The Answer for this question is : A
1 & 2
Explanation:
yes you got the right idea
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
The nurse<span> is </span>caring<span> for a </span>client<span> with a temperature of 104.5 degrees Fahrenheit. A health </span>care provider<span> prescribes 500 mg of an antibiotic intravenous While undergoing a soapsuds </span>enema, theclient reports abdominal<span> cramping.</span>