4.1.1 Basic concepts & 4.1.2 Alkanes Flashcards

(38 cards)

1
Q

Hydrocarbon

A

contains H and C only

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2
Q

staturated

A

contains only C-C single bonds

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3
Q

unsaturated

A

contains at least one c=c double or triple bond

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4
Q

Aliphatic

A

contains C atoms joined in straight or branched chains - not a benzene ring

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5
Q

Alcytic

A

aliphatic molecule that contains C atoms joined in a ring but not a benzene ring

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6
Q

Aromatic

A

contains at least one benzene ring

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7
Q

Alkanes general formulae

A

CnH2n+2

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8
Q

how to draw skeletal formualae

A

dont draw carbons or H

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9
Q

ethane structural formulae

A

CH3CH3

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10
Q

how is a sigma bond formed

A

by overlapping orbitals between bonding atoms

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11
Q

can sigma bonds rotate

A

yes they can freely rotate

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12
Q

how is a Pi bond formed

A

formed by overlapping P orbitals above and below bonded atom

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13
Q

can Pi bonds rotate

A

No

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14
Q

what bonds make a double bond

A

Pi and sigma

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15
Q

what bond makes a single bond

A

Sigma

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16
Q

Bond fission definition

A

breaking covalent bonds

17
Q

Homolytic fission definition

A

where covalent bond breaks and one of the bonding electrons moves to each atom forming 2 radicals

18
Q

radical

A

species with at least one unpaired electron

19
Q

a fish

A

hook arrow representing movement of 1 electron

20
Q

Heterolytic fission

A

covalent bond breaks and both bonding electrons go to one of the atoms forming an anion and a cation

21
Q

what does a curly arrow represent

A

movement of a pair of electrons when a covalent bond is broken or formed

22
Q

mechanism definition

A

shows which covalent bonds are being broken and made

23
Q

3 types of reactions

A

substitution
addition
elimination

24
Q

substitution reaction

A

1 element is replaced by another in a molecule

25
addition reaction
where theres fewer products than reactants
26
elimination reaction
where theres one more product than reactants
27
what state are the first 4 alkanes
gases
28
what happens to the boiling point as the alkane gets bigger and why
increases as number of carbons increases due to there being more IMF that need more energy to overcome
29
strongest IMF in an alkane
London forces
30
do larger molecules have stronger or weaker london forces and why
stronger as they have more electrons
31
why do branched alkanes have lower melting points than straight chained alkanes
straight chained have more points of contact so there's more london forces so more energy is required to overcome the IMF
32
what does complete combustion of an alkane form
carbon dioxide and water
33
what does incomplete combustion of alkane form
Carbon monoxide and water
34
Free Radical substitution steps
initiation propagation termination
35
chlorination of methane initiation step
Cl2 -> 2Cl*
36
chlorination of methane propagation step
Cl* + CH4 -> CH3* + HCl CH3* + Cl2 -> CH3Cl + Cl*
37
what is the termination
add the radicals together to make Cl2 CH3Cl C2H6
38
Limitations of free radical substitution
further substitutions can occur creating unwanted products from the radicals