Draw the product of the reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore inorganic byproducts.
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.
![Chrome File Edit View History Bookmarks Profiles Tab Window Help
28 University of Roches X
Kinesis scolarship
app.101edu.co
Meliora! - FAOnline
UUU
.
olelebababal
Inbox (4) - isanche7 X
A
Neuromedicine -...
Drawing
O
Inbox - snivana24@ X
Neuromedicine -...
Food for Thought -
Study Abroad
×
Applying to Medic...
Problem 53 of 18
Atoms, Bonds
and Rings
JAN
A 28
Charges
Activity Stream
Draw or tap a new bond to see suggestions.
tv
Blueprint MCATⓇ...
X
Aktiv Chemistry
Practice Passages...
W
P
W
X
Q8
b Success Confirmatio X
Chemistry Bootca...
Undo
(x)
Remove
Reset
Done
▬▬
● Sat Jan 28 4:40 PM
6
+
>>
Submit
Drag To Pan
+](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa44093f9-865e-42e2-9761-7238b47b32ab%2F115f3d22-91af-4601-9e03-e02a8f74c750%2F0ewfag9_processed.png&w=3840&q=75)
![Chrome File Edit View History Bookmarks Profiles
28 University of Roches X
Kinesis scolarship
app.101edu.co
Meliora! - FAOnline
UUL
olebababababal
Inbox (4) - isanche7 X
+
Neuromedicine -...
Draw the product of the reaction shown below. Use a dash or wedge bond
to indicate stereochemistry of substituents on asymmetric centers, Ignore
inorganic byproducts.
Tab Window Help
O
Inbox - snivana24@ X
Neuromedicine -...
Food for Thought -
Study Abroad
×
Applying to Medic...
Problem 53 of 18
Atoms, Bonds
and Rings
JAN
A 28
Charges
Activity Stream
Draw or tap a new bond to see suggestions.
tv
Blueprint MCATⓇ...
X
Aktiv Chemistry
Practice Passages...
W
P
W
X
Q8
b Success Confirmatio X
Chemistry Bootca...
Undo
(x)
Remove
Reset
Done
▬▬
● Sat Jan 28 4:40 PM
6
+
>>
Submit
Drag To Pan
+](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa44093f9-865e-42e2-9761-7238b47b32ab%2F115f3d22-91af-4601-9e03-e02a8f74c750%2F2pswzb_processed.png&w=3840&q=75)
![](/static/compass_v2/shared-icons/check-mark.png)
Step by step
Solved in 2 steps with 2 images
![Blurred answer](/static/compass_v2/solution-images/blurred-answer.jpg)
![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9781305080485/9781305080485_smallCoverImage.gif)
![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9781305080485/9781305080485_smallCoverImage.gif)