Exam 10: Structure and Synthesis of Alcohols

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In a 1-butanol molecule, what part of the molecule is described as hydrophilic?

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Provide the structure of the major organic product in the reaction shown below. (CH3)2CHCl Provide the structure of the major organic product in the reaction shown below. (CH<sub>3</sub>)<sub>2</sub>CHCl

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Arrange the following alcohols in order of increasing boiling point: (CH3)3COH, CH3(CH2)4OH, (CH3)3CCH2OH, and (CH3)2CHCH2CH2OH.

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Provide the major organic product of the reaction below. Provide the major organic product of the reaction below.

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Provide the major organic product(s) of the reaction below. Provide the major organic product(s) of the reaction below.

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Provide the IUPAC name for the compound below. Provide the IUPAC name for the compound below.

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Ethanol that contains added impurities that make it unfit for drinking is described as ________.

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Provide the structure of the major organic product in the reaction shown below. Provide the structure of the major organic product in the reaction shown below.

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Provide the reagents necessary to carry out the transformation shown below. Provide the reagents necessary to carry out the transformation shown below.

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Provide the structure of the major organic product in the reaction below. Provide the structure of the major organic product in the reaction below.

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Using any compound that contains a carbonyl as your starting material, how would you synthesize butan-2-ol?

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In addition to the use of complex metal hydrides, what other reaction can be used to reduce aldehydes and ketones to alcohols?

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Provide the major organic product of the following reaction. Provide the major organic product of the following reaction.

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Provide the reagents necessary to accomplish the following transformation. Provide the reagents necessary to accomplish the following transformation.

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Provide the name of the major organic product that results when 1-pentene is subjected to hydroboration/oxidation.

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Explain why the compound below is unsuitable as a starting material to form a Grignard reagent. Explain why the compound below is unsuitable as a starting material to form a Grignard reagent.

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