4.1.1 Basic concepts & 4.1.2 Alkanes Flashcards

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
Q

addition reaction

A

where theres fewer products than reactants

26
Q

elimination reaction

A

where theres one more product than reactants

27
Q

what state are the first 4 alkanes

A

gases

28
Q

what happens to the boiling point as the alkane gets bigger and why

A

increases as number of carbons increases due to there being more IMF that need more energy to overcome

29
Q

strongest IMF in an alkane

A

London forces

30
Q

do larger molecules have stronger or weaker london forces and why

A

stronger as they have more electrons

31
Q

why do branched alkanes have lower melting points than straight chained alkanes

A

straight chained have more points of contact so there’s more london forces so more energy is required to overcome the IMF

32
Q

what does complete combustion of an alkane form

A

carbon dioxide and water

33
Q

what does incomplete combustion of alkane form

A

Carbon monoxide and water

34
Q

Free Radical substitution steps

A

initiation
propagation
termination

35
Q

chlorination of methane initiation step

A

Cl2 -> 2Cl*

36
Q

chlorination of methane propagation step

A

Cl* + CH4 -> CH3* + HCl
CH3* + Cl2 -> CH3Cl + Cl*

37
Q

what is the termination

A

add the radicals together to make Cl2
CH3Cl
C2H6

38
Q

Limitations of free radical substitution

A

further substitutions can occur creating unwanted products from the radicals