Chapter 12 - Alkanes (MODULE 4) Flashcards

(31 cards)

1
Q

What are alkanes

A

saturated hydrocarbons

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2
Q

what property of alkanes allows crude oil deposits to remain in the Earth for millions of years

A

they are usually very stable

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3
Q

What is the general formula of aliphatic alkanes

A

C(n) H (2n+2)

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4
Q

What are the names of the first ten alkanes

A

methane,
ethane
propane
butane
pentane
hexane
heptane
octane
nonane
decane

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5
Q

What type of covalent bond is present in alkanes
- How many of these does each carbon atom have in an alkane

A

sigma bonds
- 4

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6
Q

What is a sigma bond
- how many electrons are present

A

an overlap of 2 orbitals
- 2, one from each bonded atom

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7
Q

Where is the electron density in a sigma bond

A

between the two atoms

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8
Q

WHat is the shape and bond angle in an alkane

A

tetrahedral, 109.5 degrees

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9
Q

How do oil refineries separate crude oil

A

fractional distilation

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10
Q

How do boiling points of unbranched alkanes change as chain length increases

A

boiling point increases

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11
Q

What are London forces
- what is the relation between amount of London forces and boiling point for alkanes

A

weak intermolecular forces due to surface contact between molecules
- more London forces correlates to a higher boiling point

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12
Q

why does increasing chain length affect boiling point (3)

A

greater chain length -> greater surface contact
-> more London forces
-> higher boiling point

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13
Q

Why does increased branching decrease boiling point (4)

A

-> more branching -> less surface contact
-> less London forces
-> branching keeps molecules further apart from each other
-> lower boiling point

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14
Q

What are the 3 reasons for the lack of reactivity of alkanes

A

C-C and C-H sigma bonds are strong
- C-C bonds are non-polar
- electronegativity of carbon and hydrogen is so similar that C-H bond is considered non-polar

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15
Q

what is the general equation for the combustion of alkanes

A

alkane + oxygen -> carbon dioxide + water

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16
Q

Why are alkanes used as fuels

A

-> readily available
-> easy to transport
-> burn in a plentiful supply of oxygen without releasing toxic products

17
Q

WHat is the symbol equation for the complete combustion of methane and ethane

A

methane: CH4 + 2 O2 → CO2 + 2 H2O + energy
ethane: C2H6 + 3.5 O2→ 2CO2 + 3H2O

18
Q

What happens if combustion occurs when supply of oxygen is not plentiful
- what is formed

A

incomplete combustion
- carbon monoxide, carbon

19
Q

Why is CO harmful

A

it binds irreversibly with haemoglobin preventing it from transporting oxygen around the body

20
Q

Why is CO hard to detect

A

colourless and odorless

21
Q

What condition is required for alkanes to react with halogens
- What type of reaction is it

A

UV
- substitution

22
Q

What is the equation of the reaction between bromine and methane

A

CH4 + Br2 -> CH3Br + HBr

23
Q

What type of mechanism is the bromination of an alkane

A

radical substitution

24
Q

What are the three stages of radical substitution

A

initiation, propagation, termination

25
What happens in the initiation stage of bromination of methane
the Br2 molecule is broken by homolytic fission forming 2 bromine radicals
26
How are radicals represented
with a single dot
27
What happens in the propagation stage of bromination of methane
methane reacts with Br radical forming HBr and methyl radical. methyl radical reacts with Br2 making another Br radical and CH3Br cycle repeats
28
What happens in the termination stage of bromination of methane
one of three things happens stopping the reaction - Br radical + Br radical -> Br2 - CH3 radical + CH3 radical -> C2H6 CH3 radical + Br radical -> CH3Br
29
What is the main issue with using radical substitution to produce organic products
- Further substitution might occur e.g. Br radical may react with CH3Br eventually causing CH2Br2, CHBr3 and/or CBr4 to form
30
What is the problem with radical substitution with alkanes with 3 or more carbons
a mixture of isomers will form as the radical can attach to different carbons causing different products to form
31