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

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Identify the product for the reaction. Identify the product for the reaction. A) B) CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH C) D) CH<sub>3</sub>CH<sub>2</sub>OH E)


A) Identify the product for the reaction. A) B) CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH C) D) CH<sub>3</sub>CH<sub>2</sub>OH E)
B) CH3CH2CH2OH
C) Identify the product for the reaction. A) B) CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH C) D) CH<sub>3</sub>CH<sub>2</sub>OH E)
D) CH3CH2OH
E) Identify the product for the reaction. A) B) CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH C) D) CH<sub>3</sub>CH<sub>2</sub>OH E)

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Provide the structure of the cyanohydrin that results when cyclopentanone reacts with HCN.

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Give the product for the following reaction. Give the product for the following reaction. A) B) C) D) E)


A) Give the product for the following reaction. A) B) C) D) E)
B) Give the product for the following reaction. A) B) C) D) E)
C) Give the product for the following reaction. A) B) C) D) E)
D) Give the product for the following reaction. A) B) C) D) E)
E) Give the product for the following reaction. A) B) C) D) E)

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Which of the following is least reactive towards Grignard's reagent PhMgBr? Which of the following is least reactive towards Grignard's reagent PhMgBr? A) I B) II C) III D) IV E) V


A) I
B) II
C) III
D) IV
E) V

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Give the best name for the structure. Give the best name for the structure. A) 1-oxo-2-butanone B) 1,3-dioxobutane C) 3-oxobutanal D) 3-oxobutanol E) 1-oxo-2-propanone


A) 1-oxo-2-butanone
B) 1,3-dioxobutane
C) 3-oxobutanal
D) 3-oxobutanol
E) 1-oxo-2-propanone

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

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3-ethyl-4-...

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An unknown compound (A),C10H12O,gave the following proton NMR data: (a)triplet,at 1.0 ppm (3H) (b)quartet,at 2.4 ppm (2H) (c)singlet,at 3.7 ppm (2H) (d)multiplet,at 7.2 ppm (5H) Propose a structure for (A).

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Which of the following is cyclohexanone? Which of the following is cyclohexanone? A) I B) II C) III D) IV E) V


A) I
B) II
C) III
D) IV
E) V

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Provide the structure of the imine that results when 4-heptanone is treated with CH3CH2CH2NH2 in the presence of an acid catalyst.

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Which of the following is the best method for preparing lactic acid from acetaldehyde? Which of the following is the best method for preparing lactic acid from acetaldehyde? A) Cl<sub>2</sub>; <sup>-</sup>OH; CH<sub>3</sub>OH B) CH<sub>3</sub>MgBr; <sup>-</sup>OH C) KMnO<sub>4</sub>; <sup>-</sup>OH D) HC N; H<sub>3</sub>O<sup>+</sup>/heat E) Cl<sub>2</sub>; Mg/ether; <sup>-</sup>OH


A) Cl2; -OH; CH3OH
B) CH3MgBr; -OH
C) KMnO4; -OH
D) HC Which of the following is the best method for preparing lactic acid from acetaldehyde? A) Cl<sub>2</sub>; <sup>-</sup>OH; CH<sub>3</sub>OH B) CH<sub>3</sub>MgBr; <sup>-</sup>OH C) KMnO<sub>4</sub>; <sup>-</sup>OH D) HC N; H<sub>3</sub>O<sup>+</sup>/heat E) Cl<sub>2</sub>; Mg/ether; <sup>-</sup>OH N; H3O+/heat
E) Cl2; Mg/ether; -OH

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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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Which enantiomer is formed from attack of a methyl Grignard reagent on the si face of benzaldehyde? Which enantiomer is formed from attack of a methyl Grignard reagent on the si face of benzaldehyde? A) I B) II C) III D) IV E) V


A) I
B) II
C) III
D) IV
E) V

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Give the products for the following reaction. Give the products for the following reaction.

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Provide the structure of cyclohexanone oxime.

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Provide the proper IUPAC name for CH3CHOHCH2COCH2C(CH3)2CH2CH3.

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2-hydroxy-...

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What are the products of the following hydrolysis? What are the products of the following hydrolysis?

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What reagent can be used to convert benzophenone into triphenylmethanol?

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PhMgBr fol...

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By which single-step process can benzene be readily converted into acetophenone?

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CH3COCl,AlC...

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Provide the proper IUPAC name for PhCH2CH(CH3)CH2CH2CHO.

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4-methyl-5...

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