Ch13 Hydrocarbons- alkane Flashcards

1
Q

5 Fuel properties

A
  1. have high energy output
  2. be either abundant or manufactured easily
  3. be easy to transport and store
  4. be easy to ignite
  5. cause minimum environmental damage
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2
Q

Saturated compound

A

a molecules in which all the atoms are linked together by single sigma bonds only

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3
Q

hydrocarbon

A

compound that contains hydrogen and carbon only

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4
Q

Trend in boiling point of alkane

A

Increases as Mr gets larger
- increased chain length and therefore increased electrons present
- more London dispersion forces so more energy required to overcome them

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5
Q

Trend in boiling point as branching increases

A

decreases as degree of branching increases
- less branched can pack together more tightly so have increased surface contact
- creates more London dispersion forces
- more energy is needed to overcome intermolecular forces

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6
Q

solubility of alkanes

A

insoluble in polar solvents
- low polarity so don’t mix with polar molecules

dissolve readily in each other as molecules link through induced dipole-dipole interactions

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7
Q

Alkanes chemical properties

A

unreactive
- CH bonds have low polarity
- single bonds linking CH are relatively strong

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8
Q

Combustion of alkanes in excess of oxygen

A

produces carbon dioxide and water

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9
Q

Combustion of alkanes in limited supply of oxygen

A

produces carbon monoxide/carbon and water

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10
Q

Carbon monoxide

A

poisonous - restricts effectiveness of blood to transport oxygen to body as binds with haemoglobin

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11
Q

Carbon

A

Soot- global dimming

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12
Q

Radical

A

particle that has at least one unpaired electron
highly reactive

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13
Q

substitution reaction

A

an atom(or group) is replaced by another atom

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14
Q

Conditions of radical substitution

A

ultraviolet radiation

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15
Q

Steps in radical substitution

A
  1. initiation - starts reaction by forming a radical
  2. propagation- maintains reaction by forming one of the products a new radical
  3. termination - ends reaction by removing the radicals and forming molecules
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16
Q

Homolytic fission

A

when covalent bond is broken so that the atoms joined by covalent bond each take one of the shared electrons

17
Q

Initiation

A

UV radiation provides sufficient energy to break covalent bond via homolytic fission, forming 2 radicals

18
Q

Propogation

A

in first reactions produces hydrogen halide and alkyl radical

in second always produces organic product and regenerates halogen radical