Multiple Choice
What is the IUPAC name of the compound with the structure ?
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Table of contents
- 1. A Review of General Chemistry5h 5m
- Summary23m
- Intro to Organic Chemistry5m
- Atomic Structure16m
- Wave Function9m
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- 2. Molecular Representations1h 14m
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- 4. Alkanes and Cycloalkanes4h 17m
- IUPAC Naming29m
- Alkyl Groups13m
- Naming Cycloalkanes10m
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- Naming Alkenes3m
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- Enantiomers vs. Diastereomers13m
- Atropisomers9m
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- Test 3:Disubstituted Cycloalkanes13m
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- 23. The Chemistry of Thioesters, Phophate Ester and Phosphate Anhydrides1h 10m
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- Tautomerization9m
- Tautomers of Dicarbonyl Compounds6m
- Enolate4m
- Acid-Catalyzed Alpha-Halogentation4m
- Base-Catalyzed Alpha-Halogentation3m
- Haloform Reaction8m
- Hell-Volhard-Zelinski Reaction3m
- Overview of Alpha-Alkylations and Acylations5m
- Enolate Alkylation and Acylation12m
- Enamine Alkylation and Acylation16m
- Beta-Dicarbonyl Synthesis Pathway7m
- Acetoacetic Ester Synthesis13m
- Malonic Ester Synthesis15m
- 25. Condensation Chemistry2h 9m
- 26. Amines1h 43m
- 27. Heterocycles2h 0m
- Nomenclature of Heterocycles15m
- Acid-Base Properties of Nitrogen Heterocycles10m
- Reactions of Pyrrole, Furan, and Thiophene13m
- Directing Effects in Substituted Pyrroles, Furans, and Thiophenes16m
- Addition Reactions of Furan8m
- EAS Reactions of Pyridine17m
- SNAr Reactions of Pyridine18m
- Side-Chain Reactions of Substituted Pyridines20m
- 28. Carbohydrates5h 53m
- Monosaccharide20m
- Monosaccharides - D and L Isomerism9m
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- 29. Amino Acids4h 20m
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- L and D Amino Acids14m
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- 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
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- Reactions of Amino Acids: Ninhydrin Test11m
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- Intro to Citric Acid Cycle7m
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- The Citric Acid Cycle35m
- 34. Nucleic Acids1h 32m
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- Electron Configuration of Elements45m
- Coordination Complexes20m
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- Electron Counting10m
- The 18 and 16 Electron Rule13m
- Cross-Coupling General Reactions40m
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- Kumada Coupling Reaction13m
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- Buchwald-Hartwig Amination Reaction19m
- Eglinton Reaction17m
- Catalytic Allylic Alkylation18m
- Alkene Metathesis23m
- 36. Synthetic Polymers1h 49m
- Introduction to Polymers6m
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- Polymers Structure and Properties8m
4. Alkanes and Cycloalkanes
IUPAC Naming
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 IUPAC name for the product formed when reacts with aqueous under reflux conditions?
A
(ethene)
B
(chloroethane)
C
(ethane)
D
(ethanol)
Verified step by step guidance1
Identify the starting material: C\_2H\_5Br is bromoethane, an alkyl halide where a bromine atom is attached to an ethyl group.
Recognize the reagent and conditions: aqueous KOH under reflux typically promotes nucleophilic substitution reactions, where the hydroxide ion (OH\^-) acts as a nucleophile.
Determine the type of reaction: since the solvent is aqueous and the conditions are reflux, the reaction proceeds mainly via an SN2 mechanism, where OH\^- replaces Br in bromoethane.
Write the substitution reaction: C\_2H\_5Br + OH\^- \rightarrow C\_2H\_5OH + Br\^- , where the bromine atom is replaced by a hydroxyl group, forming an alcohol.
Name the product using IUPAC rules: the product is an ethyl group attached to a hydroxyl group, which is named ethanol.
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