4.4 Isomerism Flashcards

1
Q

what do hydrocarbons consist of?

A

Hydrogen and carbon

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2
Q

what does the alkane group form?

A

They form a homologous series of hydrocarbons in which the carbon atoms are joined to each other by a single covalent bond

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3
Q

what does a structural formula show?

A

a structural formula shows the number and type of each atom in a molecule

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4
Q

what does a displayed formula show?

A

a displayed formula shows all the bonds clearly as straight lines

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5
Q

when does structural isomerism occur?

A

structural isomerism occurs when two or more compounds have the same molecular formula but different structures

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6
Q

what are chain isomers?

A

chain isomers are structural isomers in which carbon atoms are joined together in different arrangements, such as branches

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7
Q

What are positional isomers?

A

Positional isomers occur when compounds have the same molecular formula and functional group, but the functional group is on different parts of the same carbon chain

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8
Q

what are haloalkanes?

A

haloalkanes are alkanes in which at least one hydrogen is replaced by a halogen atom

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9
Q

how are compounds named when they contain different halogen atoms?

A

they are named in alphabetical order

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10
Q

what are stereoisomers?

A

stereoisomers have the same molecular formula and the same structural formula, but the atoms are arranged differently in space

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11
Q

why are stereoisomers able to exist in alkenes?

A

due to the restricted rotation around the C=C bond

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12
Q

what are the two conditions that must be met for there to be an E-Z isomer?

A
  • the molecule must have a C=C bond

- both C atoms must have two different groups attached to them

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13
Q

when does optical isomerism occur?

A

optical isomerism occurs when a compound contains a carbon atom with four different atoms or groups joined to it

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14
Q

what do we call the carbon with four different groups attached to it?

A

the chiral carbon

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15
Q

what does the presence of optical isomerism mean?

A

that the compound can have two optical isomers, called enantiomers

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16
Q

what is used to show optical activity?

A

a polarimeter

17
Q

what does a polaroid filter do?

A

it only lets rays that vibrate in a particular plane to pass through

18
Q

what do we call the light that passes through a polaroid filter?

A

plane-polarised light

19
Q

how do optical isomers affect the plane of polarisation?

A

optical isomers rotate the plane

20
Q

what is a racemic mixture, or a racemate?

A

a mixture that contains equal amounts of each enantiomer

21
Q

why does a racemate not show optical activity?

A

due to the opposite rotating effects of each enantiomer cancelling each other out

22
Q

why is a racemate formed?

A

due to a molecule being planar, so the carbon can be attacked from above or below with equal probability

23
Q

why is only one enantiomer produced when a compound is synthesised by living organisms?

A

only one enantiomer reactant can bind to an enzyme’s active site

24
Q

how can some enantiomers be distinguished?

A

by their taste or smell

25
Q

what can the enantiomers of medical drugs be the difference between?

A

a toxic substance and one with beneficial effects, such as thalidomide