Among the three isomeric carbocations given below, [A / B / C] is expected to be the most stable one, and [A | B / C] is expected to be the least stable one. The more substituent attached to the positively charged carbon, the [more / less] electron density shifts toward the positive charge and the more [isomer / inductive / angle / steric / bond] stabilization of the cation occurs. do do A
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.
![2. Among the three isomeric carbocations given below, JA / B / C] is expected to be the most
stable one, and [A / B / C] is expected to be the least stable one. The more substituent
attached to the positively charged carbon, the [more / less] electron density shifts toward the
positive charge and the more [isomer / inductive / angle / steric / bond] stabilization of the
cation occurs.
A
B](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F662601a0-18b2-4601-928e-570472adf6eb%2Fa08b4571-6311-4bf5-81fd-365ee8d62878%2Fk9fr97f_processed.png&w=3840&q=75)
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