Topic 4- Core organic chemistry Flashcards

1
Q

hydrocarbon

A

compound containing hydrogen and carbon only

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2
Q

saturated hydrocarbon

A

hydrocarbon with single bonds only

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3
Q

unsaturated hydrocarbon

A

hydrocarbon that contains one or more double bonds

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4
Q

homologous series

A

family of compounds with similar chemical properties whose successive members differ by the addition of a -CH2- group

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5
Q

functional group

A

part of the organic molecule that is largely responsible for the molecules chemical properties

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6
Q

aliphatic

A

carbon atoms are joined to each other in unbranched or branched chains or non-aromatic rings

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7
Q

alicyclic

A

carbon atoms are joined to each other in ring structures, with or without branches

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8
Q

aromatic

A

some or all of the carbon atoms are found in a benzene ring

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9
Q

alkanes

A

contain single carbon-carbon bonds

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10
Q

alkenes

A

contain at least one double carbon-carbon bond

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11
Q

alkynes

A

contain at least one triple carbon-carbon bond

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12
Q

alkyl groups

A

side chains

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13
Q

molecular formula

A

number and type of atoms of each element present in a molecule

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14
Q

general formula

A

simplest algebraic formula for any member of a homologous series

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15
Q

displayed formula

A

shows the relative positioning of all of the atoms in a molecule and the bonds between them

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16
Q

structural formula

A

uses the smallest amount of detail necessary to show the arrangement of the atoms in a molecule

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17
Q

skeletal formula

A

simplified organic formula only represented by lines

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18
Q

structural isomers

A

compounds with the same molecular formula but different structural formula

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19
Q

homolytic fission

A

the breaking of a covalent bond with one of the bonded electrons going to each atom, forming two radicals

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20
Q

heterolytic fission

A

the breaking of a covalent bond forming a positive and negative ion

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21
Q

curly arrows

A

show the movement of electron pairs

22
Q

addition reaction

A

two reactants join to form one product

23
Q

substitution reaction

A

an atom or group of atoms is replaced with a different atom or group of atoms

24
Q

elimination reaction

A

removal of a small molecule from a larger one

25
Q

sigma bond

A

the result of the overlap of two orbitals, one from each bonding atom

26
Q

effect of greater chain length

A

more surface points of contact
stronger London forces
requires more energy to break bonds

27
Q

effect of more branching

A

less surface points of contact
weaker London forces
requires less energy to break bonds

28
Q

stages of radical substitution

A

initiation, propagation, termination

29
Q

pi bond

A

sideways overlap of two p orbitals preventing them from rotating around the double bond

30
Q

stereoisomers

A

same structural formula but different arrangement in space

31
Q

E isomers

A

highest priority groups diagonally placed across the double bond

32
Q

Z isomers

A

highest priority groups on the same side of the double bond

33
Q

cis isomers

A

hydrogen atoms and methyl group on each carbon in the double bond on the same side

34
Q

trans isomers

A

hydrogen atoms and methyl groups diagonally opposite each other

35
Q

hydrogenation of alkenes

A

alkene mixed with hydrogen to make an alkane

36
Q

halogenation of alkenes

A

alkenes mixed with a halogen to make a haloalkane

37
Q

hydration of alkenes

A

alkene add water to make an alcohol

37
Q

electrophile

A

electron pair acceptor

38
Q

carbocation

A

an ion that contains a positively charged carbon

39
Q

primary alcohol

A

an alcohol in which the -OH is attached to a carbon atom with either two or 3 hydrogen atoms

40
Q

secondary alcohol

A

an alcohol in which the -OH is attached to a carbon atom that is attached to two carbon chains and a hydrogen atom

41
Q

tertiary alcohol

A

an alcohol in which the -OH is attached to a carbon atom that is attached to three carbon atoms and no hydrogen atoms

42
Q

preparing an aldehyde

A

distillation of a primary alcohol with an oxidising agent and acidified potassium dichromate to make an aldehyde and water

43
Q

preparing a carboxylic acid

A

primary alcohol heated under reflux with an oxidising agent and acidified potassium dichromate to form a carboxylic acid and water

44
Q

preparing a ketone

A

secondary alcohol heated under reflux with an oxidising agent and acidified potassium dichromate to make a ketone and water

45
Q

nucleophile

A

species that donates a lone pair of electrons

46
Q

organohalogen compounds

A

molecules that contain at least one halogen atom joined to a carbon chain.

47
Q

molecular ion

A

positive ion formed when a molecule loses an electron

48
Q

molecular ion peak

A

clear peak at the highest m/z value on the right hand side of the mass spectrum

49
Q

fragmentation

A

when molecular ions break down into smaller pieces

50
Q

what are the year 1 reaction mechanisms?

A

radical substitution
electrophilic addition
nucleophilic substitution