Topic 7 Organic Chemistry Flashcards

1
Q

What is the definition of a hydrocarbon?

A

A hydrocarbon is a compound that contains only hydrogen and carbon atoms.

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2
Q

T or F? Increasing the number of carbon atoms in an alkane will increase the viscosity.

A

True - alkanes with longer carbon chains are more viscous than those with shorter chains.

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3
Q

What is the molecular formula of the alkane that contains two carbon atoms?

A

C2H6 - the general formula of alkanes is CnH2n+2, which lets you work out the molecular formula of any alkane from the number of carbon (or hydrogen) atoms it contains.

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4
Q

S and J are taking about alkanes. j asks ‘what effect does molecular size have on the boiling point of alkanes?’. ‘It has no effect’ S replies. Is S correct? Explain your answer.

A

S is wrong. Smaller alkanes have lower boiling points (are more volatile) than larger alkanes, so the size of molecules in an alkane will affect the boiling point.

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5
Q

Under certain conditions pentane can undergo complete combustion. What’s the balanced symbol equation for the complete combustion of pentane (C5H12)?

A

C5H12 + 8O2 ⇒ 5CO2 + 6H2O

-complete combustion of a hydrocarbon always produces carbon dioxide (CO2) and water (H2O)

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6
Q

A scientist has a sample of butane (C4H10), decane (C10H22) and icosane (C20H42). She ignites the sample using a lighted splint. Which sample will be the hardest to ignite?

A

Icosane will the hardest to ignite. The ease of ignition of a hydrocarbon depends o its flammability, and the flammability of hydrocarbons decreases with increasing carbon carbon length. Therefore isocane will be the hardest to ignite, as its got the longest carbon chain and is the least flammable.

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7
Q

T or F? As a substance rises up a fractionating column, the temperature of the substance gradually increases?

A

False. The hottest part of the fractionating column is at the bottom, so substances cool down as the move up the column.

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8
Q

Crude oil is mainly formed from the remains of which type of organism?

A

Plankton - crude oil is formed from organisms that died millions of years ago and were buried in mud. Over time, high temperature and pressure turned their remains into oil.

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9
Q

Give some examples of fuels that can be produced from crude oil.

A

petrol, diesel, kerosene, heavy fuel oil, liquified petroleum gas (LPG)

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10
Q

A fractionating column is 50m tall. A certain fraction of crude oil, X, condenses at a height of 30m. Suggest why fraction X condensed at 30m.

A

The temperature of the fractioning column decreases as you move up the column. A fraction will only condense when it has reached part of the column that has a temperature below its boiling point. The temperature of the column at 30m must have been just below the boiling point of fraction X.

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11
Q

An oil refinery is carrying out fractional distillation of some crude oil. J wants to take a sample of crude oil that contains hydrocarbons with no more than 8 carbon atoms. Where in the fractionating column should J take her sample from? Explain your answer.

A

J should take her sample from near the top. Hydrocarbons with 8 carbon atoms are relatively short so will have lower boiling points than a lot of hydrocarbons in crude oil. This means that they condense near the top of the column, where its cooler. Hydrocarbons that contain more tan 8 carbon atoms will condense lower down the column, so J’s sample should contain mostly short-chain hydrocarbons if she collects it from near the top of the column.

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12
Q

Give one example of a fuel that is produced by the petrochemical industry, other than fuel.

A

solvents, lubricants, polymers, detergents

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13
Q

what are the conditions needed for steam cracking?

A

Steam cracking uses steam and very high temperatures.

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14
Q

3) Nonane (C₂H₂0) can be cracked to produce ethene (C₂H₂) and one other product. What’s the balanced symbol equation for this reaction?

A

3) C₂H20 → C₂H4 + C7H₁6 - there should be the same number of C and H atoms on both sides of any equations that show cracking. So you can find the formula of the unknown hydrocarbon by finding how many C and H atoms you need to keep both sides balanced. (Hopefully this sounds vaguely familiar it’s basically just the law of conservation of mass, but applied to cracking.)

