Draw the organic product(s) of the following reaction. CH₂ H₂C-CH-CEC-H Vt/85 0 You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Nat in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu. ▼ / KO-t-Bu/1-BuOH tois 24 //.000. [
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.
![[Review Topics]
Draw the organic product(s) of the following reaction.
CH
H₂C-CH-CEC-H
You do not have to consider stereochemistry.
• Include cationic counter-ions, e.g., Nat in your answer, but draw them in their own
sketcher.
If no reaction occurs, draw the organic starting material.
• Separate multiple products using the + sign from the drop-down menu.
Show Transcribed Text
.
KO-t-Bu/1-BUOH
8
.
මැමැණි.
///.000. It
vornew ropios
Draw the organic product(s) of the following reaction.
CEC-H
[References]
Ĉ
KO--BU-BUOH
• You do not have to consider stereochemistry.
Include cationic counter-ions, e.g... Nat in your answer, but draw them in their own
sketcher.
[Konterences]
If no reaction occurs, draw the organic starting material
• Separate multiple products using the sign from the drop-down menu.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F77b64fd0-733a-42da-88f3-0e07ab6f0a8f%2F1fe148d8-0196-4e65-90e4-257bf0606fab%2Fvjdnfdi_processed.png&w=3840&q=75)
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