Answer: (Structure attached).
Explanation:
This type of reaction is an aromatic electrophilic substitution. The overall reaction is the replacement of a proton (H +) with an electrophile (E +) in the aromatic ring.
The aromatic ring in p-fluoroanisole has two sustituents, an <u>halogen</u> and a <u>methoxy group</u>, which are <em>ortho-para</em> directing substituents.
Aryl sulfonic acids are easily synthesized by an electrophilic substitution reaction aromatic using <u>sulfur trioxide as an electrophile</u> (very reactive).
The reaction occurs in three steps:
- The attack on the electrophile forms the sigma complex.
- The loss of a proton regenerates an aromatic ring.
- The sulfonate group can be protonated in the presence of a strong acid (H₂SO₄).
Normally, a mixture of <em>ortho-para</em> substituted products would be obtained. However, since both <em>para</em> positions are occupied, only the <em>ortho </em>substituted product is obtained here.
For [Ni(en)³]²⁺ which is purple, the crystal field splitting energy is greater than the complex ion, [Ni(H₂O)₆]²⁺ which is green in color.
When a Lewis base id attached to the metal ion by covalent bond, then the complex ion is formed and when these complex ions are present with other ions of opposite charge or neutral charge, they will make complex compounds.
___AlBr3 + ___K -> ___KBr + ___ Al
1 AlBr3 + 3K -> 3KBr + 1 Al
hope this helps............
So the equation is balanced, meaning they have the smallest amounts of each element in the reactants to create the products.
So, 2 moles of H2S (the coefficient) contributes to 2 moles Ag2S, which is why the ratio is 2:2.
I hope that made sense.