7: Organic Chemistry Flashcards

1
Q

what is a hydrocarbon?

A

compounds that only contain hydrogen and carbon atoms

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2
Q

what is a homologous series?

A

a series of organic compounds w similar features & chemical properties due to them having the same functional group

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3
Q

describe how crude oil is formed.

A

is formed over millions of years from the effects of high pressures and temperatures on the remains of plants and animals

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4
Q

what is an alkane and what is its formula?

A

a homologous series of hydrocarbon compounds with only single carbon bonds - making them saturated hydrocarbons; formula = CnH2n+2

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5
Q

what reactions can alkanes undergo?

A

combustion; can be cracked into smaller molecules; react with halogens in the presence of light

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6
Q

what are the first four alkanes and their structural formulas?

A

methane - CH4; ethane - CH3CH3; propane - CH3CH2CH3; butane - CH3CH2CH2CH3

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7
Q

what is the equation for combustion w methane?

A

CH4 + 2O2 → CO2 + 2H2O

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8
Q

describe how fractional distillation works to separate crude oil.

A
  1. a fractionating column is v hot at bottom & cool at top
  2. crude oil enters fractionating column & is heated -vapours rise
  3. vapours of hydrocarbons w v high boiling points will immediately condense into liquid at higher temp lower down & are tapped off at the bottom of the column.
  4. vapours of hydrocarbons w low boiling points will rise up column & condense at the top to be tapped off.
  5. different fractions condense at different heights according to boiling points & are tapped off as liquids.
  6. fractions containing smaller hydrocarbons are collected at top of fractionating column as gases; and vice versa
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9
Q

why do we need to separate crude oil?

A

as a mixture it isn’t very useful; but as fractions, they all have different uses

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10
Q

what can the fractions of crude oil be used for?

A

polymers, lubricants, solvents, detergents, adhesives - all products; fuels that are used in most modern methods of transport (cars, trains, airplanes etc.)

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11
Q

what are petrol, diesel oil, kerosene, bitumen, heavy fuel oil and liquefied petroleum gases used for?

A

(respectively)
fuel for cars (gasoline); diesel engines (gas oil); jet fuel (paraffin); surfacing roads and roofs; ships and power stations; domestic heating and cooking

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12
Q

why does boiling point increase as we go down the alkanes?

A

molecules get larger; intermolecular forces of attraction between molecules becomes greater - more surface area contact between them; more energy is needed to separate the molecules

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13
Q

what is viscosity and what are the trends in hydrocarbons?

A

refers to the ease of flow of a liquid - high viscosity liquids = thick & flow less easily; increases with increasing chain length

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14
Q

what are the trends in flammability in hydrocarbons?

A

smaller hydrocarbon molecules are more flammable and are easier to ignite than larger molecules

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15
Q

what is produced in incomplete combustion?

A

insufficient oxygen = formation of carbon monoxide and water or carbon and water

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16
Q

why is carbon monoxide bad?

A

extremely poisonous gas - combines w haemoglobin in blood & prevents it from carrying oxygen; is colourless, odourless and tasteless, making it difficult to detect;
incomplete combustion occurs in some appliances e.g. boilers, stoves, and in internal combustion engines, where space is cramped

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17
Q

why is carbon that is produced from incomplete combustion bad?

A

causes respiratory problems; covers buildings and statues, making them look unclean; increases global dimming

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18
Q

what is an alkene? how is it different from an alkane, and why is it more desirable?

A

it has a carbon carbon double bond, making it unsaturated; more desirable as they are more reactive and can take part in reactions which alkanes cannot; can be used to make polymers, are the starting materials for the production of many other chemicals

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19
Q

what is cracking? what is produced?

A

process used to convert alkanes into short chain molecules which are more useful; alkenes and hydrogen are produced

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20
Q

what are the two methods for cracking? how do they work?

