Br а сHз b a d c b CH3-C-CH2-CH3 e CH-0-CH2-CH2-CH3 Br a CH3 Signal "a" Signal "a" Signal "b" Signal "b" Signal "c" Signal "d" Signal "c" Signal "e"
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.
Indicate the multiplicity (singlet, doublet, triplet, quartet, quintet, sextet, septet, multiplet,
etc.) of each signal in the HNMR spectrum of each of the following compounds:
![Br
а сHз
b a
d c
b
CH3-C-CH2-CH3
e CH-0-CH2-CH2-CH3
Br
a CH3
Signal "a"
Signal "a"
Signal "b"
Signal "b"
Signal "c"
Signal "d"
Signal "c"
Signal "e"](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F4b6078a5-5329-4ddc-8cf0-0c10f5757356%2F8c50cc46-628a-4057-a56b-ae18232d2e20%2Fylcmj0o_processed.png&w=3840&q=75)
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