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Worked solutions to textbook questions 1 Chapter 10 Organic reactions: pathways to new products Q1. Write balanced equations to represent the formation of all possible products of the reactions of chlorine with methane. A1. CH 4 (g) + Cl 2 (g) CH 3 Cl(g) + HCl(g) CH 3 Cl(g) + Cl 2 (g) CH 2 Cl 2 (g) + HCl(g) CH 2 Cl 2 (g) + Cl 2 (g) CHCl 3 (g) + HCl(g) CHCl 3 (g) + Cl 2 (g) CCl 4 (g) + HCl(g) Q2. Draw the structural formulas and name all the possible products that can be formed by the reaction of chlorine with ethane. Which substances are isomers? A2. Heinemann Chemistry 2 (4th edition) Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007
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Page 1: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 1

Chapter 10 Organic reactions: pathways to new products

Q1.

Write balanced equations to represent the formation of all possible products of the reactions of chlorine with methane.

A1.

CH4(g) + Cl2(g) CH3Cl(g) + HCl(g)CH3Cl(g) + Cl2(g) CH2Cl2(g) + HCl(g)CH2Cl2(g) + Cl2(g) CHCl3(g) + HCl(g)CHCl3(g) + Cl2(g) CCl4(g) + HCl(g)

Q2.

Draw the structural formulas and name all the possible products that can be formed by the reaction of chlorine with ethane. Which substances are isomers?

A2.

chloroethane: 1,1-dichloroethane; 1,2-dichloroethane; 1,1,1-trichloroethane1,1,2-trichloroethane: 1,1,1,2-tetrachloroethane; 1,1,2,2-tetrachloroethane1,1,1,2,2-pentachloroethane: hexachloroethaneIsomers are 1,1-dichloroethane and 1,2-dichloroethane1,1,1-trichloroethane and 1,1,2-trichloroethane

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 2: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 2

1,1,1,2-tetrachloroethane and 1,1,2,2-tetrachloroethane

Q3.

Name the products formed when propene reacts with:a hydrogen chloride (two possible products)b chlorinec water (two possible products)d hydrogen

A3.

a 1-chloropropane or 2-chloropropaneb 1,2-dichloropropanec propan-1-ol or propan-2-old propane

Q4.

Use structural formulas to write equations and name the products for the reactions of:a but-1-ene with chlorineb but-2-ene with hydrogen bromide (two possible products)

A4.

a

b

Q5.

Polyethenol is used to make soluble hospital laundry bags. The structure of the monomer ethenol is shown in Figure 10.9. Draw the structure of a section of the polymer.

Figure 10.9Structure of ethenol.

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 3: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 3

A5.

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 4: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 4

Q6.

Draw molecular structures and refer to the electronegativities given in the periodic table at the end of this book to work out whether each of the following substances has a dipole or is non-polar.a CH3Fb CH3CCl3

c CCl3CH2CCl3

A6.

a polarb polarc non-polar

Q7.

Write unbalanced equations for the production of:a methanol from chloromethaneb chloromethane from methanec propan-1-ol from 1-chloropropane

A7.

a CH3Cl(g) CH3OH(aq)b CH4(g) CH3Cl(g)c CH3CH2CH2Cl(l) CH3CH2CH2OH(l)

Q8.

Write a sequence of reactions that shows the production of:a ethanoic acid from ethaneb ethanoic acid from ethene

A8.

a CH3CH3(g) CH3CH2Cl(g) CH3CH2OH(aq) CH3COOH(aq)

b CH2CH2(g) CH3CH2OH(g) CH3COOH(aq)

Q9.

Label each step in Question 8 to show whether it is an addition, substitution or oxidation reaction.

A9.

a substitution, substitution, oxidation, oxidationb addition, oxidation, oxidation

Q10.

Write balanced equations for the reaction between ethanoic acid and:

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 5: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 5

a sodium hydroxide solutionb magnesium metalc sodium carbonate

A10.

a CH3COOH (aq) + NaOH (aq) CH3COONa (aq) + H2O(l)b 2CH3COOH (aq) + Mg (CH3COO)2Mg + H2O(l)c CH3COOH (aq) + Na2CO3(aq) 2CH3COONa (aq) + CO2(g) + H2O(l)

E1.

