5. Draw the Birch reduction reactions of: a) fluorobenzene b) aniline Specify the mechanism, reaction conditions and final products. How does the electronic arrangement of a starting compounds impact the structure of a product?
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.
please do each and every part of question, do not give incomplete answer . Along with mechanism reaction plz aslo ans the last part of question that is " how does electronic arrange ..."
Do complete question , i will upvote
![5. Draw the Birch reduction reactions of:
a) fluorobenzene
b) aniline
Specify the mechanism, reaction conditions and final products. How does the
electronic arrangement of a starting compounds impact the structure of a
product?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F130d1251-1f74-4974-84f4-6d92cfa84e59%2F391154a7-66b4-46a5-9744-9b040bfe88d5%2Fhagae0p_processed.jpeg&w=3840&q=75)
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