Show the mechanism for the following reaction: cyclohexene bromine yields a dibromocyclohexane Unlike previous problem, this pro
blem does require illustration of stereochemistry. Draw wedge-and-dash bond stereochemical structures – including H atoms on ALL chirality center (product and intermeidate both)– and include charges, electrons, and curved arrows. Details count. Draw one enantiomer only for any racemates. NOTE: A bromonium ion bromine should have TWO lone pairs, not three.
1 answer:
You might be interested in
The Molecule of Sodium Formate along with Formal Charges (in blue) and lone pair electrons (in red) is attached below.
Sodium Formate is an ionic compound made up of a positive part (Sodium Ion) and a polyatomic anion (Formate).
Nomenclature:
In ionic compounds the positive part is named first. As sodium ion is the positive part hence, it is named first followed by the negative part i.e. formate.
Name of Formate:
Formate ion has been derived from formic acid ( the simplest carboxylic acid). When carboxylic acids looses the acidic proton of -COOH, they are converted into Carboxylate ions.
E.g.
HCOOH (formic acid) → HCOO⁻ (formate) + H⁺
H₃CCOOH (acetic acid) → H₃CCOO⁻ (acetate) + H⁺
Formal Charges:
Formal charges are calculated using following formula,
F.C = [# of Valence e⁻] - [e⁻ in lone pairs + 1/2 # of bonding electrons]
For Oxygen:
F.C = [6] - [6 + 2/2]
F.C = [6] - [6 + 1]
F.C = 6 - 7
F.C = -1
For Sodium:
F.C = [1] - [0 + 0/2]
F.C = [1] - [0]
F.C = 1 - 0
F.C = +1
