Below is the free energy diagram for the substitution reaction of 2-chlorobutane with hydroxide ion: B Reaction coardinate Draw the structures, which correspond to A and C in the free-energy diagram above for the reaction of 2-chlorobutane with hydroxide ion. a. b. Label the free energy of activation (AG+) and free energy change AG°) on the diagram above. c. Is the reaction exergonic or endergonic (circle one)? page 4 of 17 Free energy
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.
![Below is the free energy diagram for the substitution reaction of 2-chlorobutane with
hydroxide ion:
Reaction coardinate
Draw the structures, which correspond to A and C in the free-energy diagram above
for the reaction of 2-chlorobutane with hydroxide ion.
a.
b. Label the free energy of activation (AG#) and free energy change AG") on the diagram
above.
c. Is the reaction exergonic or endergonic (circle one)?
page 4 of 17
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