Show how you might synthesize this compound from an alkyl bromide and a nucleophile in an SN2 reaction. مل Submit Answer • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Only draw the reactants. Separate multiple reactants using the + sign from the drop-down menu. • If there is more than one possible combination of alkyl bromide and nucleophile, draw only one combination. . Do not include counter-ions, e.g., Na+, I, in your answer. N3 85 ChemDoodleⓇ Retry Entire Group O-Sn [F C 8 more group attempts remaining
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.
![Show how you might synthesize this compound from an alkyl bromide and a nucleophile in an SN2 reaction.
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من
• Use the wedge/hash bond tools to indicate stereochemistry where it exists.
• Only draw the reactants. Separate multiple reactants using the + sign from the drop-down menu.
• If there is more than one possible combination of alkyl bromide and nucleophile, draw only one combination.
• Do not include counter-ions, e.g.,
Na+, I, in your answer.
Submit Answer
N3
?
ChemDoodle
Retry Entire Group
▼n
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8 more group attempts remaining](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd72a3123-7c63-4e48-96b9-2d394375b3c8%2Fae513ab3-c93c-42ab-800e-3732e1fe5e9a%2Fxd7gsm4_processed.jpeg&w=3840&q=75)
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