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15
Q

4) A company wants to use cracking to make petrol. The compounds in petrol contain ~8 carbon atoms.
Look at the table below. How suitable are each of the fractions for cracking to make petrol? Which would be the best choice for the company?

A

4) The compounds in LPG contain roughly three carbon atoms, so are too short to be cracked to make petrol (which contains compounds with around eight carbon atoms). Kerosene and bitumen both contain hydrocarbons that are long enough to be cracked to make petrol. Bitumen is in lower demand than kerosene, so isn’t as useful. Therefore bitumen is the best choice to be cracked to make petrol.

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16
Q

1) What’s the name of the first member of the alkene homologous series?

A

1) Ethene — the names of the next three members are propene, butene and pentene.

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17
Q

2) An alkene contains 7 carbon atoms. How many hydrogen atoms will it have?

A

2) 14 hydrogen atoms the general formula for alkenes is CH₁ so a molecule of any alkene will always contain twice as many H atoms as C atoms.

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18
Q

3)
A scientist finds a bottle of liquid in the lab. Unfortunately, the label on the bottle
is a bit damaged, so the scientist can’t tell if it contains pentane or pentene. The scientist burns the sample in air, and records his observations. How could the scientist use his results to distinguish between the two compounds?

A

3) If the scientist sees a smoky yellow flame, he can be fairly sure that the compound is pentene. Alkenes burn cleanly in plenty of oxygen, just like other hydrocarbons such as pentane. But in air, where there isn’t quite as much oxygen, alkenes tend to undergo incomplete combustion. This is why a smoky flame is produced.

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19
Q

Mishal is investigating the combustion reactions of alkenes. She starts by burning a sample of propene in a high level of oxygen. She repeats the reaction with a fresh sample of propene, but in a low level of oxygen.
Describe the products that you would expect each reaction to form.
Give reasons for your answer.

A

4) In high levels of oxygen, propene will combust completely to produce carbon dioxide and water (and release some energy). But when Mishal repeats the reaction in a low level of oxygen, propene will undergo incomplete combustion. This reaction will produce carbon dioxide and water (just like complete combustion), but will also produce at least one of carbon monoxide and carbon/soot.

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20
Q

1) What happens to the C=C bond in an alkene when it reacts with H₂?

A

1)
When an alkene reacts with H₂, one H atom adds to each C atom in the C=C This causes the double bond to break and turn in to C-C single bond.

21
Q

2) Why are the reactions of ethene very similar to those of propene?

A

2) In general, it’s the functional group that determines how a molecule reacts.
Ethene and propene both contain the C=C functional group, so react in very similar ways.

22
Q

Use the structures, A-D, on the right to help you answer questions 3-5.

3) which of A-C would be formed if a hydrocarbon containing a C=C bond was reacted with H2?
4) Which alkene would react with Cl₂ to make A?
5) What are the reactants and conditions for converting ethene into D? 6) Genevieve has a sample of hexene (C₂H₁₂).
Describe how she could use bromine water to confirm that the sample is an alkene.
What would be the molecular formula of the organic product formed during the test?

A

3) B - this compound is ethane, which would form if ethene was reacted with hydrogen.
4) Butene the Cl atoms would add across the C=C double bond in butene. 5) H₂O/steam and a catalyst - these conditions will convert an alkene into an
alcohol.
You can tell that compound D is an alcohol because it contains an -OH functional group.
6) Add bromine water to the sample, and shake. If the solution turns from orange to colourless, the sample contains the alkene functional group (which indicates that the sample could be hexene). The bromine atoms would add across the double bond in hexene, to form a product with the molecular formula C₂H₁₂Br₂.

23
Q

1) Give the two-word name of the type of reaction that occurs

A

1) Addition polymerisation - lots of alkene monomers “add”
together, forming a polymer.

