A) 3
B) 4
C) 5
D) 6
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Multiple Choice
A) CH3CH2CH2CO2H
B)
C) CH3CH2NH2
D)
E)
Correct Answer
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Multiple Choice
A) C10H22
B) C11H22
C) C12H22
D) C5H10
E) C5H8
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Multiple Choice
A) 1-butyne
B) cycloheptene
C) 3-methylheptane
D) 2-heptyne
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Multiple Choice
A) CH3-CH2-CH3
B) CH3-CH2-CHBr-CH3
C) CH3-CHCl-CH3
D) CH3-CH2-CH2Br
E) CH3-CH2-CBr2-CH3
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Multiple Choice
A) S configuration
B) R configuration
C) E configuration
D) Z configuration
E) d configuration
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Multiple Choice
A) Stereoisomers differ in the way atoms are connected but have identical spatial orientation of atoms. They can be conformational or configurational.
B) Stereoisomers differ in the way atoms are connected but have identical spatial orientation of atoms. They can be constitutional or configurational.
C) Stereoisomers have the same atom connectivity but have different spatial orientation of atoms. They can be constitutional or enantiomeric.
D) Stereoisomers have the same atom connectivity but have different spatial orientation of atoms. They can be conformational or configurational.
E) Stereoisomers have the same atom connectivity but have different functional groups on the same positions of the carbon backbone. They can be conformational or configurational.
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Essay
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Multiple Choice
A) Infrared absorption spectroscopy is a common method for identifying functional groups in the structure of organic molecules.
B) Infrared absorption spectroscopy is a technique that makes use of the fact that infrared photons can excite the valence electrons in organic molecules.
C) Infrared absorption spectroscopy is a simple yet powerful method for determining the absolute configuration of chiral organic molecules.
D) Infrared absorption spectroscopy observes the energy emitted by vibrating bonds in molecules.
E) Infrared absorption spectroscopy is a technique frequently used in separation of isomers.
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Multiple Choice
A) (CH3CH2) 2NH
B) CH3CH2CH2CH2CO2CH3
C) CH3CH2CH2CH2-O-CH2CH2CH3
D) CH3CH=O
E) CH3COCH3
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Multiple Choice
A) esters, ethers, carboxylic acids
B) esters, carboxylic acids, amines
C) esters, carboxylic acids, amides
D) esters, alcohols, amines
E) ethers, amides, esters
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Multiple Choice
A) Angle strain is the angle between carbon bonds on the outer side of a cycloalkane ring.
B) Angle strain is the difference between an ideal bond angle for sp3 hybridized carbon atoms and the actual bond angle in the ring.
C) Angle strain is the difference between and ideal bond angle for sp hybridized carbon atoms and the actual bond angle in the ring.
D) Angle strain is the angle between C-C bonds in the cycloalkane ring.
E) Angle strain is the difference between the C-C bond angles found in a flat ring structure and in an actual ring structure
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Multiple Choice
A)
B)
C)
D)
E)
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Essay
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Multiple Choice
A) butane
B) butanoic acid
C) cyclohexane
D) ethanol
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Multiple Choice
A) -NH2, -C(=O) H, -COOH, -CH3
B) -CH3, -COOH, -C(=O) H, -NH2
C) -NH2, -CH3, -C(=O) H, -COOH
D) -NH2, -COOH, -C(=O) H, -CH3
E) -NH2, -CH3, -COOH, -C(=O) H
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Multiple Choice
A) 1
B) 2
C) 3
D) 4
E) 5
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Essay
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Multiple Choice
A)
B)
C)
D)
E)
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Multiple Choice
A) Organic halides have one or more H atoms substituted by an electronegative atom from group 16 of the periodic table.
B) Organic halides have one or more C atoms substituted by an electronegative atom from group 17 of the periodic table.
C) Organic halides have one or more H atoms substituted by an electronegative atom from group 17 of the periodic table.
D) Organic halides have one or more H atoms substituted by an electropositive atom from group 17 of the periodic table.
E) Organic halides have one or more H atoms substituted by an electronegative atom from group 7 of the periodic table.
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