nsult the pKa values for certain functional groups on p. 57 of Bruice and then use the three dropdown menus to complete the statements below. I R R H3O+ action a would action b would OH action c would ROH RNH₂ RNH₂ R R H₂O OH + + + RO RNH3* RNH3*
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.
![Consult the pKa values for certain functional groups on p. 57 of Bruice and then use the three dropdown menus to complete the statements below.
a.
b.
C.
R
R
H3O+
Reaction a would
Reaction b would
OH
Reaction c would
+
ROH
+ RNH₂
+ RNH₂
R
R
H₂O
OH
+
RO
RNH3*
RNH3*](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F425a29c3-8b31-454d-8fec-dcd701a8f06d%2F39d438f0-1607-456c-b0e9-7aecb5010773%2Fz3p8j5d_processed.jpeg&w=3840&q=75)
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