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Provide the IUPAC name for the following compound. Provide the IUPAC name for the following compound.

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(2S, 3R)-2...

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Predict the product for the following reaction. Predict the product for the following reaction. A) 2-methyl-1-hexanol B) 2-methoxy-2-methylhexane C) 1-methoxy-2-methylhexane D) 2-methoxy-3-methylhexane E) 2-methyl-2-hexanol


A) 2-methyl-1-hexanol
B) 2-methoxy-2-methylhexane
C) 1-methoxy-2-methylhexane
D) 2-methoxy-3-methylhexane
E) 2-methyl-2-hexanol

F) A) and E)
G) All of the above

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The polyethers that function like crown ethers are called _________.

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Provide the reagents necessary to carry out the following conversion. Provide the reagents necessary to carry out the following conversion.

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Predict the product(s) for the following reaction. Predict the product(s) for the following reaction. A) I B) II C) III D) IV E) none of these Predict the product(s) for the following reaction. A) I B) II C) III D) IV E) none of these


A) I
B) II
C) III
D) IV
E) none of these

F) A) and B)
G) D) and E)

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Provide a stepwise synthesis for the following. Provide a stepwise synthesis for the following.

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Provide a stepwise synthesis for the following. Provide a stepwise synthesis for the following.

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Draw all constitutional isomers with molecular formula C4H8O having an ether functional group.

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Provide the structure for (1S,2R)-1-ethyl-2-methyl-1,2-epoxycyclohexane.

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Predict the product(s) for the following reaction. Predict the product(s) for the following reaction. A) I B) II C) III D) IV E) none of these Predict the product(s) for the following reaction. A) I B) II C) III D) IV E) none of these


A) I
B) II
C) III
D) IV
E) none of these

F) None of the above
G) A) and E)

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Provide an IUPAC name for the following compound. Provide an IUPAC name for the following compound.

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4-t-butyl-...

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A compound with molecular formula C6H14O displays the following IR, 1HNMR and 13CNMR spectra. Propose a structure for this compound. IR: 1200cm-1 A compound with molecular formula C<sub>6</sub>H<sub>14</sub>O displays the following IR, <sup>1</sup>HNMR and <sup>13</sup>CNMR spectra. Propose a structure for this compound. IR: 1200cm<sup>-1</sup> SDBS SDBSA compound with molecular formula C<sub>6</sub>H<sub>14</sub>O displays the following IR, <sup>1</sup>HNMR and <sup>13</sup>CNMR spectra. Propose a structure for this compound. IR: 1200cm<sup>-1</sup> SDBS

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Predict the product for the following reaction. Predict the product for the following reaction. A) 3-methyl-3-pentanol B) 3-ethoxy-3-methylpentane C) 3-methyl-2-pentanol D) 2-ethoxy-3-methylpentane E) 1-ethoxy-3-methylpentane


A) 3-methyl-3-pentanol
B) 3-ethoxy-3-methylpentane
C) 3-methyl-2-pentanol
D) 2-ethoxy-3-methylpentane
E) 1-ethoxy-3-methylpentane

F) A) and B)
G) B) and E)

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Provide a curved arrow mechanism for the formation of the product shown. Provide a curved arrow mechanism for the formation of the product shown.

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blured image_TB4454_00...

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Which one of the following reactions would produce (S) -3-methoxyheptane in high yield?


A) sodium (S) -3-heptoxide + bromomethane
B) sodium (R) -3-heptoxide + bromomethane
C) sodium methoxide + (S) -3-bromoheptane
D) sodium methoxide + (R) -3-bromoheptane

E) A) and B)
F) None of the above

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Provide a stepwise synthesis for the following. Provide a stepwise synthesis for the following.

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Predict the product for the following reaction. Predict the product for the following reaction.

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Provide the structure for (R)-2,2,3-trimethyl-3-phenyloxirane.

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Predict the product(s) for the following reaction. Predict the product(s) for the following reaction. A) I B) II C) III D) IV E) none of these Predict the product(s) for the following reaction. A) I B) II C) III D) IV E) none of these


A) I
B) II
C) III
D) IV
E) none of these

F) C) and D)
G) B) and C)

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Provide the reagents necessary to prepare the following compound using a Williamson ether synthesis reaction. Provide the reagents necessary to prepare the following compound using a Williamson ether synthesis reaction.

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