1 Introduction to Organic Chemistry Flashcards

(16 cards)

1
Q

empirical formula

A

the simplest whole number ratio of atoms of each element in a compound

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2
Q

molecular formula

A

the true number of atoms of each element in a compound

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3
Q

general fornula

A

all members of a homologous series follow this e.g. alkanes CnH2n+2

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4
Q

structural formula

A

shows structural arrangement of atoms within a molecule

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5
Q

displayed formula

A

shows every atom and every bond in an organic compound

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6
Q

skeletal formula

A

shows bonds of any non-carbon atoms

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7
Q

homologous series

A

all follow same general formula and react in similar ways

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8
Q

structural isomerism

A

same molecular formula, different structures

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9
Q

chain isomerism

A

same molecular formula, different carbon chain
e.g. C4H10 CH3CH2CH2CH3 or CH3CH(CH3)2

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10
Q

what happens as branching increases?

A

boiling point decreases as molecule chains can pack less tightly so aren’t as close together

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11
Q

functional group isomerism

A

same molecular, different functional group
alkenes and cycloalkanes
alcohols and ethers
aldehydes and ketones

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12
Q

position isomerism

A

same molecular formula but functional group is in a different position along the chain

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13
Q

stereoisomerism

A

same molecular formula and structural formula but bonds arranged differently in space

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14
Q

why does geometric isomerism occur?

A

both sides of the C=C bond have different groups attached and there is no rotation around the C=C

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15
Q

E-Z isomers

A

E Isomers: on OPPOSITE sides of the bond
Z isomers: on the SAME side of the bond

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16
Q

CIP priority rules

A

The first atom bonded to the carbon which has the HIGHER Ar is given higher priority
e.g. if Br and C bonded to a C=C, Br is given priority
if the same Ar, look to atom bonded to that one