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What are the units of absorbance, A, in ultraviolet-visible spectroscopy?


A) J.mol-1
B) nm.mol-1
C) J.mol-1.M-1
D) none, A is a dimensionless quantity

E) C) and D)
F) B) and C)

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Which of the following reaction coordinate diagrams explains the formation of different thermodynamic (T) and kinetic products from the same reactants (R) ? Which of the following reaction coordinate diagrams explains the formation of different thermodynamic (T)  and kinetic products from the same reactants (R) ?   A) 1 B) 2 C) 3 D) 4


A) 1
B) 2
C) 3
D) 4

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

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Consider the reaction below to answer the following question(s) : Consider the reaction below to answer the following question(s) :   Enter the appropriate letter in the blank for each the following statements. -The electrophile in this reaction is ____. A) A B) B C) C D) D Enter the appropriate letter in the blank for each the following statements. -The electrophile in this reaction is ____.


A) A
B) B
C) C
D) D

E) All of the above
F) C) and D)

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Consider the following structure. Consider the following structure.   This substance could be produced by the reaction of the following diene and dienophile.  This substance could be produced by the reaction of the following diene and dienophile. Consider the following structure.   This substance could be produced by the reaction of the following diene and dienophile.

A) True
B) False

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Draw two resonance structures of the reactive intermediate that accounts for the formation of 1,2- and 1,4-addition products upon reaction of 1,3-butadiene with one equivalent of bromine.

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What quantity is abbreviated as ε\varepsilon in ultraviolet-visible spectroscopy?


A) absorbance
B) molecular absorptivity
C) intensity of transmitted light
D) wavelength of maximum absorbance

E) A) and B)
F) C) and D)

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What is the correct order of exothermicity for hydrogenation of the following hexadienes upon treatment with H2/Pd (more exothermic > less exothermic) ? What is the correct order of exothermicity for hydrogenation of the following hexadienes upon treatment with H<sub>2</sub>/Pd (more exothermic > less exothermic) ?   A) 1 > 2 > 3 B) 3 > 1 > 2 C) 2 > 1 > 3 D) 3 > 2 > 1


A) 1 > 2 > 3
B) 3 > 1 > 2
C) 2 > 1 > 3
D) 3 > 2 > 1

E) B) and C)
F) A) and B)

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Which of the following laws relates absorbance to the concentration of a sample and the pathlength in ultraviolet-visible spectroscopy?


A) Buzz-Beer law
B) Beer-Lambert law
C) Duff-Beer law
D) Christopher-Lambert law

E) None of the above
F) C) and D)

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The following compound could act as a diene in a Diels-Alder reaction. The following compound could act as a diene in a Diels-Alder reaction.

A) True
B) False

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What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?

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(E)-2,3-di...

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What are the two major organic products obtained from the following reaction? What are the two major organic products obtained from the following reaction?

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When an organic molecule is irradiated with ultraviolet radiation, the energy absorbed by the molecule corresponds to the amount necessary to excite electrons from one molecular orbital to another.

A) True
B) False

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Which of 1,3-cyclohexadiene and 1,4-cyclohexadiene has the greatest heat of hydrogenation (i.e., the most exothermic reaction with H2 in the presence of a catalyst). Provide a brief explanation for your choice ?

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1,4-Cyclohexadiene has a great...

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Which of the following electronic transitions is (are) apparent in the ultraviolet-visible spectrum of acrolein, H2C=CHCHO? 1) n \rarr π\pi * 2) π\pi \rarr π\pi * 3) σ\sigma\rarr π\pi *


A) only 1
B) only 2
C) only 1 and 2
D) 1, 2 and 3

E) None of the above
F) All of the above

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Which of the following is(are) formed upon addition of 1 mol of Br2 to 1,3-cyclohexane? Which of the following is(are)  formed upon addition of 1 mol of Br<sub>2</sub> to 1,3-cyclohexane?   A) only 2 B) only 1 and 3 C) only 2 and 4 D) 1, 2 and 3


A) only 2
B) only 1 and 3
C) only 2 and 4
D) 1, 2 and 3

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

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The following two compounds could be easily distinguished by NMR, IR, UV or MS spectra. The following two compounds could be easily distinguished by NMR, IR, UV or MS spectra.

A) True
B) False

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Provide the structures of the constitutional isomers of the two major organic products obtained from the following reaction? Provide the structures of the constitutional isomers of the two major organic products obtained from the following reaction?

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Which of the following energy diagrams represents the electronic state of the ground state of 1,3-butadiene? Which of the following energy diagrams represents the electronic state of the ground state of 1,3-butadiene?   A) 1 B) 2 C) 3 D) 4


A) 1
B) 2
C) 3
D) 4

E) A) and C)
F) B) and D)

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What is the systematic IUPAC name of the following compound? What is the systematic IUPAC name of the following compound?   A) (3S,4E) -3-ethyl-3,4-dimethyl-1,4-hexadiene B) (3R,4E) -3-ethyl-3,4-dimethyl-1,4-hexadiene C) (3S,4Z) -3-ethyl-3,4-dimethyl-1,4-hexadiene D) (3R,4Z) -3-ethyl-3,4-dimethyl-1,4-hexadiene


A) (3S,4E) -3-ethyl-3,4-dimethyl-1,4-hexadiene
B) (3R,4E) -3-ethyl-3,4-dimethyl-1,4-hexadiene
C) (3S,4Z) -3-ethyl-3,4-dimethyl-1,4-hexadiene
D) (3R,4Z) -3-ethyl-3,4-dimethyl-1,4-hexadiene

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

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Draw two resonance structures of the reactive intermediate that accounts for the formation of 1,2- and 1,4-addition products upon reaction of 1,3-butadiene with one equivalent of HBr.

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