(80+125+45) / 10 = 250/10 =25
25 meters per minute= 0.41 meters/second
the direction and stopping time is irrelevant to the problem.
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
It would be the same amount. So, 45 ml of NaOH is required to be added to the 45 ml of HCI to neutralize the acid fully. Here is a brief calculation:
Firstly, here is your formula: M(HCI) x V(HCI) = M(NaOh) x V(NaOH)
With the values put in: 0.35 x 45 = 0.35 x V(NaOH)
= 45 ml.
There is 45 ml of V(NaOH)
Let me know if you need anything else. :)
- Dotz
Fix ur transition, it sounds choppy