3. Consider the two substitution reactions shown below (A and B): A B XOXO H₂ D Br H₂ D Br H O D a. Assign every stereocenter in both of the starting materials and products above as either (R) or (S) configuration. Write your answers in the boxes above.
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.
answer part d and e for me please
![3. Consider the two substitution reactions shown below (A and B):
A
B
OX OX
H
O
D
a. Assign every stereocenter in both of the starting materials and products above as either (R) or (S)
configuration. Write your answers in the boxes above.
b. Provide a complete arrow pushing mechanism for each reaction. [Hint: Pay attention to the
product stereochemistry]
e. Write the rate law for reaction A.
c. In reaction B, a second isomeric product is expected to be formed in roughly equal amounts to
the product shown. Draw that second product, and label any stereocenters as (R) or (S).
d. What is the name of the mechanism that best describes these reactions?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F56fab682-21f0-4c9e-87de-cdb34e61df22%2F6542c7a2-6acd-470e-9ebc-397c07baa4a2%2F8e1fwhi_processed.jpeg&w=3840&q=75)
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