organic chemistry Flashcards

(63 cards)

1
Q

What is a hydrocarbon?

A

A hydrocarbon is a molecule made up of only hydrogen + carbon

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2
Q

why type of bonds do alkanes have?

A

single covalent bonds

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3
Q

what is the alkane formula

A

CnH2n+2

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4
Q

how many bonds can carbon form?

A

4 bonds

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5
Q

what is CH4 called ?

A

methane

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6
Q

what is a homologous series?

A

a group of hydrocarbons with a similar function group and therefore similar properties e.g alkAnes, alkEnes, alcOHOLS

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7
Q

what are the first 6 alkanes

A
1= methane 
2= ethane
3=propane
4=butane
5=pentane
6=hexane
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8
Q

what is a structural isomer?

A

molecules that have the same molecular formula but a different structural formula i.e the order the atoms are connected to the chain is differnt.

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9
Q

the longer the hydrocarbon the_____ the surface area

A

bigger

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10
Q

the larger the surface area the______ the number of intermolecular forces.

A

higher

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11
Q

the greater the number of intermolecular forces the _____ the energy required to break them.

A

higher

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12
Q

the more energy required to break the intermolecular forces the ____ boiling point

A

higher

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13
Q

what type of bond is present in an alkene

A

a double bond

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14
Q

what is the general formula for an alkene ?

A

CnH2n

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15
Q

if the double bond was on the first carbon of an alkene with 4 carbons what would you name it?

A

but-1-ene

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16
Q

are alkanes saturated and why?

A

alkanes are saturated because every spare bond is attached to a hydrogen

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17
Q

are alkenes saturated and why?

A

alkenes unsaturated because they contain a double bond and therefore have less carbon atoms

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18
Q

what is a symmetric alkene?

A

semetric alkenes have the same groups on each side of a double bond

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19
Q

what is an asymmetric alkene

A

asymmetric alkenes have different groups on each side of the double bond.

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20
Q

what is a geometric isomer in an alkene ?

A

geometric isomers is where there are the same groups on each side of them double bond however they have a different arrangement.

  • this is because the double bond does not rotate
  • same structural formula
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21
Q

what is a cis geometric isomer ?

A

cis is where the alkene has matching groups on the same side of the bond (if you draw out the skeletal formula it makes a c shape)

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22
Q

what is a trans geometric formula?

A

trans is where the matching groups are on opposite sides of the bond

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23
Q

z

A
  • together

‘zame zide’

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24
Q

E

A

separate

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25
tetrahedral , area of electron density and angle
4 and 109.5 degrees
26
trigonal planar ,area of electron density and angle
3 and 120
27
linear ,area of electron density and angle
2 and 180
28
where are sigma bond found and what are they
they are found in alkanes (single bonds)
29
which is the strongest, sigma or pi bonds?
sigma bond because there is a greater overlap
30
which is shortest a double bond or a single bond
a single bond
31
electrophile
a molecule or atom which is attracted to a negative charge and can accept a lone pair of electrons to form a covalent bond
32
electrophilic addition
atoms or ions are added across the bond. no atoms are lost. this can happen because the carbon is double bonded double bond opens up to allow a molecule to join on.
33
carbocation
ion with a positively charged carbon atom
34
polarised
when a molecule becomes positive at one end and negative at the other
35
curly arrow
shows the movement of an electron pair
36
what is a stable carbocation
a carbon cation which is attached to the most carbon atoms (has the most electrons donated)
37
what do alkyl groups do? (carbon groups)
they have an electron donating effect
38
electron configuration
1s, 2s, 2p, 3s, 3p, 4s, 3d
39
p orbitals
2px 2py 2pz
40
max electrons in s
2
41
max electrons p holds
6
42
max electrons d holds
10
43
Each hybrid orbital contains 2 electrons ready for bonding true or false
true
44
Each hybrid orbital contains 2 electrons ready for bonding true or false
false only 1
45
P orbitals that are not hybridised can overlap to form pi bonds true or false
true
46
The number of hybrid orbitals formed is always 1 more than the number of orbitals used true or false
false, the same number
47
The superscript in sp3 tells you the number of s orbitals used to make the hybrid orbital. true or false
false the p orbitals
48
Carbons with 3 areas of electron density form linear shapes. true or false
false trigonal planar
49
how many orbitals in a tetrahedral molecule | hybridisation
one of the s orbitals and three of the p orbitals combine to form four hybrid sp orbitals making 4 sigma bonds
50
how many orbitals in a trigonal planar molecule | hybridisation
one of the s orbitals and two of the p orbitals combine to form three hybrid sp2 orbitals creating 3 sigma bonds.
51
how many orbitals in a linear molecule | hybridisation
one of the s orbitals and one of the p orbitals combine to form 2 hybrid sp orbitals creating 2 sigma bonds
52
What are the prefixes for branched alkanes with a chain length of 1 - 4 carbons? Eg methyl, ...
ethyl propyl butyl
53
What is a cycloalkane?
alkanes that have carbon atoms attached in a ring.
54
how do you test for an alkene ?
bromine water
55
What is electron pair repulsion theory?
The principle that electron pairs around a central atom tend to orient themselves as far apart as possible.
56
what are the three steps of a free radical ?
initiation, propagation, termination
57
conditions for free radical substitution
needs uv light to start the reaction (initiation stage)
58
What is heterolytic (bond) fission?
the breaking of a covalent bond in such a way that one atom gets both of the shared electrons - creates a + and a - ion
59
What is homolytic (bond) fission?
Homolytic fission is where each atom of the bond keeps an electron each resulting in species called free radicals
60
What is a polymer?
a long chain molecule that is formed from small molecules linking together
61
What is the name for the mechanism for making polymers?
polymerization
62
What is cracking?
Cracking is a reaction in which larger saturated hydrocarbon molecules are broken down into smaller, more useful hydrocarbon molecules
63
What are the two types of cracking?
Catalytic cracking uses a temperature of approximately 550°C and a catalyst known as a zeolite which contains aluminium oxide and silicon oxide. Steam cracking uses a higher temperature of over 800°C and no catalyst.