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
sigma bond
the result of the overlap of two orbitals, one from each bonding atom
26
effect of greater chain length
more surface points of contact stronger London forces requires more energy to break bonds
27
effect of more branching
less surface points of contact weaker London forces requires less energy to break bonds
28
stages of radical substitution
initiation, propagation, termination
29
pi bond
sideways overlap of two p orbitals preventing them from rotating around the double bond
30
stereoisomers
same structural formula but different arrangement in space
31
E isomers
highest priority groups diagonally placed across the double bond
32
Z isomers
highest priority groups on the same side of the double bond
33
cis isomers
hydrogen atoms and methyl group on each carbon in the double bond on the same side
34
trans isomers
hydrogen atoms and methyl groups diagonally opposite each other
35
hydrogenation of alkenes
alkene mixed with hydrogen to make an alkane
36
halogenation of alkenes
alkenes mixed with a halogen to make a haloalkane
37
hydration of alkenes
alkene add water to make an alcohol
37
electrophile
electron pair acceptor
38
carbocation
an ion that contains a positively charged carbon
39
primary alcohol
an alcohol in which the -OH is attached to a carbon atom with either two or 3 hydrogen atoms
40
secondary alcohol
an alcohol in which the -OH is attached to a carbon atom that is attached to two carbon chains and a hydrogen atom
41
tertiary alcohol
an alcohol in which the -OH is attached to a carbon atom that is attached to three carbon atoms and no hydrogen atoms
42
preparing an aldehyde
distillation of a primary alcohol with an oxidising agent and acidified potassium dichromate to make an aldehyde and water
43
preparing a carboxylic acid
primary alcohol heated under reflux with an oxidising agent and acidified potassium dichromate to form a carboxylic acid and water
44
preparing a ketone
secondary alcohol heated under reflux with an oxidising agent and acidified potassium dichromate to make a ketone and water
45
nucleophile
species that donates a lone pair of electrons
46
organohalogen compounds
molecules that contain at least one halogen atom joined to a carbon chain.
47
molecular ion
positive ion formed when a molecule loses an electron
48
molecular ion peak
clear peak at the highest m/z value on the right hand side of the mass spectrum
49
fragmentation
when molecular ions break down into smaller pieces
50
what are the year 1 reaction mechanisms?
radical substitution electrophilic addition nucleophilic substitution