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Stereochemistry Substitution Quiz

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Stereochemistry Substitution Quiz

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Stereochemical basics test

Created by

Chanchal Sharma
Chanchal Sharma
India

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Stereochemistry Substitution Quiz
 

Stereochemistry Substitution QuizOnline version

Stereochemical basics test

by Chanchal Sharma
1

What term describes molecules that rotate plane-polarized light to the right?

2

What is a mirror-image pair of non-superimposable molecules called?

3

Which carbon center characterizes chirality when four different substituents attach to it?

4

What term describes a mixture with equal enantiomer amounts that shows no optical rotation?

5

Which scientists argued that tetrahedral carbon allows non-superimposable mirror images?

6

What is the sign used to denote a compound that rotates plane-polarized light to the left?

7

What property do enantiomers share and differ in?

8

What is the process of converting an enantiomer into a racemic mixture called?

9

Which term refers to objects that are nonsuperimposable on their mirror images, like hands?

10

Which example is a chiral molecule from the text?

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Dextrorotatory molecules rotate light clockwise.

Enantiomers are non-superimposable mirror images.

An asymmetric carbon leads to chirality.

Racemic mixes cancel optical rotation.

Van't Hoff and Le Bel proposed the tetrahedral model.

Laevorotatory rotation is negative.

Enantiomers have identical phys. properties except optical rotation.

Racemisation yields equal enantiomers.

Chirality describes non-superimposable mirror images.

2-bromopropanoic acid is listed as chiral example.

 
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