Answer:
Determine a detailed mechanism for the chlorination of benzene using cl2 and fecl3.
1 answer:
Step (1):
Generation of electrophile: by the action of Lewis acid FeCl₃ on Cl₂ to serve as a source of Cl⁺ (Electrophile)
Step (2):
Addition of electrophile to form carbocation:
addition of electrophile to form C-Cl bond and form carbocation which is stabilized by resonance.
Step (3):
Loss of proton to re-form the aromatic ring by the action of FeCl₄⁻ which removes proton from carbon containing Cl and forming the aromatic ring again
Generation of electrophile: by the action of Lewis acid FeCl₃ on Cl₂ to serve as a source of Cl⁺ (Electrophile)
Step (2):
Addition of electrophile to form carbocation:
addition of electrophile to form C-Cl bond and form carbocation which is stabilized by resonance.
Step (3):
Loss of proton to re-form the aromatic ring by the action of FeCl₄⁻ which removes proton from carbon containing Cl and forming the aromatic ring again
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Visual representation of covalent bonding indicating the valence shell electrons in the molecule, lines represents the shared pair of electron and pair of electrons that are not involved in bonding are represented as dots(lone pairs) are known as Lewis structures.
Compound formation takes place in order to complete the octet of each element that is according to octet rule, each atom forms bond with other atom in order to complete their octet that is to get eight electrons in its valence shell and attain stability.
An organic compound of the form is known as ketene.
The given ketene is .
The number of valence electron of:
The number of valence electrons in =
2 electrons are involved in each single bond between carbon and hydrogen and 4 electrons are involved in each double bond formed between carbon-carbon and carbon-oxygen. Hence, the total number of electrons involved in bond formation are 12 and rest 2 pair of electrons are present on oxygen as lone pair of electrons.
Therefore, the attached image is the Lewis structure of .
