Textbook Question
Predict the product of the following reaction sequences.
(c)
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- 1. A Review of General Chemistry5h 5m
- Summary23m
- Intro to Organic Chemistry5m
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- 25. Condensation Chemistry2h 9m
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- 27. Heterocycles2h 0m
- Nomenclature of Heterocycles15m
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- Disaccharide30m
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- 29. Amino Acids4h 20m
- Proteins and Amino Acids19m
- L and D Amino Acids14m
- Polar Amino Acids14m
- Amino Acid Chart1h 18m
- Acid-Base Properties of Amino Acids33m
- Isoelectric Point14m
- Amino Acid Synthesis: HVZ Method12m
- Synthesis of Amino Acids: Acetamidomalonic Ester Synthesis16m
- Synthesis of Amino Acids: N-Phthalimidomalonic Ester Synthesis13m
- Synthesis of Amino Acids: Strecker Synthesis13m
- Reactions of Amino Acids: Esterification7m
- Reactions of Amino Acids: Acylation3m
- Reactions of Amino Acids: Hydrogenolysis6m
- Reactions of Amino Acids: Ninhydrin Test11m
- 30. Peptides and Proteins2h 42m
- Peptides12m
- Primary Protein Structure4m
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- Quaternary Protein Structure10m
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- Intro to Peptide Sequencing2m
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- Peptide Sequencing: Partial Hydrolysis with Cyanogen Bromide7m
- Peptide Sequencing: Edman Degradation28m
- Merrifield Solid-Phase Peptide Synthesis18m
- 31. Catalysis in Organic Reactions1h 30m
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- 33. The Organic Chemistry of Metabolic Pathways2h 52m
- Intro to Metabolism6m
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- Intro to Glycolysis3m
- Catabolism of Carbohydrates: Glycolysis27m
- Glycolysis Summary15m
- Pyruvate Oxidation (Simplified)4m
- Anaerobic Respiration11m
- Catabolism of Fats: Glycerol Metabolism11m
- Intro to Citric Acid Cycle7m
- Structures of the Citric Acid Cycle19m
- The Citric Acid Cycle35m
- 34. Nucleic Acids1h 32m
- 35. Transition Metals6h 14m
- Electron Configuration of Elements45m
- Coordination Complexes20m
- Ligands24m
- Electron Counting10m
- The 18 and 16 Electron Rule13m
- Cross-Coupling General Reactions40m
- Heck Reaction40m
- Stille Reaction13m
- Suzuki Reaction25m
- Sonogashira Coupling Reaction17m
- Fukuyama Coupling Reaction15m
- Kumada Coupling Reaction13m
- Negishi Coupling Reaction16m
- Buchwald-Hartwig Amination Reaction19m
- Eglinton Reaction17m
- Catalytic Allylic Alkylation18m
- Alkene Metathesis23m
- 36. Synthetic Polymers1h 49m
- Introduction to Polymers6m
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- Radical Polymerization15m
- Cationic Polymerization8m
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- Polymer Stereochemistry3m
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- Copolymers6m
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- Step-Growth Polymers: Urethane6m
- Step-Growth Polymers: Polyurethane Mechanism10m
- Step-Growth Polymers: Epoxy Resin8m
- Polymers Structure and Properties8m
13. Alcohols and Carbonyl Compounds
Reducing Agent
Struggling with Organic Chemistry?
Join thousands of students who trust us to help them ace their exams!Watch the first videoMultiple Choice
What is the product of the reacion?
A
B
C
D
No reaction
Verified step by step guidance1
Identify the functional group in the starting material. The starting material is a lactone, which is a cyclic ester.
Consider the reagent used in the reaction. Sodium borohydride (NaBH4) is a reducing agent commonly used to reduce aldehydes and ketones to alcohols.
Evaluate the reactivity of the functional group with the reagent. NaBH4 is not strong enough to reduce esters or lactones under normal conditions.
Conclude that since the lactone is not reactive with NaBH4, no reaction will occur.
Understand that the correct answer is 'No reaction' because the lactone remains unchanged in the presence of NaBH4.
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