Table of contents

1. A Review of General Chemistry5h 5m
2. Molecular Representations1h 14m
3. Acids and Bases2h 46m
4. Alkanes and Cycloalkanes4h 17m
5. Chirality3h 39m
6. Thermodynamics and Kinetics1h 22m
7. Substitution Reactions1h 48m
8. Elimination Reactions2h 30m
9. Alkenes and Alkynes2h 9m
10. Addition Reactions3h 19m
11. Radical Reactions1h 58m
12. Alcohols, Ethers, Epoxides and Thiols2h 42m
13. Alcohols and Carbonyl Compounds2h 17m
14. Synthetic Techniques1h 26m
15. Analytical Techniques:IR, NMR, Mass Spect7h 3m
16. Conjugated Systems6h 13m
17. Ultraviolet Spectroscopy51m
18. Aromaticity2h 34m
19. Reactions of Aromatics: EAS and Beyond5h 1m
20. Phenols55m
21. Aldehydes and Ketones: Nucleophilic Addition4h 56m
22. Carboxylic Acid Derivatives: NAS2h 51m
23. The Chemistry of Thioesters, Phophate Ester and Phosphate Anhydrides1h 10m
24. Enolate Chemistry: Reactions at the Alpha-Carbon1h 53m
25. Condensation Chemistry2h 9m
26. Amines1h 43m
27. Heterocycles2h 0m
28. Carbohydrates5h 53m
29. Amino Acids4h 20m
30. Peptides and Proteins2h 42m
31. Catalysis in Organic Reactions1h 30m
32. Lipids 2h 50m
33. The Organic Chemistry of Metabolic Pathways2h 52m
34. Nucleic Acids1h 32m
35. Transition Metals6h 14m
36. Synthetic Polymers1h 49m

16. Conjugated Systems

Diels-Alder Forming Bridged Products

Organic Chemistry

16. Conjugated Systems

Diels-Alder Forming Bridged Products

Previous problemNext problem

2:59 minutes

Problem 44b

Textbook Question

What are the products of the following reactions?
b.

Verified step by step guidance

Identify the type of reaction taking place. For example, determine if it is a substitution, elimination, addition, or rearrangement reaction. This will depend on the reactants and reaction conditions provided in the problem.

Analyze the structure of the reactants. Look for functional groups, double or triple bonds, and any stereochemistry that might influence the reaction pathway.

Consider the reaction conditions (e.g., reagents, solvents, temperature, and catalysts). These will help you predict the mechanism and the products. For example, the use of a strong base might suggest an elimination reaction, while an acid catalyst might indicate an addition reaction.

Write out the mechanism step by step. Show how bonds are broken and formed, and use curved arrows to indicate the movement of electrons. This will help you visualize the intermediates and transition states.

Determine the final products by completing the reaction mechanism. Ensure that you account for all atoms and charges, and check for any stereochemical outcomes if applicable.

Verified video answer for a similar problem:

This video solution was recommended by our tutors as helpful for the problem above

Video duration:

Play a video:

Was this helpful?

Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Reaction Mechanisms

Understanding reaction mechanisms is crucial in organic chemistry as they describe the step-by-step process by which reactants transform into products. This includes identifying intermediates, transition states, and the movement of electrons. A clear grasp of mechanisms helps predict the products of reactions and the conditions under which they occur.

Functional Groups

Functional groups are specific groups of atoms within molecules that are responsible for the characteristic chemical reactions of those molecules. Recognizing functional groups is essential for predicting the behavior of organic compounds during reactions, as they dictate reactivity and the types of products formed.

Stoichiometry

Stoichiometry involves the calculation of reactants and products in chemical reactions. It is essential for determining the amounts of substances consumed and produced, allowing chemists to predict yields and understand the proportions in which reactants react. Mastery of stoichiometry is vital for balancing chemical equations and optimizing reaction conditions.

Watch next

Master Bridged-Products with a bite sized video explanation from Johnny

Start learning

Related Videos

Related Practice

Textbook Question

Furan and maleimide undergo a Diels–Alder reaction at 25 °C to give the endo isomer of the product. When the reaction takes place at 90 °C, however, the major product is the exo isomer. Further study shows that the endo isomer of the product isomerizes to the exo isomer at 90 °C.

c. Examine your answer to (b) and determine whether this answer applies to a reaction that is kinetically controlled or one that is thermodynamically controlled, or both.

Multiple Choice

Predict the major, organic product for the following reaction.

Textbook Question

While attempting to recrystallize maleic anhydride, a student dissolved it in freshly distilled cyclopentadiene rather than in freshly distilled cyclopentane. Was her recrystallization successful?

Textbook Question

What are the products of the following reactions?

Textbook Question

Predict the products of the following proposed Diels–Alder reactions.

(e)

Textbook Question

Predict the products of the following proposed Diels–Alder reactions.

(d)

Textbook Question

Predict the products of the following proposed Diels–Alder reactions.

(c)

Textbook Question