Exam 8: Haloalkanes, Halogenation, and Radical Reactions

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Provide the IUPAC name of the following compound. Provide the IUPAC name of the following compound.

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What is the structure of the key intermediate in the following reaction? What is the structure of the key intermediate in the following reaction?

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What is the characteristic of a radical chain termination step?

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Which of the following statements is not true regarding the halogenation of alkanes upon treatment with halogen and light?

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Which of the following accounts for the anti-Markovnikov regiochemistry of the reaction of an alkene with HBr in the presence of peroxides?

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What is the major organic product obtained from the following reaction? What is the major organic product obtained from the following reaction?

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What is the major organic product obtained from the following reaction? What is the major organic product obtained from the following reaction?

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Which of the following has the list of compounds in the correct order of decreasing density (higher density > lower density)?

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What is the major organic product obtained from the following reaction? What is the major organic product obtained from the following reaction?

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Provide the IUPAC name of the following compound (shown as a Fischer projection). Provide the IUPAC name of the following compound (shown as a Fischer projection).

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What is the major organic product obtained from the following reaction? What is the major organic product obtained from the following reaction?

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Which of the following has the list of compounds in the correct order of decreasing molecular polar (more polar > less polar)?

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What type of reactive intermediate is formed in the reaction of propene with N-bromosuccinimide to give 3-bromo-1-propene?

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Which of the following has the list of compounds in the correct order of decreasing polarity (more polar > less polar)?

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What is the major organic product obtained from the following reaction? What is the major organic product obtained from the following reaction?

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What is the major product of autooxidation of cyclohexene? What is the major product of autooxidation of cyclohexene?

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What is the structure of all of the monobrominated products, including regioismers and stereoisomers, obtained from the following reaction? What is the structure of all of the monobrominated products, including regioismers and stereoisomers, obtained from the following reaction?

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Which of the following statements is not true?

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