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.
Answer:It would never stop until something hit the ball, to slow it down.
Explanation:
This is so because there is no gravitational pull in space.
Answer:

Explanation:
The formula for molality is:

There are 0.210 moles of KBr and 0.075 kilograms of pure water.

Substitute the values into the formula.

Divide.

The molality is <u>2.8 moles per kilogram</u>