A

catalytic cracking and steam cracking
catalytic cracking: heat the hydrocarbon molecules to around 600 – 700°C to vaporise them; then pass the vapours over a hot powdered catalyst of aluminium oxide; this breaks covalent bonds in molecules as they come into contact with the surface of catalyst, causing thermal decomposition reactions; molecules are broken up in a random way which produces a mixture of smaller alkanes and alkenes; H and a higher proportion of alkenes are formed at temperatures of above 700ºC and higher pressure.
steam cracking: the same process is used; but the vaporised hydrocarbons are mixed with steam and heated to a high temperature which induces cracking.

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21
Q

what is the general formula for alkenes?

A

CnH2n

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22
Q

what is produced in the complete/incomplete combustion of alkenes?

A

complete: water & carbon dioxide;
incomplete: water & CO (always); CO2 or C

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23
Q

how can we test for alkenes?

A

add bromine water to the solution; it will go from orange to colourless

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24
Q

why are alkenes more reactive than alkanes?

A

double bond contains an area of high electron density; more bonds can be made w other atoms when double bond is opened

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25
Q

what is hydrogenation?

A

reaction w hydrogen to form an alkane; occur at 150ºC using a nickel catalyst; used to change vegetable oils into margarine to be sold in supermarkets

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26
Q

what is hydration?

A

reaction with steam to form an alcohol; used for production of alcohols; it occurs at temp. around 330ºC; pressure of 60 – 70 atm; needs a concentrated phosphoric acid catalyst; ethene is separated from ethanol and water easily - has a much lower boiling point; ethanol and water are separated afterwards by fractional distillation.

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27
Q

what is halogenation?

A

reactions with halogens; halogen atoms always add to the carbon atoms involved in the C=C double bond

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28
Q

what is the functional group of alkanes?

A

C-C

29
Q

what is the functional group of alkenes?

A

C=C

30
Q

what is the functional group of alcohols?

A

-OH

31
Q

what is the general formula for alcohols?

A

CnH2n+1OH

32
Q

what are the first four alcohols and their formulas?

A

methanol - CH3OH; ethanol - C2H5OH; propanol; - C3H7OH; butanol - C4H9OH

33
Q

what are the uses of alcohols?

A

alcoholic drink (ethanol); fuels - highly flammable; solvents (methanol and ethanol) - can dissolve many substances that water cannot e.g. fats and oils

34
Q

how can ethanol be produced by fermentation?

A

produced by fermentation where sugar or starch is dissolved in water and yeast is added; it is then fermented between 15 & 35°C with the absence of oxygen for a few days; yeast contains enzymes that break down starch or sugar to glucose; if temp. is too low reaction rate will be too slow and if it is too high enzymes will become denatured; yeast respires anaerobically using the glucose to form ethanol and carbon dioxide; yeast are killed off once the concentration of alcohol reaches around 15%, reaction vessel is emptied, process starts again - batch process.

35
Q

what is the reaction for the fermentation of sugar to produce ethanol?

A

C6H12O6 + Enzymes → 2CO2 + 2C2H5OH

36
Q

how can ethanol be produced by addition of steam to ethene?

A

a hydration process; C2H4 + H2O -> C2H5OH

37
Q

what are the advantages of using fermentation of sugar to produce ethanol?

A

sugar is renewable; it’s carbon neutral - absorbs CO2 as they grow

38
Q

what are the disadvantages of using fermentation of sugar to produce ethanol?

A

it’s a slow process; involves the destruction of habitats to grow plants; batch process; labour intensive; the result ethanol needs purifying

39
Q

what are the advantages of adding steam to ethene to produce ethanol?

A

produces pure ethanol w no waste products; fast process; less workers needed; continuous process

40
Q

what are the disadvantages of adding steam to ethene to produce ethanol?

A

ethene comes from crude oil - non-renewable; high temps are needed for reaction to take place so uses a lot of energy

41
Q

what are the trends in physical properties of alcohols?

A

w increased carbon chain length, boiling points increase, viscosity increases, solubility in water decreases - dissolve in water to form neutral solutions

42
Q

what is the balanced equation for the complete combustion of ethanol?

A

CH3CH2OH + 3O2 → 2CO2 + 3H2O

43
Q

.what is the balanced equation for the reaction of methanol with sodium?

