
Interpretation:
Reaction between 1,3-Cyclopentadiene and cycloheptatrienone is suprafacial or antarafacial to give the product which is given below:
Concept introduction:
[6 + 4] Cycloaddition is a type of cycloaddition between a six-atom pi system and a four-atom pi system, leading to a ten-membered ring. It is a thermally allowed, higher-order cycloaddition process. Although most linear, acyclic trienes do not give [6 + 4] products selectively, cyclic trienes give high yields of [6 + 4] products in many cases.
A suprafacial cycloaddition occurs when like phases of the p orbitals of both reactants are on the same side of the pie system, so that two bonding interactions result.
An antarafacial cycloaddition occurs when one pie system must twist to align like phases of the p orbitals of the terminal carbons of the reactants.

Trending nowThis is a popular solution!

Chapter 30 Solutions
OWLv2 with Student Solutions Manual eBook, 4 terms (24 months) Printed Access Card for McMurry's Organic Chemistry, 9th
- Please see photoarrow_forward=Naming benzene derivatives Name these organic compounds: structure C1 CH3 name ☐ CH3 ப C1 × ☐arrow_forwardBlocking Group are use to put 2 large sterically repulsive group ortho. Show the correct sequence toconnect the reagent to product with the highest yield possible. * see image **NOTE: The compound on the left is the starting point, and the compound on the right is the final product. Please show the steps in between to get from start to final, please. These are not two different compounds that need to be worked.arrow_forward
- Nucleophilic Aromatic Substitution: What is the product of the reaction? What is the name of the intermediate complex? *See imagearrow_forwardPredict the final product. If 2 products are made, list which should be “major” and “minor” *see attachedarrow_forwardNucleophilic Aromatic Substitution: What is the product of the reaction? *see imagearrow_forward
- Show the correct sequence to connect the reagent to product. * see imagearrow_forwardThe answer here says that F and K have a singlet and a doublet. The singlet and doublet are referring to the H's 1 carbon away from the carbon attached to the OH. Why don't the H's two carbons away, the ones on the cyclohexane ring, cause more peaks on the signal?arrow_forwardDraw the Birch Reduction for this aromatic compound and include electron withdrawing groups and electron donating groups. *See attachedarrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning

