Isomerism Flashcards

1
Q

two compounds can have the same molecular formula but different……, making them………..

A

structural formulae, making them structural isomers

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2
Q

the two types of structural isomerism are

A

chain isomerism and position isomerism

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3
Q

chain isomerism refers to molecules with

A

different carbon chains

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4
Q

butane and methylpropane are examples of what kind of isomerism

A

chain isomerism

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5
Q

butane and methylpropane are chain isomers because

A

their carbon chains are different

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6
Q

position isomerism refers to molecules with

A

the same functional group attached in different positions on the same carbon chain

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7
Q

propan-1-ol and propan-2-ol are examples of what kind of isomerism

A

position isomerism

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8
Q

true or false: two molecules can be both chain and position isomers?

A

true

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9
Q

in organic chemistry, we use ‘stereo’ to mean

A

the different ways to arrange atoms or groups of atoms

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10
Q

stereoisomers have the same….. and same……. but different……..

A

molecular formula and structural formula, but different arrangements

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11
Q

when showing stereoisomers, we have to (specific way of drawing bonds)

A

draw the bonds at 120 degree angles around the carbon atoms in question, having two groups of atoms or atoms bonded on each carbon of the double C=C

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12
Q

by drawing the bonds at 120 degree angles in stereoisomers, we can see……and…….notation

A

trans- (opposite) and cis- (same side)

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13
Q

trans means

A

the same groups of atoms or single atoms are on opposite sides of the C=C bond and opposite sides of the molecule

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14
Q

cis means

A

the same groups of atoms or single atoms are still on opposite side of the C=C bond, but on the same side of the molecule

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15
Q

compounds which require cis- and trans- to name them are called

A

geometric isomers

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16
Q

geometric isomerism is a kind of

A

stereoisomerism

17
Q

geometric isomerism exists in…..but not……

A

alkenes but not alkanes

18
Q

geometric isomerism cannot occur in alkanes as

A

there is no double bond which stops groups attached to the double C=C bond from rotating

19
Q

what causes geometric isomerism?

A

the double C=C bond in alkenes prevent groups attached to the carbons in the double C=C from rotating, so restricted rotation is created

20
Q

the three steps for E-Z notation are

A

1) Use the part of the name that can be used for both isomers using normal nomenclature
2) Use priority rules to decide which of the two atoms or groups of atoms on each side will be used to compare with the other side. Use the atomic number of the atoms to decide, the highest atomic number is used
3) Now decide whether the highest priority atoms are on the same side (Z) or opposite (E) sides of the molecule