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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Answer:
I am not really sure, but I think Fr.
Explanation:
Answer:
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Explanation:
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__5___SiO2 + ___2___CaC2 → __5___Si + ____2___CaO + __4___CO2
Answer:
1.17 mol
Explanation:
Step 1: Write the balanced equation
2 Al + 6 HCl → 2 AlCl₃ + 3 H₂
Step 2: Calculate the moles corresponding to 85.0 g of HCl
The molar mass of HCl is 36.46 g/mol.
85.0 g × 1 mol/36.46 g = 2.33 mol
Step 3: Calculate the number of moles of H₂ produced from 2.33 moles of HCl
The molar ratio of HCl to H₂ is 6:3.
2.33 mol HCl × 3 mol H₂/6 mol H₂ = 1.17 mol H₂
