Introduction to organic chemistry Flashcards

1
Q

hydrocarbon

A

compound consisting of carbon and hydrogen only

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2
Q

saturated

A

contains single carbon bonds only

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3
Q

unsaturated

A

contains a carbon-carbon double bond

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4
Q

molecular formula

A

the formula which shows the actual number of each type of atom

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5
Q

empirical formula

A

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

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6
Q

general formula

A

algebraic formula for a homologous series

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7
Q

structural formula

A

shows the minimal detail that shows the arrangement of atoms in a molecule e.g. for butane CH3CH2CH2CH3

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8
Q

displayed formula

A

shows all the covalent bonds and atoms present in a molecule

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9
Q

skeletal formula

A

shows the simplified organic formula, shown by removing hydrogen atoms from alkyl chains, leaving just a carbon skeleton and associated functional groups

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10
Q

functional group

A

a group of atoms / an atom responsible for the characteristic reactions of a compound

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11
Q

homologous series

A

families of organic compounds with the same functional group and same general formula

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12
Q

characteristics of a homologous series

A

they show a gradual change in physical properties such as MP as molecular mass increases

Each member differs by CH2 from the last

Same chemical properties

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13
Q

functional group of an alkane

A

c-c

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14
Q

functional group of alkenes

A

c(double bond)c

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15
Q

functional group of alcohols

A

C-OH

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16
Q

Prefix and suffix of alchols

A

suffix: -ol
prefix : hydroxy-

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17
Q

functional groups of halogenoalkanes

A

c-halogen

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18
Q

prefix of halogenoalkanes

A

chloro-
bromo-
iodo-

19
Q

functional group of aldehydes

A

on the end of the chain there is a double bond upwards for oxygen and a single bond coming off the carbon for hydrogen

20
Q

prefix of aldehydes

A

-al

21
Q

suffix of aldehydes

A

formyl-

22
Q

functional group of ketones

A

in the middle of the chain there is a double bond upwards coming off a carbon atom for oxygen

23
Q

suffix of ketones

A

-one

24
Q

prefix of ketones

A

oxo-

25
Q

functional group of carboxylic acids

A

at the end of the chain there is a double bond upwards coming off the carbon for oxygen and a single bond coming off the carbon for OH

26
Q

suffix of carboxylic acids

A

-oic acids

27
Q

functional group of esters

A

in the middle of the chain there is a double bond coming off the carbon for oxygen and also a single bond coming off the carbon for oxygen

28
Q

order of priority for all homologous series (highest first)

A

carboxylic acids
Aldehydes
Ketones
Alcohols
Alkenes
Halogenoalkanes

29
Q

IUPAC rules for nomenclature

A
  1. Count the number of carbon atoms in the longest continuous unbranched carbon chain for the stem of the name
  2. Identify any branches or functional groups
  3. Number the carbon atoms in the longest chain to indicate positions of branches or functional groups. If there are more than 1 functional groups, put it in alphabetical order
  4. If the same groups appear more than once, indicate how many times they are present
30
Q

how do you determine which functional group gets the suffix/prefix

A

the functional group with the highest priority gets the suffix ending

31
Q

structural isomers

A

same molecular formula different structural formula

32
Q

chain isomers

A

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

33
Q

position isomers

A

compounds with the same molecular formula but different structures due to different positions of the same functional group on the same carbon skeleton

34
Q

functional group isomers

A

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

35
Q

why is cyclobutane not an alkene even though it follows the general formula of alkenes

A

it does have the general formula CnH2n but it is not an alkene because it does not contain a carbon-carbon double bond

36
Q

aliphatic compounds

A

a compound containing carbon and hydrogen joined together in straight chains, branched chains, or non-aromatic chains

37
Q

alicylic compounds

A

an aliphatic compound which contains atoms arranged in non-aromatic rings, with or without side chains

38
Q

aromatic compounds

A

a compound containing a benzene ring

39
Q

formula of benzene

A

C6H6

40
Q

steroisomers

A

same structural formula but different spatial arrangement of atoms

41
Q

why do E-Z isomers exist

A

due to the restricted rotation about the carbon-carbon double bond (single carbon-carbon covalent bonds can easily rotate)

There are two different groups/atoms attached to both ends of the double bond

42
Q

which type of isomerism do alkenes exhibit

A

E-Z steroisomerism

43
Q

CIP priority rules

A
  1. The atom of higher atomic number which is attached to each side of the double bond, is given priority
  2. If the atoms are the same, consider the atoms at distance from the double bond. The group containing the atom of higher atomic number is given priority
44
Q
A