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Draw the major product (constitutional isomer) formed when the reactant shown is hydrogenated with one equivalent of H2 in th presence of a palladium catalyst. Do not depict the configuration(s) of any stereogenic center(s) that would result. If a mixture of constitutional isomers would result, draw the product that would form in the greatest amount. H2 (1 equivalent) Pd

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.

Draw the major product (constitutional isomer) formed when the reactant shown is hydrogenated with one equivalent of H₂ in the
presence of a palladium catalyst. Do not depict the configuration(s) of any stereogenic center(s) that would result. If a mixture of
constitutional isomers would result, draw the product that would form in the greatest amount.
H₂ (1 equivalent)
Pd

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