10.2 Functional group chemistry Flashcards

1
Q

Combustion of alkanes and why they are used as fuels

A

Complete: CnH2n+2 + O2 -> CO2 + H2O

Incomplete: CnH2n+2 + O2 -> CO + H2O

Extreme limitation of O2: CnH2n+2 + O2 -> C + H2O

Because:

highly exothermic because much E released in fomring double bonds in CO2 and in H2O

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Explain greenhouse gases

A

CO2 and H2O (produced by combustion) are greenhouse gases - absorb infrared - contribute to global warming and climate change

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Explain global dimming

A

Unburned carbon released into air as small particles - form smog, affect respiratory system - contribute to global dimming

Global dimming: air pollution blocks sun’s rays - causes cooling effect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Explain substitution

A

SUBSTITUTION: usually with saturated

Ex: halogenation in 3 steps

  1. INITIATION: homolytic fission of halogen under UV
  2. PROPAGATION: halogen radical attacks alkane - Hhal + alkane radical -> alkane radical reacts with another halogen radical - halogenalkane
  3. TERMINATION: Two radicals combine: 2 halog radicals, 2 alkane radicals or halogen radical and alkane radical
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Explain addition reactions

A

Addition usually with unsaturated - alkenes - form different saturated products

Types of addition:

  • hydrogenation (H)
  • addition of halogens
  • addition of halogen halides (HBr, HCl…)
  • hydration (OH)
  • addition polymerisation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What could be synthesised from an alkene

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Combustion of alcohol

A

CnH2n+1OH + O2 -> CO2 + H2O

Combustion = complete oxidation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Oxidation of alcohols

A

Oxidising agent used (K2Cr2O7) to increase bonds with O -> double bond - alcohol to aldehyde/carboxylic acid/ketone

Primary OH -> alhehyde -> carboxylic

Secondary OH -> ketone

Tertiary alcohols are not oxidised

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Explain reflux

A

Reflux - involves condensation of vapours into fractions according to boiling temp

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Explain esterification

A

Esterification - production of ester via condensation

alchol + carboxylic acid -conc. H2SO4-> ester

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Explain nucleophilic substitution

A

In halogenalkanes due to polarity - partial charges in molecules

Nucleophiles are attracted to e defficient C in halogenalkane - substitution of halogen occurs

Types of reactions:

  • Sn1
  • Sn2
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Explaine electrophilic substitution

A

usually with benzene - dense delocalised e ring - electrophiles are defficient in e - attaracted to the ring - replace H in benzene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly