G elec G 3,3-| G 2-m Add Gwha Peri QWh Cur G how takeAssignment/takeCovalentActivity.do?locator-assignment-take [References) Draw a structural formula for the more stable carbocation intermediate formed in the reaction shown HCI You do not have to consider stereochemistry Do not include anionic counter-ions, e g., r, in your answwer For cases in wvhich carbocations of the same or similar stability are expected, draw all of the Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the Separate structures with + signs from the drop-down menu. O00-h
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.
draw a structural formula for the more stable carbocation intermediate formed in the reaction shown
![G elec G 3,3-| G 2-m
Add Gwha
Peri QWh Cur G how
takeAssignment/takeCovalentActivity.do?locator-assignment-take
[References)
Draw a structural formula for the more stable carbocation intermediate formed in the reaction shown
HCI
You do not have to consider stereochemistry
Do not include anionic counter-ions, e g., r, in your answwer
For cases in wvhich carbocations of the same or similar stability are expected, draw all of the
Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the
Separate structures with + signs from the drop-down menu.
O00-h](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F70f35139-52c8-4887-96dd-7a5ffbf5fa5e%2F8746b295-79c9-4969-9377-b820aa324612%2Fbxsyt2e.jpeg&w=3840&q=75)
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