Modify the given copies of the starting materials to draw the major product(s) for the following Diels-Alder reaction. Use the single bond tool to interconvert between double and single bonds, and use wedges and dashes to indicate the stereochemistry of any newly formed chiral centers. If a pair of enantiomers is expected, be sure to draw both enantiomers. Note: you can save time drawing by selecting a structure and using the copy/paste function.
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.
![Modify the given copies of the starting materials to draw the major product(s) for the following Diels-Alder reaction. Use the
single bond tool to interconvert between double and single bonds, and use wedges and dashes to indicate the stereochemistry of
any newly formed chiral centers. If a pair of enantiomers is expected, be sure to draw both enantiomers. Note: you can save time
drawing by selecting a structure and using the copy/paste function.
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