24
Q

2) How many products are formed when propene monomers react with each other?

A

2) Propene monomers only react to form one product poly(propene). In fact, addition
polymerisation always produces one product, no matter what the monomers are.

25
Q

3) What does the little “n” represent in the formula of an addition polymer?

A

3) The little “n” stands for any number.
It tells you that the monomer unit is repeated lots of times.

26
Q

4) Suggest the name of the polymer that forms from fluoroethene (C₂H₂F) monomers.

A

4) Fluoroethene monomers form poly(fluoroethene). To name a polymer, just put the name of the monomer in brackets and put “poly” on the front.

27
Q

5) The formula of a polymer is shown on the right.
Give the name of the monomer that forms this polymer.

A

5) Ethene - you can work out the formula of a monomer by counting the number of atoms of each type in the repeating unit. There are 2 C atoms and 4 H atoms in the repeating unit of this polymer, so the monomer that made it has the formula C₂H₂, which is ethene.

28
Q

6) How do you draw the displayed formula of an addition polymer
from the displayed formula of its monomer?

A

6) Draw the two carbon atoms that make up the alkene double bond, but replace the double bond with a single bond. Add a single bond to either side of the two carbon atoms. Fill in the rest of the groups, in the same way that they are bonded to the double bond in the
monomer. Draw a pair of brackets around the repeat unit (make sure the bonds either side of the carbon atoms are sticking out of the brackets), and put a little “n” after.

29
Q

1) What’s the name of the first member of the alcohol homologous series?

A

Methanol (CH3OH) is the first member of the alcohol homologous series.

30
Q

2) Name the two products formed in the complete combustion of alcohol

A

Water and carbon dioxide. alcohols are reactive so normally combust completely in air.

31
Q

3) Give two uses of alcohols.

A

Alcohols are used as industrial solvents. They are also used as fuels.

32
Q

4) A scientist has a sample of alcohol X. She finds that alcohol X contains two more carbon atoms than propanol. What’s the molecular formula of alcohol X?

A

Propanol contains 3 carbon atoms (it has a molecular formula C3H7OH), also alcohol X must contain 5 carbon atoms. Each member of the homologous series of alcohols contains one more -CH2 group than the previous member. So adding two carbon atoms to an alcohol will add 4 extra hydrogen atoms to its molecular formula. So alcohol X must have the molecular formula C5H11OH/ C5H12O

33
Q

5) Potassium permanganate (KMnO4) is a strong dising agent. Suggest what would happen if some KMnO4, was added to propanol.

A

Oxidising agents are substances that can be used to oxidise other substances. Alcohols are oxidised to produce carboxylic acids, so propanol would be oxidides to propanoic acid.

34
Q

6) Describe the optimal conditions for the fermentation of sugar using yeast. Name the alcohol formed during the process.

A

The optimal conditions for fermentation using yeast are a warm temperature (around 37°C) in a slightly acidic solution under aerobic conditions/ without an oxygen present. (These are the conditions at which the enzyme in yeast works best.) The fermentation of suger produces ethanol.

35
Q

1) What is the formula of the functional group in carboxylic acids?

A

-COOH -all carboxylic acids contain this functional group

36
Q

2) How many carbon atoms are there in a molecule of methanoic acid?

A

2) A molecule of methanoic acid contains one carbon atom (it’s got the formula HCOOH).

37
Q

3) What is the molecular formula of butanoic acid?

A

3) C3H7COOH/C4H8O₂-butanoic acid is the fourth member of the carboxylic acid
homologous series, after methanoic, ethanoic and propanoic acids.

38
Q

4) A student adds a spatula of calcium carbonate to methanoic acid. Give the word equation for the reaction that takes place.

A

4) methanoic acid + calcium carbonate → calcium methanoate + water + carbon

39
Q

5) A scientist reacts ethanoic acid with ethanol in the presence of an acid catalyst. Name the organic product formed during the reaction.

