Draw an appropriate reactant on the left-hand side of this organic reaction. Also, if any additional major products will be formed, add them to the right-hand side of the reaction. C+ C™ Click and drag to start drawing a structure. :0 + T X 1. Oso $ 2. NaHSO3 H₂O OH OH ?圖 clo Ar
Reactive Intermediates
In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.
Hydride Shift
A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.
Vinylic Carbocation
A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.
Cycloheptatrienyl Cation
It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.
Stability of Vinyl Carbocation
Carbocations are positively charged carbon atoms. It is also known as a carbonium ion.
![Draw an appropriate reactant on the left-hand side of this organic reaction.
Also, if any additional major products will be formed, add them to the right-hand side of the reaction.
C+
C™
Click and drag to start
drawing a structure.
с
+
X
1. Oso
$
2. NaHSO3 H₂O
C
OH
OH
clo](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F593e4a4c-a9fc-4231-bacd-fbc9affb1612%2Fed45db30-bc8e-45e6-9039-40fd2adfdca5%2Fb7rvjpp8_processed.jpeg&w=3840&q=75)
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