isomerism Flashcards

(32 cards)

1
Q

what are the two types of isomers

A

structural isomers and stereoisomers

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2
Q

define structural isomers

A

isomers with the same molecular formula but a different structural arrangement of atoms

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3
Q

define steroisomers

A

isomers with the same molecular formula but a different spatial arrangement of atoms

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4
Q

what are the three types of structural isomers

A

chain isomers, positional isomers and functional group isomers

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5
Q

define chain isomers

A

isomers with a different structural arrangement of the carbon backbone

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6
Q

chain isomers have similar _________ properties but different ________ properties

A

chemical, physical

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7
Q

what gives them similar chemical properties

A

they have the same functional group

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8
Q

what gives them different physical properties

A

they have different shapes, for example branched alkane cant pack closely together so they have lower boiling points but straight can

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9
Q

draw the two chain isomers butane and 2-methylpropane

A
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10
Q

define positional isomers

A

isomers with the same functional group but the functional group is bonded to a different carbon on the carbon chain

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11
Q

position isomers have different _________ properties and different ________ properties

A

chemical, physical

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12
Q

what gives them different chemical properties

A

although they have the same functional group, the position of it affects reactivity. Think about the oxidation of a primary vs secondary alcohol

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13
Q

what gives them different physical properties

A

they are different shapes, changing how molecules pack

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14
Q

draw the two positional isomers propan-1-ol and propan-2-ol

A
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15
Q

define functional group isomers

A

isomers with different functional groups

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16
Q

functional group isomers have different _________ properties and different ________ properties

A

chemical, physical

the reasons are obvious

17
Q

what causes stereoisomerism in alkenes

A

the restricted rotation around the C=C bond

18
Q

is rotation restricted in a C-C bond

A

no, they can rotate freely

19
Q

what is needed for E/Z isomerism to occur

A

when each carbon in the C=C bond has two or more different groups bonded to it

20
Q

Draw the E and Z isomers of but-2-ene

21
Q

where are the hydrogen atoms in E-but-2-ene

A

hydrogen atoms are on opposite sides

22
Q

where are the hydrogen atoms in Z-but-2-ene

A

hydrogen atoms are on the same side

23
Q

Draw the E and Z isomers of haloethene

24
Q

where are the heavier atoms in E-haloethene

A

heavier atoms are on opposite sides

25
where are the heavier atoms in Z-haloethene
heavier atoms are on the same side
26
what is needed for cis/trans isomerism to occur
when each carbon in the C=C bond has one hydrogen atom bonded to it
27
Draw the trans and cis isomers of but-2-ene and the skeletal formula
28
where are the hydrogen atoms on trans-but-2-ene
they are on opposite sides
29
where are the hydrogen atoms on cis-but-2-ene
they are on the same side
30
whats a disadvantage of using cis trans nomenclature to name isomers
it cant be used for halothene because each carbon atom in the C=C bond must have one hydrogen atom attached to it, haloethene doesnt.
31
E isomers are the equivalent to...
trans isomers
32
Z isomers are the equivalent to...
cis isomers