Answer:
p-fluoronitrobenzene and sodium phenoxide is more appropriate
Explanation:
An ipso substitution is required to form p-nitrophenyl phenyl ether.
For this ipso substitution, an alkoxide anion needs to attack as a nucleophile at the carbon atom attached to fluorine atom and thereby substitute that F atom.
p-nitrophenoxide is an weak nucleophile as compared to phenoxide due to presence of electron withdrawing resonating effect of nitro group at para position.
p-fluoronitrobenzene is a good choice for nucleophilic attack by alkoxide anion as compared to fluorobenzene due to higher positive charge density at carbon atom directly attached to F atom. Higher positive charge density arises due to presence of electron withdrawing resonating effect og nitro group at para position.
So, p-fluoronitrobenzene and sodium phenoxide is more appropriate
Answer:
snetence
Explanation:
nikkak youk dxmbk aslk istgk
Answer : The heat of the reaction is -221.6 kJ
Explanation :
Heat released by the reaction = Heat absorbed by the calorimeter
where,
= heat released by the reaction = ?
= heat absorbed by the calorimeter
= specific heat of calorimeter = 
= change in temperature = 
Now put all the given values in the above formula, we get:
As,
So, 
Thus, the heat of the reaction is -221.6 kJ
Answer:
H⁺(aq) + H₂O(l) ⇄ H₃O⁺(aq)
Explanation:
According to Brönsted-Lowry acid-base theory, an acid is a substance that donates H⁺. Let's consider the molecular equation showing that benzoic acid is a Brönsted-Lowry acid.
C₆H₅COOH(aq) + H₂O(l) ⇄ C₆H₅COO⁻(aq) + H₃O⁺(aq)
The complete ionic equation includes all the ions and molecular species.
C₆H₅COO⁻(aq) + H⁺(aq) + H₂O(l) ⇄ C₆H₅COO⁻(aq) + H₃O⁺(aq)
The net ionic equation includes only the ions that participate in the reaction and the molecular species.
H⁺(aq) + H₂O(l) ⇄ H₃O⁺(aq)
I’m pretty sure it would be D.
