Assume, in this context, that the methoxy group is sterically smaller than the methyl group, an assumption that is supported by the fact that methoxy groups induce less axial strain than methyl groups in cyclohexane conformations. H H CH₂ Most stable H₂C cond most stable ast stable H H B CH₂ OCH OCH₂ H₂C HH C een Хроно H₂C CH₂ D [Choose] [Choose] [Choose] HH DOCHS H₂C H₂C H H F OCH₂
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.
![Identify the most stable, second most stable, and least stable conformation
resulting from rotation about the bond indicated by the purple arrow.
Assume, in this context, that the methoxy group is sterically smaller than the
methyl group, an assumption that is supported by the fact that methoxy
groups induce less axial strain than methyl groups in cyclohexane
conformations.
H
H CH₂
CH₂
QOCH, HIC DOCH, HIC
H₂C
H₂C
A
Most stable
Second most stable
OCH₂
Least stable
HH
с
H₂
OCH H₂C
[Choose]
[Choose]
[Choose ]
OCH₂
CH₂
D
H₂C+
HH
носна
H₂C
H₂C
H
H
H
OCH₂](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F2dfaa744-8b25-46bc-9632-9166932aebcb%2Fe3b7b12c-a8f4-495e-a938-852e9c384c20%2Ftptdekf_processed.jpeg&w=3840&q=75)
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