Module 4: Section 1 Flashcards

(44 cards)

1
Q

What is an isomer?

A

isomers have the same molecular formula but the atoms are arranged differently.

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2
Q

Name 2 types of isomer.

A

structural isomers and stereoisomers.

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3
Q

What are structural isomers?

A

structural isomers have the same molecular formula but a different structural formula (atoms connected in different ways).

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4
Q

Name 3 types of structural isomer.

A
  • chain isomer
  • positional isomer
  • functional group isomer
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5
Q

What are chain isomers?

A

the carbon skeleton is arranged differently e.g. as a straight chain or branched in different ways.
have similar chemical properties but different physical properties because of change in shape of molecule.

e.g. C4H10 can be butane or methyl propane

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6
Q

What are positional isomers?

A

functional group attached to a different carbon atom.
have different physical properties and chemical properties might be different too.

e.g. C4H10O can be butan-1-ol or butan-2-ol

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7
Q

What are functional group isomers?

A

same atoms arranged into different functional groups.
have very different physical and chemical properties.

e.g. C4H8O2 can be butanoic acid or methyl propanoate

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8
Q

What is the general formula of the alkanes?

A

CnH2n+2

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9
Q

Why are alkanes classed as hydrocarbons?

A

the contain hydrogen and carbon only

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10
Q

Why are alkanes saturated?

A

all the carbon-carbon bonds are single bonds

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11
Q

What is the general formula of cycloalkanes?

A

CnH2n

cycloalkanes have two fewer hydrogens than alkanes

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12
Q

What is the shape and bond angle around each carbon in alkanes?

A

in each alkane molecule, each carbon atom has four pairs of bonding electrons around it. They all repel each other equally so the molecule forms a tetrahedral shape around each carbon. Bond angle = 109.5°

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13
Q

What does the boiling point of an alkane depend on?

A

its size and shape

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14
Q

What physical state are small alkanes, like methane, at room temp and pressure?

A

gas - they’ve got very low boiling points

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15
Q

What physical state are larger alkanes at room temp and pressure?

A

liquid - they have higher boiling points

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16
Q

Why do larger alkanes have higher boiling points than smaller alkanes?

A

alkanes have covalent bonds between atoms inside the molecules. Between molecules, there are London forces (induced dipole-dipole forces) which hold them all together. The longer the carbon chain, the stronger the London forces because there’s more surface contact and more electrons to interact. It take more energy to overcome these London forces and the boiling point rises.

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17
Q

Why does a branched-chain alkane have a lower boiling point than its straight chain isomer?

A

branched-chain alkanes can’t pack closely together and they have smaller molecular surface areas so London forces are reduced.

(unbranched alkane molecules can pack closely together so there is a lot of surface contact)

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18
Q

What is produced when alkanes are burnt (oxidised) completely in oxygen?

A

carbon dioxide + water

19
Q

What type of reaction is it?

A

combustion reaction

20
Q

Why do liquid alkanes need to be vaporised before combustion?

A

combustion reactions happen between gases, so liquid alkanes have to be vaporised first

21
Q

How are smaller alkanes described as they turn into gases more easily?

A

smaller alkanes are more volatile (so they’ll burn more easily too)

22
Q

Why do larger alkanes release more energy per mole when they’re combusted?

A

they have more bonds to react

23
Q

Why do alkanes make good fuels?

A

they release so much energy when they burn

24
Q

What is produced when alkanes are burnt in limited oxygen?

A

carbon monoxide + water

25
Why is carbon monoxide a problem?
carbon monoxide is poisonous. Haemoglobin transports oxygen around the body in the blood. Carbon monoxide is better at binding to haemoglobin than oxygen is, so it binds to haemoglobin in the blood before oxygen can so less oxygen can be transported around the body, leading to oxygen deprivation. High concentrations of CO can be fatal.
26
What is bond fission?
breaking a covalent bond
27
What are the two types of bond fission?
heterolytic fission and homolytic fission
28
What is heterolytic fission?
the bond breaks unevenly with one of the bonded atoms receiving both electrons from the bonded pair. A positively charged cation and a negatively charges anion are produced.
29
What is homolytic fission?
the bond breaks evenly and each bonded atom receives one electron from the bonded pair. Two electrically uncharged 'radicals' are formed.
30
What is a radical?
a particle with an unpaired electron. Because of the unpaired electron, radicals are very reactive. (shown in mechanisms by a big dot next to the molecular formula, dot represents the unpaired electron)
31
What is produced when halogens react with alkanes?
halogens react with alkanes, in photochemical reactions, to produce haloalkanes. A hydrogen atom is substituted by chlorine or bromine
32
What is a photochemical reaction?
reaction started by light
33
What does a reaction between a halogen and an alkane require to start?
ultraviolet light
34
What type of reaction is it between a halogen and alkane?
free-radical substitution reaction
35
What is the general formula for alkenes?
CnH2n
36
Why are alkenes classed as hydrocarbons?
they contain carbon and hydrogen only
37
Why are alkenes unsaturated?
they contain at least one carbon=carbon double bond
38
Why are molecule 'unsaturated'?
molecules with C=C double bonds are unsaturated because they can make more bonds with extra atoms in addition reactions
39
How does a cyclic alkene differ from an open-chain alkene?
a cyclic alkene has 2 fewer H atoms
40
How is a sigma bond formed?
a sigma bond is formed when two s orbitals overlap. The two s orbitals overlap in a straight line - this gives the highest possible electron density between the two nuclei. This is a single covalent bond. High electron density between the nuclei means there is a strong electrostatic attraction between the nuclei and the shared pair of electrons. So sigma bonds have a high bond enthalpy - strongest type of covalent bond. (C-C and C-H bonds in alkanes are all sigma bonds)
41
How is a pi bond formed?
a pi bond is formed by the sideways overlap of two adjacent p orbitals. It's got 2 parts - one 'above' and one 'below' the molecular axis because the p orbitals that overlap are dumb-bell shaped. Pi bonds are much weaker than sigma bonds because the electron density is spread out above and below the nuclei. So the electrostatic attraction between the nuclei and the shared pair of electrons is weaker, so pi bonds have a relatively low bond enthalpy.
42
Why are alkanes so unreactive?
- alkanes only contain C-C and C-H sigma bonds, which have a high bond enthalpy and so are difficult to break. - the bonds are also non-polar so they don't attract nucleophiles or electrophiles, so alkanes don't react easily
43
Why are alkenes more reactive than alkanes?
- alkenes are more reactive because the C=C bond contains both a sigma and a pi bond - the C=C bond contains 4 electrons so has a high electron density and the pi bond also sticks out above and below the rest of the molecule, these two factors mean the pi bond is likely to be attacked by electrophiles - the low bond enthalpy of the pi bond also contributes to reactivity of alkenes
44
Why are alkenes useful?
because the double bond is so reactive, alkenes are good starting points for making other organic compounds and for making petrochemicals