
<h3>How do solvents impact anionic nucleophile's reactivity?</h3>
In polar aprotic solvents, nucleophilic substitution reactions of anionic nucleophiles often proceed more quickly. The normal relative reactivity order in such solvents (like DMSO)is Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive.
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You can have as many controls as necessary, But they must remain equal at all times in order to get the most accurate results
Answer:
0.145 moles de AlBr3.
Explanation:
¡Hola!
En este caso, al considerar la reacción química dada:
Al(s)+Br2(l)⟶AlBr3(s)
Es claro que primero debemos balancearla como se muestra a continuación:
2Al(s)+3Br2(l)⟶2AlBr3(s)
Así, calculamos las moles del producto AlBr3 por medio de las masas de ambos reactivos, con el fin de decidir el resultado correcto:
Así, inferimos que el valor correcto es 0.145 moles de AlBr3, dado que viene del reactivo límite que es el aluminio.
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To make a supersaturated solution<span>, make a saturated </span>solution<span> of sugar by adding 360 grams of sugar to 100 mL of water at 80 degrees Celsius. When the water cools back down to 25 degrees, that 360 grams of sugar will still be dissolved even though the water </span>should<span> only dissolve 210 grams of sugar.</span>