A condensation polymer used in medical sutures is made from glycolic acid monomer. The semi-structural formula of glycolic acid is HOCH2COOH.a What is meant by the term ‘condensation polymer’?b Name the functional groups present in glycolic acid.c Write an equation to represent the formation of a section of the polymer.d Draw the structural formula for a section of the polymer and circle the ester bond.

AE1.

a When condensation polymers are formed, small molecules such as water are eliminated when the monomer molecules combine.

b hydroxy,–OH and carboxy, –COOH functional groupsc, d

Q11.

Draw the structural formulas of the following esters and name them.a CH3COOCH3

b CH3COOCH2CH3

c CH3CH2COOCH2CH3

A11.

a

b

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 6: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 6

c

Q12.

Write equations that describe the formation of an ester to smell like:a pineapple (ethyl butanoate)b rum (ethyl methanoate)

A12.

a CH3CH2CH2COOH(l) + CH3CH2OH(l) CH3CH2CH2COOCH2CH3(l) + H2O(l)

b HCOOH(l) + CH3CH2OH(l) HCOOCH2CH3(l) + H2O(l)

Q13.

Devise reaction pathways for the following reactions:a ethylamine from etheneb butan-1-ol from butanec pentanoic acid from 1-chloropentane

A13.

a H2O NH3

Ethene ethanol ethylamineb Cl2 OH–

Butane 1-chlorobutane butan-1-olc OH– Cr2O7

2–, H+

1-chloropentane 1-pentanol pentanoic acid

Q14.

Name these esters and provide the systematic name of the alkanols and carboxylic acids used to form them.a CH3CH2CH2CH2COOCH3

b CH3CH2COOCH2CH2CH2CH2CH2CH3

A14.

a methyl pentanoate, from methanol and pentanoic acidb hexyl propanoate, from hexanol and propanoic acid

Q15.

Propose the shortest reaction pathway that will synthesise the following:

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 7: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 7

a methanoic acid from methaneb ethanol from ethenec propyl methanoate from propane and methane

A15.

a methane chloromethane methanol methanoic acidH2O

b ethene ethanolc This synthesis can be carried out in three stages: (i) synthesis of propan-1-ol,

(ii) synthesis of methanoic acid and (iii) synthesis of 1-propyl methanoateCl2 OH–

i propene 1-chloropropane propan-1-ol and Cl2 OH– Cr2O7

2–, H+

ii methane chloromethane methanol methanoic acid thenH+

iii propan-1-ol + methanoic acid 1-propyl methanoate + water

Q16.

Describe a reaction pathway to synthesise 1-butyl ethanoate using the appropriate alkanes or alkenes as starting materials.

A16.

This synthesis is carried out in three parts: (i). synthesis of 1 butanol, (ii) synthesis of ethanoic acid and (iii) synthesis of 1-butyl ethanoate.

Cl2 OH–

i butane 1-chlorobutane butan-1-olH2O Cr2O7

2–, H+

ii ethene ethanol ethanoic acidiii ethanoic acid + butan-1-ol 1-butyl ethanoate + water

Q17.

Calculate the percentage yield if 5.0 g of ethanol is oxidised to produce 4.8 g of ethanoic acid.

A17.Cr2O7

2–, H+

CH3CH2OH CH3COOHTheoretical yield (100% conversion of ethanol)

n(CH3COOH) = n(CH3CH2OH)

= mol

m(CH3COOH)= × 48 g = 5.2 g

% yield = × 100%

= × 100

= 92%

Q18.

Compound D can be synthesised using a reaction pathway that involves a number of intermediate steps. The yield for each step is shown.

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 8: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 8

A B C D

a Determine the overall yield for the preparation of compound D from compound A.

b How would the overall yield be affected if the yield for B C was only 10%?

A18.

a yield = 0.7 × 0.5 × 0.9 = 0.32; Yield = 32%b yield = 0.7 × 0.1 × 0.9 = 0.063; Yield = 6.3%

Q19.

Briefly describe the principles of fractional distillation.

A19.