A

5) Ethyl ethanoate - carboxylic acids react with alcohols to form esters.
Thankfully, ethyl ethanoate the only ester that you need to know the name of.

40
Q

6) Anita pours 250 cm³ of water into each of two flasks, labelled A and B. She dissolves 0.1 moles of ethanoic acid in flask A, and 0.1 moles of HCI in flask B. HCI is a strong acid. Anita finds that the solution in flask A has a pH of 2.6, and the solution in flask B has a pH of 0.4. Explain Anita’s results.

A

6) The HCI solution has a lower pH than the ethanoic acid solution because HCI is a strong acid, and ethanoic acid is a weak acid. This means that ethanoic acid doesn’t ionise completely in solution/not all of the ethanoic acid molecules release their H+ ions (whereas HCI does). Because of this, the concentration of H+ ions in the ethanoic acid solution will be lower than in the HCI solution, so ethanoic acid solution is less acidic.

41
Q

1) Give an example of a small molecule that is lost during a condensation polymerisation reaction.

A

1) e.g. water/H₂O

42
Q

2) What type of condensation polymer is formed when monomer containing two -OH groups reacts with a monomer containing two -COOH groups?

A

2) A polyester. The reaction between an alcohol (-OH) and a carboxylic acid (-COOH)
produces an ester. So the reaction between a monomer containing two -OH groups and a monomer containing two -COOH groups will produce a polyester.

43
Q

3) Lactic acid, shown on the right, can undergo self-polymerisation. Self-polymerisation occurs when a condensation polymer forms from only one type of monomer. Suggest why
lactic acid can undergo a self-polymerisation reaction.

A

3) Lactic acid contains two different functional groups an alcohol group and a carboxylic acid group. The carboxylic acid group from one lactic acid molecule can react with the alcohol group from another lactic acid molecule, forming an ester bond. More lactic acid molecules can react with the other functional groups in this ester, forming a polyester.

44
Q

4) The repeating unit of condensation polymer G is shown on the right. Polymer G is made from two monomers, X and Y. Monomer X has the molecular formula HOC₂H₂OH. Suggest the molecular formula of monomer Y.

A

4) C3H4O4/HOOCCH₂COOH-G has an ester bond, so it’s a polyester. Polyesters form from monomers with alcohol and carboxylic acid functional groups. Monomer X has two -OH groups, so monomer must be a carboxylic acid. You can work out the formula of the carboxylic acid monomer by looking at either side of the C-O in the ester bond. The part of the chain with the C=O bond comes from the carboxylic acid monomer.

45
Q

1) What functional groups do amino acids always have?

A

Amino acids always contain an amino/amine group (NH2) and a carboxyl group (COOH)

46
Q

2) True or False? Starch is a naturally occurring polymer made up of amino acids.

A

False - starch is a polmer made up of simple sugars

47
Q

3) Ella is investigating the naturally occurring polymers that make up plant cell walls. She starts by extracting the cellulose from samples of plant cells. Ella then boils the resulting mixture, in order to break the bonds between the monomers in the cellulose.
What type of monomers will be formed during this process?

A

Simple sugars will be produced - these are the monomers that make up cellelose.

48
Q

4) DNA is a naturally occurring polymer made up of monomers called nucleotides.
Describe the structure of DNA.

A

DNA is made up of two polymer chains. Each chain is made of nucleotides bonded together. The DNA chains bond to each other to form a double helix structure.

49
Q

5) A scientist adds samples of three different amino acids to a conical flask containing some water and leaves it in a warm place for a couple of weeks. When she comes back, she finds that a small amount of a polymer has formed from the amino acids. What is the name given to polymers made up of amino acids? How do they form?

A

Amino acids form condensation polymers called polypeptides. Amino acids can form these polymers as they contain two different functional groups that can react with each other. The amine/NH2 group of one amino acid reacts with the carboxyl/COOH group of another amino acid. For every bond that is formed a molecule of water is lost. (This is how a polyester forms)