UNIT 3: SECTION 2 - ALKANES & HALOGENOALKANES Flashcards

1
Q

What is an alkane?

A

Hydrocarbon with formula CnH2n

Forms maximum bonds with hydrogen

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2
Q

What are the order of fractions?

A

GAY - Gas
POLICEMEN - Petrol
NEVER - Naptha
KILL - Kerosene
GAY - Gas Oil
MEN - Mineral Oil
BITCH - Bitumen

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3
Q

Conditions for thermal cracking?

A
High temp (1000°C)
High pressure (70atms)
Mostly alkenes - polymerisation -> polymers such as plastic: poly(ethene).
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4
Q

Conditions for catalytic cracking AND one advantage?

A

High temp (450°C)
Slight pressure
Mostly aromatic HC’s and motor fuels
Uses zeolite catalyst

Cost-Efficient!

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5
Q

One use of alkanes,
and how they are used in this way?

One risk to this use?

A

Alkanes are good fuels.
Products are CO2 (POLLUTANT) and H2O and a lot of energy.

  • Used in power-stations, car engines etc.
  • If not enough O2, incomplete combustion occurs, leading to more pollutants.
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6
Q

4 Pollutants other than CO2 which are produced during the incomplete combustion of alkanes?

A

1) CO - Poisonous gas, binds to haemoglobin -> lowers O2 saturation.
[REMOVED VIA CAT. CONVERTERS]

2) Carbon - Soot, causes respiratory issues and engine buildup.

3) Smog - Unburnt HC + NOx
[NOx made in engine; high pressure high temp]
[REMOVED VIA CAT. CONVERTERS]

4) Acid Rain - SO2 from burning of fossil fuels.
SO2 dissolves in air -> H2SO4 -> RAINS.

  • Acid rain destroys vegetation, buildings, aquatic life.
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7
Q

What are free radicals?

A

Atoms with unpaired electrons, eg. *Cl

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8
Q

How are free radicals formed?

A

UV light + Halogen molecule -> 2Rads.

Photochemical reaction

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9
Q

How are halogenoalkanes formed and what type of reaction is this?

A

Halogen + Alkane ———> Halogenoalkane + Hydrogen

Free-rad substitution

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10
Q

The 3 stages of free radical reactions?

A

1) Initiation:
Cl2 (+UV) ———> 2Cl*

2) Propagation: Chain reaction…
Cl* + CH4 —> CH3* + HCl
CH3* + Cl2 —> CH3Cl + Cl*
And so on.. until all molecules of Cl/CH4 used up.

3) Termination: Free rads used up..
Cl* + CH3* —> CH3Cl
OR
CH3* + CH3* —> C2H6

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11
Q

What is a CFC? Why are they bad?

What is the reaction between CFC’s and O3?

A

CFC’s are chlorofluorocarbons -
All H’s replaced.

They were used in refrigerator coolants, aerosol sprays etc.

Damaged the Ozone layer.

1) CFCl3 (+UV) —> CFCl2* + Cl*
2) Cl* + O3 —> ClO* + O2
3) ClO* + O3 —> 2O2 + Cl*

Overall: 2O3 —> 3O2 (Cl* Catalyst)

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12
Q

What is O3?

How is it useful?

A

Ozone; found in Ozone layer -
ACTS AS CHEMICAL SUNSCREEN;
PREVENTS SKIN CANCER BY ABSORBING LOTS OF HEAT.

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13
Q

What are CFC alternatives?

A

HFC’s

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14
Q

Is the bond between a halogen and carbon polar?

If so, what causes this polarity?

A

It is polar because there is a high difference in ELECTRONEGATIVITY.

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15
Q

What is a nucleophile?

A

Electron donor.

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16
Q

What occurs in a nucleophilic substitution reaction?

A

Nucleophile replaces Halogen.

17
Q

Conditions to make Alcohol from Halogenoalkane?

A
  • Weak OH base.
  • Warm Aqueous soln.
  • Warm under reflux.
18
Q

Conditions to make Nitrile from Halogenoalkane?

A
  • CN
  • Ethanoic soln.
  • Warm under reflux.
19
Q

How do you make an Amine from a Halogenoalkane?

2 Step Mechanism; what is the process?

A
  • Ethanoic Soln.
  • Excess Ammonia (NH3)
  • Warm under reflux.

NH3 attracted to polarity in halogenoalkane bond. Replaces halogen.

N has +charge (4 atoms bonded to it)
Excess NH3 takes a H from NH3 bonded to HAlkane.
H donates electrons to HAlkane and leaves.

20
Q

What is an elimination reaction?
How does it work?
What are the conditions?

A

Elimination reactions take a hydrogen away from the HAlkane; hydrogen leaves its electrons - electrons fed to carbon chain - halogen leaves with its electrons.

Results in alkenes being formed.

Conditions:

  • OH
  • in ethanoic soln.
  • warmed under reflux
21
Q

If a mixture of water and ethanol is used in the reaction mixture, what products are made?

A

Mixture of alkenes and alcohols made.