Be sure to answer all parts. Draw the products formed, disregarding stereoisomers, when the following alkene is treated with NBS + hv. Part 1: CH3CH₂CH=CHCH₂CH3 Two product(s) is/are formed, disregarding stereoisomers. Only consider constitutional isomers; ignore stereoisomers. Part 2 out of 2 Draw the two different constitutional isomers. Stereochemistry is not necessary. draw structure... (original C=C) draw structure... (migrated C=C)
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.
#14
![Be sure to answer all parts.
Draw the products formed, disregarding stereoisomers, when the following alkene is treated with
NBS + hv.
Part 1:
CH3CH₂CH=CHCH₂CH3
Two
product(s) is/are formed, disregarding stereoisomers. Only consider constitutional isomers;
ignore stereoisomers.
Part 2 out of 2
Draw the two different constitutional isomers. Stereochemistry is not necessary.
draw structure...
(original C=C)
I
draw structure ...
(migrated C=C)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F7c8f01e2-a14e-48cc-8752-a6869fe4cc3e%2F1d70788a-18b7-49bb-818a-987a2d997dc9%2F7xqhwk_processed.png&w=3840&q=75)
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