Answer:
Here's what I get
Explanation:
(a) Intermediates
The three structures below represent one contributor to the resonance-stabilized intermediate, in which the lone pair electrons on the heteroatom are participating (the + charge on the heteroatoms do not show up very well).
(b) Relative Stabilities
The relative stabilities decrease in the order shown.
N is more basic than O, so NH₂ is the best electron donating group (EDG) and will best stabilize the positive charge in the ring. However, the lone pair electrons on the N in acetanilide are also involved in resonance with the carbonyl group, so they are not as available for stabilization of the ring.
(c) Relative reactivities
The relative reactivities would be
C₆H₅-NH₂ > C₆H₅-OCH₃ > C₆H₅-NHCOCH₃
Answer:
Al2(SO4)3 and Mg(OH)2
Explanation:
1. Al has a charge of 3-, and SO4 of 2-
when you cross multiply the charges you get
Al2 and (SO4)3
*the reason theres a bracket around the sulfate ion is that the charge 3 is not for oxygen only, but the entire sulphate ion*
Hence, Al2(SO4)3
2. Mg has a charge of 2- and OH of 1-
again cross multiply
Mg (you dont need to add the 1) and (OH)2
again, the bracket around OH means the charge appiles to Oxygen AND hydrogen
hence, Mg(OH)2
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