Predict the major, organic product for the following reaction. <img src="https://media.pearsoncmg.com/ph/esm/ecs_mullins_organic1e/msa/content/practice-test/img/Ch10_Q07_QT.jpg" alt="The figure illustrates a reaction. The reaction contains three reactants. The first reactant has the following structure: A 7-carbon alkyne chain is depicted as a line structure using 2 zigzag lines from C 1 to C 3, three parallel lines between C 3 and C 4, and 3 zigzag lines from C 4 to C 7. C 2 is single bonded to C H 3 on the upper left in the form of a line. The second reactant is N a superscript zero written over the reaction arrow. The third reactant is N H 3 written under the reaction arrow." />

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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

9. Alkenes and Alkynes

Hydrogenation of Alkynes

Organic Chemistry

9. Alkenes and Alkynes

Hydrogenation of Alkynes

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Multiple Choice

Predict the major, organic product for the following reaction.

The figure illustrates the structure of a molecule. A 7-carbon alkene chain is depicted as a line structure using 6 zigzag lines. A double bond is present between C 3 and C 4. C 2 is single bonded to C H 3 below in the form of a line.

The figure illustrates the structure of a molecule. A 7-carbon alkane chain is depicted as a line structure using 6 zigzag lines. C 2 is single bonded to C H 3 below in the form of a line.

The figure illustrates the structure of a molecule. A 7-carbon alkene chain is depicted as a line structure using 2 zigzag lines from C 1 to C 3, two parallel lines between C 3 and C 4, and 3 zigzag lines from C 4 to C 7. C 2 is single bonded to C H 3 on the lower right in the form of a line.

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Verified step by step guidance

Identify the type of reaction: The reaction involves an alkyne and the reagents sodium (Na) and ammonia (NH3), which is indicative of a dissolving metal reduction, specifically the Birch reduction.

Understand the mechanism: In a Birch reduction, an alkyne is reduced to a trans-alkene. Sodium donates electrons to the alkyne, and ammonia provides protons, leading to the formation of a trans-alkene.

Analyze the starting material: The starting material is a terminal alkyne with a branched alkyl group. The triple bond is the site of reduction.

Predict the product: The alkyne will be reduced to a trans-alkene. The major product will have the double bond in a trans configuration, maintaining the original carbon skeleton.

Consider stereochemistry: Ensure that the resulting alkene has the correct stereochemistry, with substituents on opposite sides of the double bond, resulting in a more stable trans-alkene.