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:
a. eletrophile
b. able to impose regioselectivity and stereo selectivity.
c. faster
Explanation:
Necleophile reaction is chemical reaction in which electron rich chemical specie replaces functional group with another electron deficient molecule. Lewis acid catalyst is organic chemical reaction which lewis acid act as electron pair acceptor. Nucleophile reaction proceeds about 25 times more faster than benzene.
Answer:

Explanation:
Ba(OH)₂ + 2HCl ⟶ BaCl₂ + H₂O
V/mL: 249
c/mol·L⁻¹: 0.0443 0.285
1. Calculate the moles of Ba(OH)₂

2. Calculate the moles of HCl
The molar ratio is 2 mol HCl:1 mol Ba(OH)₂

3. Calculate the volume of HCl

Answer:
Argon
Explanation:
It has more electron than chlorine
A positive change atom of hydrogen-ion. A normal hydrogen atomic nucleus