Ch. 11 - Radical ReactionsWorksheetSee all chapters
All Chapters
Ch. 1 - A Review of General Chemistry
Ch. 2 - Molecular Representations
Ch. 3 - Acids and Bases
Ch. 4 - Alkanes and Cycloalkanes
Ch. 5 - Chirality
Ch. 6 - Thermodynamics and Kinetics
Ch. 7 - Substitution Reactions
Ch. 8 - Elimination Reactions
Ch. 9 - Alkenes and Alkynes
Ch. 10 - Addition Reactions
Ch. 11 - Radical Reactions
Ch. 12 - Alcohols, Ethers, Epoxides and Thiols
Ch. 13 - Alcohols and Carbonyl Compounds
Ch. 14 - Synthetic Techniques
Ch. 15 - Analytical Techniques: IR, NMR, Mass Spect
Ch. 16 - Conjugated Systems
Ch. 17 - Aromaticity
Ch. 18 - Reactions of Aromatics: EAS and Beyond
Ch. 19 - Aldehydes and Ketones: Nucleophilic Addition
Ch. 20 - Carboxylic Acid Derivatives: NAS
Ch. 21 - Enolate Chemistry: Reactions at the Alpha-Carbon
Ch. 22 - Condensation Chemistry
Ch. 23 - Amines
Ch. 24 - Carbohydrates
Ch. 25 - Phenols
Ch. 26 - Amino Acids, Peptides, and Proteins

Isomers of Radical Halogenation

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Sections
Radical Reaction
Radical Stability
Free Radical Halogenation
Radical Selectivity
Calculating Radical Yields
Anti Markovnikov Addition of Br
Free Radical Polymerization
Allylic Bromination
Radical Synthesis
Additional Practice
Isomers of Radical Halogenation
Radical Hydrohalogenation of Alkynes
Alkyl Halide Radical Reduction
Ether Autooxidation
Cyclopropane as a Nucleophile
Radical Disproportionation
Radical Texas Two-Step
Radical Retrosynthesis
Additional Practice

Solution: How many monochloro substitution products are produced when the alkanes below are chlorinated? Consider constitutional isomers only, ignore stereoisomers.

Problem

How many monochloro substitution products are produced when the alkanes below are chlorinated? Consider constitutional isomers only, ignore stereoisomers.

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Practice Problems
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