Unit 3 Module 4.1 Flashcards

(48 cards)

1
Q

rules for organic chemistry

A

find the longest continuous chain
name the chain coming off
count which carbon this from- lowest
does the same chain come off more than once
chains named alphabetically
any functional groups go at the end of the name

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2
Q

what does aliphatic mean

A

carbon chains

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3
Q

what does alicyclic mean

A

carbon atoms in a ring structure

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4
Q

what does aromatic mean

A

involves benzene rings

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5
Q

what does homologous series mean

A

a series of organic compounds having the same functional group but with each successive member differing by CH2

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6
Q

what is molecular formula

A

counts the numbers of each sort of atoms present

C4H10

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7
Q

what is displayed formula

A

shows all the bonds in the molecule

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8
Q

what is structural formula

A

allows you to work out the structure

CH3CH2CH3

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9
Q

what is a structural isomer

A

molecules with the same molecular formula but different structural formula

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10
Q

what is position isomerism

A

basic carbon skeleton is unchanged but important groups are moved around the skeleton

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11
Q

how do bonds form in alkanes

A

the overlap of orbitals gives sigma bonds- these bonds can freely rotate

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12
Q

algebraic formula for balancing complete combustion equations

A

CxHy + (x+y/4)O2 +y/2 H2O

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13
Q

what is a radical

A

a species with an unpaired electron

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14
Q

what is the initiation reaction

A

chain initiated, by UV light breaking a chlorine molecule into free radicals (homolytic fission)

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15
Q

what is the substitution reaction

A

hydrogen atoms are replaced b cl or br atoms

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16
Q

what are propagation reactions

A

keep the chain going

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17
Q

what are termination reactions

A

remove free radicals from the system

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18
Q

what do double bonds do to a molecule

A

puts a kink in the chain, so the molecules cant pack together so tightly- weaker intermolecular forces

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19
Q

how does a double bond form

A

sigma and pi bond- pi bond formed from the overlap of p orbitals and stops rotation

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20
Q

define isomerism

A

molecules with the same molecular formula, but different structural formula

21
Q

define position isomerism

A

basic carbon skeleton remains unchanged but important groups move around the skeleton

22
Q

define stereoisomerism

A

same structural formula but a different arrangement in space

23
Q

two types of stereoisomerism

A

cis and trans

E and Z

24
Q

what must be there for E Z isomerism

A

C=C

different groups attached to each C in the double bond

25
what is the difference between E and Z isomerism
Z- they're on the same side | E- they're on opposite sides
26
what must there be for cis and trans isomerism
C=C each C must be attached to 2 different groups but one of these groups on each C must be a H
27
what is the difference between cis and trans
cis- on the same side | trans- on different sides
28
what is the Cahn-ingold-Prelog priority rule
higher atomic number gives atom priority
29
what happens with addition reactions with hydrogen
hydrogenation
30
what reactions do alkanes undergo
combustion | substitution
31
what reactions do alkenes undergo
combustion | addition
32
why are alkenes attacked by electrophiles
high electron density of double bond means alkenes are attacked by electrophiles
33
what is an electrophile
electron pair acceptors
34
what is a carbocation
positive carbon formed in addition mechanism
35
bond fission in electrophilic addition
heterolytic
36
what is markovnikoffs rule
hydrogen atoms will attach itself to the carbon atom of the alkene with greater number of H atoms and fewer number of C atoms
37
which is more energetically stable secondary or primary carbocation
secondary- less activation energy is needed
38
what is polymerisation
when an alkene undergoes addition reactions with itself to form a polymer conditions- high temp, high pressure
39
what decides the properties of a polymer
chain length side groups branching
40
uses of polymers
windows, electrical insulation, cups, plastic bags
41
ways of processing waste polymers
combustion for energy production organic feedstock removal of toxic waste products biodegradable and photodegradable polymers
42
what is heterolytic fission
breaking of a covalent bond, where one atom gets both of the shared electrons
43
what is homolytic fission
when a covalent bond breaks, each atoms gets one of the shared electrons- creating free radicals
44
what does a curly double headed arrow represent
the movement of a pair of electrons
45
+ve and -ve of combustion for energy production
removes polymers, heat energy produces, saves fossil fuels | CO2 produced, toxic gases
46
+ve of organic feedstock
breaks down polymers without separating them, reduces amount of crude oil used
47
+ve and -ve of removal of toxic waste products
removes polymer, neutralises toxic products, generates power, saves fossil fuels expensive
48
+ve and -ve of biodegradable and photodegradable polymers
biodegradable, less fossil fuels used | long time, small fragments eaten by animals