In fractional distillation, the components of a mixture of volatile liquids are separated by what can be considered to be a succession of simple distillations. The temperature gradient in the fractionating column allows this to occur. Fractional distillation relies on the phenomena that the concentration of the low boiling point component in the vapour over a mixture of volatile liquids is higher than in the liquid.As the mixture of liquids is heated in the distillation flask, the vapours that move up the fractionating column contain a higher concentration of the more volatile liquid. The vapours eventually reach a height in the fractionating column where the temperature is low enough for condensation to occur. As the condensed liquid moves back down the column it is reheated by vapours rising from the distillation flask. Some of this condensed liquid evaporates and the resulting vapour has an even higher concentration of the low boiling point substance. This process of evaporation and condensation is repeated many times. The concentration of the more volatile substance increases in each evaporation–condensation cycle. Once the vapour reaches the top of the fractionating column it will ideally consist of only the more volatile component. When the relatively pure component reaches the top of the fractionating column, the temperature remains relatively stable. The material that condenses over a small temperature range near the boiling point is collected once it has passed through the condenser.

Q20.

Methane undergoes a series substitution reactions with bromine to form a number of compounds with the following boiling points: bromomethane (3.6°C), dibromomethane (97°C), tribromomethane (150°C), and tetrabromomethane (190°C). Describe how you would obtain pure samples of each compound from the mixture.

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 9: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 9

A20.

The mixture of volatile liquids can be separated by fractional distillation. The mixture is placed in the distillation flask and heated. The most volatile compound (bromomethane) is the first to reach the top of the fractionating column and condense. The fraction condensing in a narrow range of temperatures around the boiling point 3.6°C is collected. Because this temperature is below that of room temperature, the receiving flask should be surrounded by ice to condense the liquid bromomethane. The next fraction to be collected at around 97°C will contain dibromomethane. Tribromomethane will be found in the fraction collected at 150°C. Tetrabromomethane will found in the fraction collected at 190°C.

Chapter review

Q21.

Write unbalanced equations for the production of:a chloroethane from ethaneb ethanol from ethenec ethanol from chloroethaned ethanoic acid from ethanol

A21.

a CH3CH3(g) CH3CH2Cl(g)

b CH2CH2(g) CH3CH2OH(g)

c CH3CH2Cl(g) CH3CH2OH(aq)

d CH3CH2OH(aq) CH3COOH(aq)

Q22.

Classify the reactions in your answers to Question 21 as addition or substitution.

A22.

a substitutionb additionc substitutiond substitution

Q23.

Write the structural formulas of the products of the following reactions:a

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 10: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 10

b

c

d

A23.

a

b

c

d

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 11: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 11

Q24.

Write an unbalanced chemical equation for the reaction between:a butane and chlorineb 1-chlorobutane and sodium hydroxide solutionc butan-1-ol and acidified potassium dichromate solutiond propan-1-ol and acidified potassium permanganate solutione ethane and oxygen

A24.

a CH3CH2CH2CH3(g) CH3CH2CH2CH2Cl(l)b CH3CH2CH2CH2Cl(l) CH3CH2CH2CH2OH(aq)

c CH3CH2CH2CH2OH(aq) CH3CH2CH2COOH(aq)

d CH3CH2CH2OH(aq) CH3CH2COOH(aq)e 2C2H6(g) + 7O2(g) 4CO2(g) + 6H2O(g)

Q25.

Write chemical equations in the form of a flow diagram (similar to Figure 10.31) to describe the preparation of propanoic acid from: a an alkaneb an alkene

A25.

a

b

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 12: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 12

Q26.

Consider the following compounds:I

II

III

IV

V

a Write the names of each of these compounds.b Which of these compounds is a member of the alkane homologous series?c Give one important difference in chemical behaviour between compounds I

and V.d What important chemical is manufactured from compound II?e Which of these compounds dissolves in water to form an acidic solution?

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 13: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 13

A26.

a I methane, II chloroethane, III propane, IV ethanoic acid, V propeneb I, IIIc Compound V will decolourise bromine almost immediately, whereas compound I

will not. In general, compound I participates in substitution reactions (e.g. chlorination by chlorine gas to form chloromethane) whereas compound V participates in addition reactions (e.g. addition of HCl across the double bond to form chloropropane).

d ethanole IV

Q27.

Complete the following reactions:a

b

c

A27.

a CH3CH2COOCH3(l) + H2O(l) b CH3COO(CH2)4CH3(l) + H2O(l)c HCOOCH(CH3)2(l) + H2O(l)

Q28.

a Write a chemical equation to describe the preparation of propyl ethanoate from an alkanol and a carboxylic acid.

b What name is given to this type of reaction?c Sulfuric acid would be present in the reaction mixture. Why?

