organic chemistry Flashcards

(41 cards)

1
Q

what is crude oil?

A

a finite resource found in rocks made from a mixture of very large number of compounds- particulary hydrocarbon compounds (mostly alkanes)

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2
Q

how is crude oil formed?

A

over millions of years from effects of high pressure and temperature on remains of biomass - mainly plankton that was buried in mud

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3
Q

what are hydrocarbons?

A

compounds that contain hydrogen and carbon atoms ONLY

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4
Q

name first 4 alkanes

A
  • methane
  • ethane
  • propane
  • butane

monkey eat peanut butter

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5
Q

formula for alkanes

A

CnH2n+2

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6
Q

how can hydrocabons be separated in crude oil?

A

by fractional distillations into fractions that can be used to produce fuels and feedstosckl fro petrochemical industry

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7
Q

describe process of frational distiallation

A
  1. crude oil heated and vapourised
  2. vapours of hydrocarbons enter fractationing coloum that has temperature gradient
  3. vapours of hydrocarbons with high boiling points condense at bottom
  4. vapours of hydrocarbons with lower boiling points rise amd condense at top

temperature gradient- hot at bottom, cold at top

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8
Q

what is made from petrochemical industry

A
  • polymers
  • lubricants
  • solvents
  • detergents
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9
Q

what is made from crude oil- what are the fractions and their usages
order from top to bottom

A
  • liquified petroleum gas- domestic heating and cooking
  • petrol- fuel for cars
  • kerosene- jet feul
  • diesel- diesel engines
  • heavy fuel oil- ships & power stations
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10
Q

what properties of hydrocarbons depend on molecule size and what are their trends

A
  • viscosity- ^ hydrocarbons ^ viscosity
  • due to increased intermolecular forces
  • better lubricants, but not useful as fuel
  • flammability- ^hydrocrabons , flammability
  • useful as fuels
  • boiling points- ^hydrocrabons ^boiling points
  • increased intermolecular foces- ^energy
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11
Q

complete combustion of hydrocarbons:

A
  • releases energy
  • H & C oxidised to form water & carbon dioxide
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12
Q

what is cracking

A

hydrcarbons broken down to produce smaller, more useful molecules as demand for short chain hydrocarbons are more

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13
Q

2 types of cracking
and their conditions

A

Catalytic cracking
- high temperatures
- catalyst
Steam cracking
- high temperature
- steam

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14
Q

what does cracking produce

A

alkanes AND alkene

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15
Q

why are alkenes more useful?

A
  • used to make polymers
  • starting material for other chemicals
  • more reactive than alkane
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16
Q

how to test for alkene

A

in bromine water
will turn colourless

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17
Q

formula for alkene

18
Q

alkane vs alkene

A
  • alkane
  • alkene
  • alkane- saturated
  • alkene- unsaturated- fewer H atoms
  • alkane- single carbon bonds
  • alkene- carbon double bond
19
Q

combustion of alkene
reaction w o2

A

can be compete or incomplete
incomplete more often’
^ smoky flame

20
Q

hydrogenation of alkene
required conditions and outcome

A
  • 150^C
  • nickel catalyst
  • alkene + hydrogen -> alkane (single bonds now)
21
Q

hydration of alkene
required conditions and outcome

A
  • 300^C
  • 70atm- pressure
  • water as steam
  • phosporic acid as catcalyst
  • alkene + steam (water) <> alcohol (reversible)
22
Q

halogenation of alkene

A
  • rapidly
    di(halogen)(alkane)
  • dichloroethane
  • double -> single
23
Q

alcohol functional group

24
Q

alcohol condesed formulaes

A

CH3OH
CH3CH2OH
CH3CH2CH2OH
CH3CH2CH2CH2OH

25
2 ways to amke ethanol pros and cons
hydration - + high yield of ethene - - high temp ^energy - - crude oil- non renewabe fermentation ~ glucose -yeast/30^C-> ethanol + CO2 - + low temp, less energy - + sugar from plant- renewable - - ethanol- aqueous solition- needs to be purified by distillation which required energy
26
alcohols and solubility
- soluble in water - ^ no, carbon atoms, DECREASE in solubility
27
alcohol + sodium
sodium (eth)oxide + hydrogen
28
alcohol -(oxidising agent)->
carboxylic acid + water
29
alcohol and combustion
- CO2 & H2O
30
functional group of carboxylic acid
COOH C=O !.... OH
31
carboxylic acid condensed formulas
HCOOH CH3COOH CH3CH2COOH CH3CH2CH2COOH
32
carboxuylic acids in water
- partially ionise -^ weak acids
33
alkane- ethane alkene alcohol carboxylic acid ester
- alkene- ethene - alcohol- ethanol - carboxylic acid- ethanoic acid - ester- ethyl ethanoate
34
alcohol + metal carbonate (ethanoic aci + sodiu carbonate)
-> (sodium ethanoate) + CO2 + water
35
carboxylic acid + alcohol
-> ester + water | SULFURIC ACID AS CATALYST!!!1
36
addition polymers
- monomers- alkenes - double -> single
37
condensation polymers
- monomers with 2 functional groups and wqhen reacting- the loose small molecules such as water - simplest- 2 monomers, each with 2 of same functiona groups - functionsl groups react with blank boxes for rest of formula - eg, OH + COOH -> ester + water ^ polyester joined together
38
amino acids- polymerisation
condenation polymerisation-> polypeptides due to 2 diff functional groups
39
diff amino acids joined in one chain
- protein
40
what is dna made up from
2 polymer chains made by monwers called nucleotide, wrapped around in a double helix - 2 diff types of monomers- ACTG
41
3 natural occuring polymers
proteins- monomers of amino acids starch- monomers of glucose cellulose- monomers of glucose