I can’t see it so u won’t get and answer
Answer:
1600
Explanation:
5×10^4÷2.5×10^2
(5×10^4)
(10^4)
(5×40)
(200)
(200÷2.5)
(80)
(80×10^2)
(10^2)
(20)
(80×20)
Answer is 1600.
Sorry if it's not correct.
You put precipitation in the wrong place the answer is D+A (number 4)
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:
Carbon dioxide is a linear covalent molecule.
Carbon dioxide is an acidic oxide and reacts with water to give carbonic acid.
CO 2 + H2O ==> H2CO3
Carbon dioxide reacts with alkalis to give carbonates and bicarbonates.
CO 2 + NaOH ==> NaHCO3 (Sodium BiCarbonate )
NaHCO3 + NaOH ==> Na2CO3 (Sodium Carbonate) + H2O