MEDCHEM.1 Introduction to chirality Flashcards

1
Q

What are structural isomers

A

Structural isomers have the same molecular formula but differ in the arrangement of atoms within the molecule.

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2
Q

What are stereoisomers

A

Stereoisomers have the same molecular formula and the same connectivity of atoms, but differ in their spatial arrangement.

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3
Q

Define chirality

A

The property of an object or molecule that is not superimposable on its mirror image.

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4
Q

Define chiral

A

A molecule is chiral if it cannot be superimposed onto its mirror image.

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5
Q

Define achiral

A

A molecule is achiral if it can be superimposed onto its mirror image.

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6
Q

Define stereogenic center

A

A stereogenic center, also known as a chiral center, is a carbon atom that is bonded to four different groups. It is responsible for generating stereoisomers.

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7
Q

Define enantiomers

A

A pair of molecules that are non-superimposable mirror images of each other. They have the same connectivity of atoms but differ in their three-dimensional arrangement. Enantiomers are chiral molecules.

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8
Q

Physical properties of enantiomers

A

Enantiomers have identical physical properties such as melting point, boiling point, and density.

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9
Q

Discuss the optical activity of enantiomers

A

Enantiomers exhibit optical activity, which means they rotate the plane of polarized light in opposite directions. One clockwise while the other anticlockwise.

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10
Q

What do you call an enantiomer that causes a clockwise (+) rotation of plane of polarized light?

A

dextrorotatory

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11
Q

What do you call an enantiomer that causes an anticlockwise (-) rotation of plane of polarized light?

A

levorotatory

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12
Q

Name the instrument that allows the differentiation between a pair of enantiomers

A

Polarimeter

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13
Q

How can you differentiate between a pair of enantiomers.

A

By comparing the direction and angle of rotation of polarized light.

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14
Q

What is specific rotation?

A

A measure of the extent and direction of optical rotation caused by a substance.

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15
Q

What is the equation to calculate specific rotation?

A

[α] = α / (c × l)

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16
Q

Define racemic mixture

A

A 50:50 mixture of two enantiomers.

17
Q

Does a racemic mixture exhibit optical activity? Why or why not

A

In a racemic mixture, the enantiomers are present in equal amounts, and their optical rotations cancel each other out. As a result, a racemic mixture exhibits no net optical rotation and is optically inactive.