Study Set Content:
101- Flashcard

. However, if a single enantiomer is examined (all sample molecules being right-handed, or all being left-handed), the plane of polarization is rotated in either a (), and the analyzer must be turned an appropriate matching angle

clockwise (positive) or counter-clockwise (negative) direction

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102- Flashcard

analyzer must be turned an appropriate matching angle, α, if full light intensity is to reach the

detector

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103- Flashcard

One enantiomer will rotate polarized light in a clockwise direction, termed

dextrorotatory or (+),

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104- Flashcard

and its mirror-image partner in a counter-clockwise manner, termed

levorotatory or (–).

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105- Flashcard

• If equal quantities of each enantiomer are examined , using the same sample cell, then the magnitude of the rotations will be the same, with one being positive and the other

negative

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106- Flashcard

To be absolutely certain whether an observed rotation is positive or negative it is often necessary to make a () using a different amount or concentration of the sample.

second measurement

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107- Flashcard

Since it is not always possible to obtain or use samples of exactly the same size, the observed rotation is usually corrected to compensate for variations in sample quantity and cell length. Thus it is common practice to convert the observed rotation, αα, to a specific rotation, by the following formula

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108- Flashcard

is the specific rotation

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109- Flashcard

is the length in dm

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110- Flashcard

is the concentration in g/ml

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111- Flashcard

designates that the light used is the 589 line from a sodium lamp

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112- Flashcard

Compounds that rotate the plane of polarized light are termed

optically active.

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113- Flashcard

Each enantiomer of a stereoisomeric pair is optically active and has an equal but() specific rotation

opposite-in-sign

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114- Flashcard

BIOT law

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115- Flashcard

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116- Flashcard

c

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117- Flashcard

l

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118- Flashcard

D

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119- Flashcard

T

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120- Flashcard

– a physical process where the components (solutes) of a sample mixture are separated as a result of their differential distribution between stationary and mobile phases.

Chromatography

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