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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:
See the images below
Step-by-step explanation:
To draw a dot diagram of an atom, you locate the element in the Periodic Table and figure out how many valence electrons it has. Then you distribute the electrons as dots around the atom,
a. Silicon.
Si is in Group 14, so it has four valence electrons.
b. Xenon
Xenon is in Group 18, so it has eight valence electrons. We group them as four pairs around the xenon atom.
c. Calcium
Calcium is in Group 2, so it has two valence electrons. They are in a single subshell, so we write them as a pair on the calcium atom.
d. Water
Oxygen is in Group 16, so it has six valence electrons. The hydrogen atoms each contribute one electron, so there are eight valence electrons.
Chemists often use a dash to represent a pair of electrons in a bond.
