Complete the mechanism for the reaction between acetone in acid and bromine by adding the missing bonds, atoms, o nonbonding electrons, and curved arrows (forward reaction only). Step 1 "poa Step 3: bromine is added. Complete the structure and add curved arrows. Select Draw Templates More CH Ĉ 10: Br 110111 ! H :—* CH Step 5: alter the water or bromide to give the final products. Select Draw Templates More Q2Q Br 14 Erese H Erase Step 2: complete the structure and add curved arrows. Select Draw Templates More INM Ć 0 Q2Q Step 4: complete the structure and add curved arrows. Select Drew Templates More H Erea Br Brass Q2Q
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.
![Complete the mechanism for the reaction between acetone in acid and bromine by adding the missing bonds, atoms, charges,
nonbonding electrons, and curved arrows (forward reaction only).
Step 1
"-"
H
10:
Ć
H
Step 3: bromine is added. Complete the structure
and add curved arrows.
Select Draw Templates More
H 0 Br
***
HO-H
1
H
Q2Q
Step 5: alter the water or bromide to give the
final products.
Select Draw Templates More
||||||||||| H
Br
Erase
HO:
H
Erase
pa
Step 2: complete the structure and add
curved arrows.
Select Draw Templates More
|||||||||| H
3
Select Draw Templates More
0
Step 4: complete the structure and add
curved arrows.
3 Ć
Q2Q
||||||||||| H 0 Br
H
Erase
**
Erase
aaª]](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff6ab806b-464c-4756-9d8f-72da0489465e%2F5101dd61-8596-4f3c-b6d6-35eabf780478%2Fb697e0w_processed.png&w=3840&q=75)
Trending now
This is a popular solution!
Step by step
Solved in 3 steps with 3 images
