Draw the structure(s) of the major organic product(s) of the following reaction. NH₂ NaNO₂ aqueous HCI at 0° NC • You do not have to consider stereochemistry. • Include counter-ions, e.g., Na+, I, in your submission, but draw them in their own separate sketcher. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ● Separate multiple products using the + sign from the drop-down menu.
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.
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![Draw the structure(s) of the major organic product(s) of the following reaction.
NH₂
NaNO₂
aqueous HCI at 0°
NC
• You do not have to consider stereochemistry.
• Include counter-ions, e.g., Na+, I, in your submission, but draw them in their own separate sketcher.
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
●
Separate multiple products using the + sign from the drop-down menu.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc1eb37bf-1045-43dd-a351-de2d9ca4d2a5%2F212c34a2-9bfc-4341-8518-c91aa4862e05%2F6hprlm_processed.jpeg&w=3840&q=75)
![Draw the structure(s) of the major neutral organic product(s) obtained after workup of the following reaction.
COOH
"NH₂
●
2 eq. Cl₂
• You do not have to consider stereochemistry.
• If no reaction occurs, draw the organic starting material.
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
Separate multiple products using the + sign from the drop-down menu.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc1eb37bf-1045-43dd-a351-de2d9ca4d2a5%2F212c34a2-9bfc-4341-8518-c91aa4862e05%2F4gzha1r_processed.jpeg&w=3840&q=75)
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