6 - organic Flashcards

1
Q

hydrocarbon

A

a compound that contains only carbon and hydrogen atoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

saturated

A

refers to a compound containing only single bonds e.g. alkane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

unsaturated

A

refers to a compound containing one or more multiple bonds e.g. alkene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

multiple bond

A

two or more covalent bonds between two atoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

displayed formula

A

shows every atom and every bond

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

structural formula

A

shows (unambiguously) how the atoms are joined together

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

skeletal formula

A

shows all the bonds between carbon atoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

molecular formula

A

shows the actual number of each atom in the molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

empirical formula

A

shows the numbers of each atom in the simplest whole-number ratio

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

functional group

A

an atom or group of atoms in a molecule that is responsible for its chemical reactions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

homologous series

A

a family of compounds with the same functional group, which differ in formula by CH2 from the next number

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

prefix

A

a set of letters written at the beginning of a name

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

suffix

A

a set of letters written at the end of a name

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

locant

A

a number used to indicate which carbon atom in the chain an atom or group is attached to

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

structural isomers

A

compounds with the same molecular formula but with different structural formulae

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

stereoisomers

A

compounds with the same structural formula (and the same molecular formula), but with the atoms or groups arranged differently in three dimensions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

geometric isomers

A

compounds containing C=C bond with atoms or groups attached at different positions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

restricted rotation

A

restricted rotation around a C=C bond fixes the position of the atom or groups attached to the C=C atoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

fractional distillation

A

the process used to separate a liquid mixture into fractions by boiling and condensing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

cracking

A

the breakdown of molecules into shorter ones by heating with a catalyst

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

reforming

A

the conversion of straight-chain hydrocarbons into branched-chain and cyclic hydrocarbons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

complete combustion

A

means that all of the atoms in the fuel are fully oxidised

23
Q

incomplete combustion

A

means that some of the atoms in the fuel are not fully oxidised

24
Q

biofuels

A

fuels obtained from living matter that has died recently

25
non-renewable
energy sources that are not being replenished, except over geological timescales
26
biodiesel
a fuel made from vegetable oils obtained from plants
27
bioalcohols
fuels made from plant matter, often using enzymes or bacteria
28
renewable
uses sources that can be continuously replaced
29
substitution reaction
one in which an atom or group is replaced by another atom or group
30
mechanism
the sequence of steps in an overall reaction. each step shows what happens to the electrons involved in bond breaking or bond formation
31
homolytic fission
the breaking of a covalent bond where each of the bonding electrons leaves with one species, forming a radical
32
radical
a species that contains an unpaired electron
33
initiation step
involves the formation of radicals, usually as a result of bond breaking caused by ultraviolet radiation
34
propagation steps
the two steps that, when repeated many times, convert the starting materials into the products of a reaction
35
termination step
involves the formation of a molecule from two radicals
36
sigma bonds
covalent bonds formed when electron orbitals overlap axially (end-on)
37
pi bonds
covalent bonds formed when electron orbitals overlap sideways
38
addition reaction
a reaction in which two molecules combine to form one molecule
39
hydrogenation
involves the addition of hydrogen
40
halogenation
involves the addition of a halogen
41
hydration
involves the addition of water (or steam)
42
diol
a compound containing two OH (alcohol) groups
43
curly arrows
represent the movement of electron pairs
44
electrophile
a species that is attracted to a region of high electron density
45
electrophilic addition
a reaction in which two molecules form one molecule and the attacking molecule is an electrophile
46
heterolytic fission
the breaking of a covalent bond so that both bond electrons are taken by one atom
47
carbocation
a positive ion in which the charge is shown on a carbon atom
48
electron-releasing group
pushes electrons towards the atom it is joined to
49
monomers
small molecules that combine together to form a polymer
50
repeat unit
the set of atoms that are joined together in large numbers to produce the polymer structure
51
recycling
involves converting polymer waste into other materials
52
incinerator
converts polymer waste into energy
53
biodegradable polymer
one that can be broken down by microbe
53
use as a feedstock (?)
involves converting polymer waste into chemicals that can be used to make new polymers