13.2 Steroisomerism Flashcards

1
Q

What are two types of stereoisomerism

A

E/Z isomerism

Optical isomerism

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2
Q

When can E/Z isomerism occur

A

Only in compounds with a C=C double bond

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3
Q

When can optical isomerism occur

A

In a wider range of compounds including alkanes with no functional groups

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4
Q

When does Stereoisomerism around double bonds arise

A

Because rotation about the double bond is restricted and the groups attached to each carbon atom are therefore fixed relative to each other
The rigidity is caused by the position of the π-bond’s electron density above and below the plane of the σ-bond

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5
Q

What are the conditions a molecule must satisfy in order to have E/Z isomerism

A

A C=C double bond

Different groups attached to each carbon atom of the double bond

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6
Q

Which of but-1-ene and but-2-ene can have E/Z isomers

A

but-2-ene

Because it has a methyl group AND a hydrogen atom on each of the carbon atoms of the double bond

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7
Q

What is Cis-trans isomerism

A

The name commonly used to describe a special case of E/Z isomerism
One of the attached groups on each carbon atom of double bond must be hydrogen

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8
Q

Difference between a cis isomer and a trans isomer

A

Cis - hydrogen atoms on each carbon in double bond on SAME side of the molecule
Trans - hydrogen atoms are diagonally OPPOSITE each other

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9
Q

In cis-trans isomerism

A

The cis isomer is the Z isomer

The trans isomer is the E isomer

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10
Q

What are the Cahn-Ingold-Prelog rules of isomerism

A

Atoms attached to each carbon atom in double bond are given priority based upon their atomic number
If groups of higher priority on same side of double bond, compound is Z isomer
If groups of higher priority are diagonally placed across double bond, compound is E isomer

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11
Q

How does priority change as atomic number increases

A

Higher number, higher priority

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