Isomerism Flashcards

1
Q

Define isomer

A

Molecules that have the same molecular formula but the atoms are arranged differnetly

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2
Q

What are the two types of isomers

A

Structural isomerism and stereoisomerism

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3
Q

Define structural isomerism

A

Same molecular formula but different structural formulae

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4
Q

What are the three types of strcutrua; isomerism

A

Functional
Positional
CHain

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5
Q

What is chain isomerism

A

Compounds with the same molecular formula but different
structures of the carbon skeleton

e.g. butan1ol to 2methylpropanol

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6
Q

What is Functional isomerism

A

Compounds with the same molecular formula but with
atoms arranged to give different functional groups

For example:
Ethanol——>methoxymethane

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7
Q

What is positional isomerism

A

The same functional group attatched to the main chain at differnet points

for example1 chloropropane —> 2chloropropane

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8
Q

What is Stereoisomerism

A

The same strutcural formula but differ in arrangements of the bonds

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9
Q

What are the two types of stereoisomerism

A

Optical isomerism
E-Z isomerism

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10
Q

What is E-Z isomerism

A

It tells you abt the positions of the subsitituents at either side of a C=C double bond

E=opposite side

Z= the two subsitituents are on the saem side

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11
Q

Why do E-Z isomers exist

A

Due to restricted rotation about the C=C bond

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12
Q

When do E-Z Isomers arise

A

When there is restricted rotation around the c=c bond
There are two different groups/atoms attached both ends of the double bond

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13
Q

Which group would be the priority group

A

The atom with the bigger atomic number is classed as the priority atom
If the atoms are the same look at the next group

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14
Q

How do E-Z isomerisms differ

A

Different boiling point

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15
Q

Which isomer out of Z and E has the higher boiling point and why

A

Z has the higher boiling point as it is a polar molecule so it has dipole dipole and van der waals whereas in E it only has Van der waals and is non polar

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