A28.

a CH3COOH(l) + CH3(CH2)2OH(l) CH3COO(CH2)2CH3(l) + H2O(l)b condensation and esterificationc catalyst

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 14: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 14

Q29.

Write reactions to show the production of:a methyl ethanoateb ethyl propanoate

A29.

a CH3COOH(l) + CH3OH(l) CH3COOCH3(l) + H2O(l)b CH3CH2COOH(l) + CH3CH2OH(l) CH3CH2COOCH2CH3(l) +

H2O(l)

Q30.

Write the formula of the alkanol and carboxylic acid used to make the following esters:a CH3COOCH2CH3

b CH3CH2COOCH2CH3

A30.

a CH3COOH, CH3CH2OHb CH3CH2COOH, CH3CH2OH

Q31.

In an experiment, the reaction of chlorine with ethane resulted in a mixture containing a number of products with the following boiling points: chloroethane (12°C), 1,1-dichloroethane (57°C), 1,2-dichloroethane (84°C), and 1,1,2-trichloroethane (97°C). Describe how you could obtain a pure sample of 1,2-dichloroethane from this mixture.

A31.

The mixture of volatile liquids can be separated by fractional distillation. The mixture is placed in the distillation flask and heated. The components in the mixture are separated in order of their boiling points with the most volatile component, chloroethane, being the first fraction to condense. This is followed by the fraction containing1,1-dichloroethane. The fraction condensing in a narrow range of temperatures around the boiling point of 1,2-dichlorethane, 84°C, is then collected in a new receiving flask.

Q32.

Complete the missing structural formula and name the reactant at points A, B and C.

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 15: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 15

A32.

A

B NaOH(aq)C

Q33.

Give the semi-structural formulas for substances P and Q and the systematic names for substances R and S in the following equation:

A33.

Formula P: CH3OHFormula Q: H2OSubstance R: propanoic acidSubstance S: methyl propanoate

Q34.

Write a reaction pathway for the synthesis of:a ethyl propanoate from ethene and propeneb ethyl ethanoate from an alkene

A34.

a Preparation of ethanol H2O

ethene ethanol

Synthesis of propanoic acid H2 Cl2 OH– Cr2O7

2–, H+

propene propane 1-chloropropane propan-1-ol propanoic acid Preparation of ethyl propanoate Ethanol + propanoic acid ethyl propanol + waterb Preparation of ethanol H2O

ethene ethanol Preparation of ethanoic acid

H2O Cr2O72–, H+

ethene ethanol ethanoic acid ethanol + ethanoic acid ethyl ethanoate + water

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007

Page 16: missballinger | Science and Mathematics Resources  · Web viewQ24. Write an unbalanced chemical equation for the reaction between: a butane and chlorine. b 1-chlorobutane and sodium

Worked solutions to textbook questions 16

Q35.

Fractional distillation is an important laboratory technique.a What is fractional distillation used for?b Fractional distillation has been described as a series of simple distillations.

Explain.

A35.

a Fractional distillation is used to separate liquids that have different boiling points. It is commonly used in the laboratory to separate volatile liquids from a reaction mixture. Industrial applications of fractional distillation include: Separation of the fractions from crude oil. Production of oxygen and nitrogen by the fractional distillation of liquid air. Extraction of ethanol from water in the fermentation of sugar.

b The mixture of liquids is heated in the distillation flask. The vapours that move up the fractionating column contain a higher concentration of the more volatile liquid. The vapours eventually reach a height in the fractionating column where the temperature is low enough for condensation to occur. As the condensed liquid moves back down the column it is reheated by vapours rising from the distillation flask. Some of this condensed liquid evaporates and the resulting vapour has an even higher concentration of the low boiling point substance. This process of evaporation and condensation is repeated many times. The concentration of the more volatile substance increases in each evaporation–condensation cycle. At the same time the concentration of the less volatile (higher boiling point) substance in the distillation flask will increase. Once the vapour reaches the top of the fractionating column it will ideally consist of only the most volatile component.

Heinemann Chemistry 2 (4th edition)Copyright © Pearson Education Australia (a division of Pearson Australia Group Pty Ltd) 2007