Exam 3 Multipe Choice Flashcards

1
Q

What is the configuration of the asymmetric center in each of the following compounds?

A

R, S, R

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2
Q

What is the relationship between the compounds shown below?

A

Enantiomer

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3
Q

Which are identical compounds?

A

a-c

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4
Q

Which of the following molecules will rotate the plane of polarization of plane-polarized light?

A

1 only

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5
Q

(S)-Mendelic acis has a specific rotation of -158 degrees. What would be the observed specific rotation of (R)-Mendelic acid?

A

+158

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6
Q

Which compound has different stereoisomers?

A

CH3CH(OH)CH2CH(Br)CH3

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7
Q

Which one of these is the most appropriate definition of enatiomers?

A

Non-superimposable molecules that are mirror images of each other

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8
Q

Which of these centers can never be a chirality center as described?

A

An uncharged sp3-o with inly 2 bonds

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9
Q

Which of these when present eliminates the possibility for streoisomerism in molecules?

A

Plane of symmetry

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10
Q

Which one of these is not correct about meso compounds?

A

The stereoisomer must rotate plane polarized light.

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11
Q

Which of the following best describes a racemate or racemic mixture?

A

50-50% mixture of enantiomers

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12
Q

Which of the following structures correspond to (S)-(+)-enantiomer?

A

Structure A

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13
Q

What is the benefit of prescribing a drug as a single enantiomer?

A

A single enantiomer spares the patient from having to metabolize the less potent enantiomer and decreases the chance of unwanted drug interactions.

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14
Q

In 1992 the FDA recommended the use of modern synthesis and separation techniques to produce single enantiomer drugs. Which of the following is not a technique to separate enantiomers?

A

Chiral chromatography

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15
Q

How many chrality centers are there in the structure of penicillamine shown below?

A

1

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