A

2Na + 2CH3OH → 2CH3ONa + H2

fizzing, as hydrogen is produced

44
Q

how can you oxidise an alcohol?

A

warm it up with acidified potassium dichromate (an oxidising agent); they oxidise to form carboxylic acids; the potassium dichromate with turn from orange to green

45
Q

what is the equation for the oxidation of ethanol to produce ethanoic acid?

A

C2H5OH + O2 → CH3COOH + H2O

46
Q

what is the functional group of carboxylic acids?

A

-COOH

47
Q

what is the general formula for carboxylic acids?

A

CnH2n+ COOH

48
Q

what are the trends of physical properties of carboxylic acids like?

A

with increased carbon chain length, boiling points increase, viscosity increases

49
Q

what are the first four carboxylic acids?

A

methanoic acid - HCOOH, ethanoic acid - CH3COOH, propanoic acid - C2H5COOH, and butanoic acid C3H7COOH

50
Q

where is the double bond in carboxylic acids?

A

between the C=O(OH)

51
Q

what are the properties of carboxylic acids?

A

dissolve in water, partially ionise producing weakly acidic solutions; react w metals to form salt and hydrogen, w carbonates to form a salt, water and carbon dioxide gas; take part in neutralisation reactions w hydroxides to produce salt and water

52
Q

how do we name a salt made from carboxylic acid (+metal/carbonate)?

A

metal + –anoate

e.g. sodium ethanoate; magnesium methanoate

53
Q

how are esters formed?

A

by reacting carboxylic acids with alcohols; requires an acid catalyst -usually sulphuric acid; in this reaction, an ester and water are produced

54
Q

what is the functional group for an ester?

A

-COO-

55
Q

what can esters be used for?

A

they’re sweet smelling oily liquids used in food flavourings and perfumes.

56
Q

how is ethyl ethanoate produced? give the balanced symbol equation.

A

ethanoic acid + ethanol (w concentrated sulfuric acid) = ethyl ethanoate
CH3COOH + C2H5OH -> CH3COOC2H5 + H2O

57
Q

what are polymers?

A

large molecules made of repeating smaller molecules called monomers

58
Q

what is required for a polymerisation reaction?

A

high pressure, the use of a catalyst

59
Q

what are addition polymers?

A

formed by the joining up of many monomers and only occurs in monomers that contain C=C bonds (alkenes)

60
Q

what are condensation polymers?

A

formed by joining up monomers with two different function groups (don’t have to be C=C); a small molecule (usually water) is produced as a by product

61
Q

what are dicarboxylic acids?

A

a molecule w two carboxylic groups

62
Q

was are diols?

A

a molecule w two alcohol groups

63
Q

what happens when you react a dicarboxylic acid w a diol?

A

an ester link (-COO-) is formed; one molecule of water is lost

64
Q

how do you form a polyester?

A

react a dicarboxylic acid w a diol to form an ester (one molecule of water is lost); then repeat this unit (another molecule of water is lost - a H+ from the alcohol and a OH- from the acid)

65
Q

how are box diagrams drawn?

A

when drawing polymers, a box can be drawn to represent a hydrocarbon chain; other functional groups and links must be drawn clearly

66
Q

what are amino acids?

A

monomers which are used to make up protein polymers with 2 functional groups - NH2 (amine; basic) and COOH (carboxylic acid; acidic); bonds between amino acids are called peptide bonds - so they’re called polypeptides; one water molecule is lost per peptide link; proteins can have different amino acids in their chains; the order determines structure and properties

67
Q

what is the structure of DNA?

A

consists of four different monomers called nucleotides which contain small molecules called bases, which are bound together by polymerisation; nucleotides form two strands that intertwine, forming a double helix shape

68
Q

what is the structure of a nucleotide?

A

made up of three parts: a sugar molecule; a phosphate group; and a base

69
Q

what can monosaccharides (simple sugars) form?

A

starch; cellulose - complex carbohydrates called polysaccharides