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Which molecule below is an alkene?


A) CH3CH2OCH2CH3
B) (CH3) 2CHCH2OH
C) (CH3) 2C=CH2
D) (CH3) 2CHCH2NH2
E) CH3CH2CH2CO2H

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

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C

Consider 1,2-dibromoethene, shown below. Use arrows to represent the individual bond dipoles. Would you expect this molecule to be polar? Briefly explain your reasoning. Consider 1,2-dibromoethene, shown below. Use arrows to represent the individual bond dipoles. Would you expect this molecule to be polar? Briefly explain your reasoning.

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blured image No, you would not expect this...

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The HNC bond angle in the cation [CH2NH2]+ is approximately ________.


A) 60°
B) 90°
C) 109.5°
D) 120°
E) 180°

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

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Which of the following statements concerning the cyclic molecule shown is not true? Which of the following statements concerning the cyclic molecule shown is not true?   A)  It contains a π molecular orbital formed by the overlap of a carbon p atomic orbital with an oxygen p atomic orbital. B)  It contains a σ molecular orbital formed by the overlap of two carbon sp<sup>2</sup> hybrid atomic orbitals. C)  It contains a σ molecular orbital formed by the overlap of two carbon sp<sup>3</sup> hybrid atomic orbitals. D)  It contains a π molecular orbital formed by the overlap of two carbon p atomic orbitals. E)  It contains a σ molecular orbital formed by the overlap of a carbon p atomic orbital with an oxygen sp<sup>3</sup> atomic orbital.


A) It contains a π molecular orbital formed by the overlap of a carbon p atomic orbital with an oxygen p atomic orbital.
B) It contains a σ molecular orbital formed by the overlap of two carbon sp2 hybrid atomic orbitals.
C) It contains a σ molecular orbital formed by the overlap of two carbon sp3 hybrid atomic orbitals.
D) It contains a π molecular orbital formed by the overlap of two carbon p atomic orbitals.
E) It contains a σ molecular orbital formed by the overlap of a carbon p atomic orbital with an oxygen sp3 atomic orbital.

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

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Choose the correct hybridization for the atom indicated in the molecule below. Choose the correct hybridization for the atom indicated in the molecule below.   A)  sp B)  sp<sup>2</sup> C)  sp<sup>3</sup> D)  none of the above


A) sp
B) sp2
C) sp3
D) none of the above

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

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How many carbon-carbon σ bonds are present in the molecule shown? How many carbon-carbon σ bonds are present in the molecule shown?   A)  1 B)  2 C)  3 D)  4 E)  5


A) 1
B) 2
C) 3
D) 4
E) 5

F) B) and C)
G) A) and C)

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What intermolecular attractions exist in a pure sample of methylthiol, CH3SH?

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London dispersion forces and dipole-dipole attractions.

What kind of molecular orbital (σ, σ*, π, or π*) results when the two atomic orbitals shown below interact in the manner indicated? What kind of molecular orbital (σ, σ<sup>*</sup>, π, or π<sup>*</sup>) results when the two atomic orbitals shown below interact in the manner indicated?

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The hybridization of the nitrogen in the molecule shown below is sp2. Briefly explain why. The hybridization of the nitrogen in the molecule shown below is sp<sup>2</sup>. Briefly explain why.

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This molecule has resonance structures where the lone pair on the nitrogen is delocalized in to the ring through a pi bond. This requires the nitrogen to be sp2 hybridized. 11eab5e1_c953_c1cf_9bae_891643d427ea_TB6199_00

Vildagliptin is a recently released antidiabetic drug (J. Med. Chem. 2010, 7902). Circle and name each functional group in vildagliptin. Vildagliptin is a recently released antidiabetic drug (J. Med. Chem. 2010, 7902). Circle and name each functional group in vildagliptin.

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Choose the correct hybridization for the atom indicated in the molecule below. Choose the correct hybridization for the atom indicated in the molecule below.   A)  sp B)  sp<sup>2</sup> C)  sp<sup>3</sup> D)  none of the above


A) sp
B) sp2
C) sp3
D) none of the above

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

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Use the following structure for the two questions below. Saquinavir Structure Use the following structure for the two questions below. Saquinavir Structure   -Which of the molecules below can be properly called an amine? A)  CH<sub>3</sub>CN B)  CH<sub>3</sub>COOH C)  CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>OH D)  CH<sub>3</sub>CH<sub>2</sub>NHCH<sub>3</sub> E)  CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>NO<sub>2</sub> -Which of the molecules below can be properly called an amine?


A) CH3CN
B) CH3COOH
C) CH3CH2CH2OH
D) CH3CH2NHCH3
E) CH3CH2CH2NO2

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

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From a molecular orbital perspective why isn't there relatively free rotation about the carbon-carbon double bond in ethene (CH2=CH2)?

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Two carbon p atomic orbitals overlap sid...

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Choose the correct hybridization for the atom indicated in the molecule below. Choose the correct hybridization for the atom indicated in the molecule below.   A)  sp B)  sp<sup>2</sup> C)  sp<sup>3</sup> D)  none of the above


A) sp
B) sp2
C) sp3
D) none of the above

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

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Which of the following statements about π molecular orbitals is/are correct?


A) π molecular orbitals are cylindrically symmetric.
B) Most of the electron density in a π molecular orbital is centered above and below the internuclear axis.
C) When two atoms are connected by a double bond, both of these bonds are π bonds.
D) Both statements B and C are correct.
E) Statements A, B, and C are all correct.

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

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Sodium hydride (NaH) is a base that is commonly used in organic reactions. The pKa of H2 is 36. Which of the following compounds could not be used as a solvent if you were using NaH?


A) Sodium hydride (NaH)  is a base that is commonly used in organic reactions. The pKa of H<sub>2</sub> is 36. Which of the following compounds could not be used as a solvent if you were using NaH? A)    B)    C)  CH<sub>3</sub>CH<sub>2</sub>OH D)  CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub>CH<sub>3</sub>
B) Sodium hydride (NaH)  is a base that is commonly used in organic reactions. The pKa of H<sub>2</sub> is 36. Which of the following compounds could not be used as a solvent if you were using NaH? A)    B)    C)  CH<sub>3</sub>CH<sub>2</sub>OH D)  CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub>CH<sub>3</sub>
C) CH3CH2OH
D) CH3CH2CH2CH2CH3CH3

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

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Clonazapam (TM) is used to treat seizures and panic disorders and is shown below. Are there any aromatic hydrocarbons in the molecule? If so, circle them. Clonazapam (TM) is used to treat seizures and panic disorders and is shown below. Are there any aromatic hydrocarbons in the molecule? If so, circle them.

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Yes, there...

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Draw a three-dimensional model of methanol, CH3OH, including lone pairs of electrons using wedges, dashes and straight lines.

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The HCH bond angle in allene (H2CCCH2) is ________.

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An orbital can be described by its ________, which is the mathematical description of the shape of the electron wave as it oscillates.

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