Define the term first ionization energy.

Explain why the first ionization energy of magnesium is higher than that of sodium.

calcium has a higher melting point than potassium.

sodium oxide has a higher melting point than sulfur trioxide.

Define the terms acid and base according to the Brønsted-Lowry theory and state one example of a weak acid and one example of a strong base.

Describe two different methods, one chemical and one physical, other than measuring the pH, that could be used to distinguish between ethanoic acid and hydrochloric acid solutions of the same concentration.

Black coffee has a pH of 5 and toothpaste has a pH of 8. Identify which is more acidic and deduce how many times the \({\text{[}}{{\text{H}}^ + }{\text{]}}\) is greater in the more acidic product.

Samples of sodium oxide and sulfur trioxide are added to separate beakers of water. Deduce the equation for each reaction and identify each oxide as acidic, basic or neutral.

Draw the Lewis structure for chloroethene and predict the H–C–Cl bond angle.

Draw a section of poly(chloroethene) containing six carbon atoms.

Outline why the polymerization of alkenes is of economic importance and why the disposal of plastics is a problem.

Chloroethene can be converted to ethanol in two steps. For each step deduce an overall equation for the reaction taking place.

Step 1:

Step 2:

State the reagents and conditions necessary to prepare ethanoic acid from ethanol in the laboratory.

State an equation, including state symbols, for the reaction of ethanoic acid with water. Identify a Brønsted-Lowry acid in the equation and its conjugate base.

(i)     Use the graph to deduce whether the forward reaction is exothermic or endothermic and explain your choice.

(ii)     State and explain the effect of increasing the pressure on the yield of ammonia.

(iii)     Explain the effect of increasing the temperature on the rate of reaction.

(i)     Define oxidation in terms of oxidation numbers.

(ii)     Deduce the oxidation states of nitrogen in the nitrate, \({\text{NO}}_{\text{3}}^ - \), and nitrite, \({\text{NO}}_{\text{2}}^ - \), ions.

The nitrite ion is present in nitrous acid, HNO₂, which is a weak acid. The nitrate ion is present in nitric acid, HNO₃, which is a strong acid. Distinguish between the terms strong and weak acid and state the equations used to show the dissociation of each acid in aqueous solution.

A small piece of magnesium ribbon is added to solutions of nitric and nitrous acid of the same concentration at the same temperature. Describe two observations that would allow you to distinguish between the two acids.

(i)     Calculate the volume of the sodium hydroxide solution required to react exactly with a \({\text{15.0 c}}{{\text{m}}^{\text{3}}}\) solution of \({\text{0.10 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) nitric acid.

(ii)     The following hypothesis was suggested by the student: “Since nitrous acid is a weak acid it will react with a smaller volume of the \({\text{0.20 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) sodium hydroxide solution.” Comment on whether or not this is a valid hypothesis.

The graph below shows how the conductivity of the two acids changes with concentration.

Identify Acid 1 and explain your choice.

Nitric acid reacts with silver in a redox reaction.

__ \({\text{Ag(s)}} + \) __ \({\text{NO}}_3^ - {\text{(aq)}} + \) ___ \( \to \) ___\({\text{A}}{{\text{g}}^ + }{\text{(aq)}} + \) __ \({\text{NO(g)}} + \) ____

Using oxidation numbers, deduce the complete balanced equation for the reaction showing all the reactants and products.

(i)     Define oxidation and reduction in terms of electron loss or gain.

Oxidation:

Reduction:

(ii)     Deduce the oxidation numbers of arsenic and nitrogen in each of the following species.

\({\text{A}}{{\text{s}}_{\text{2}}}{{\text{O}}_{\text{3}}}\):

\({\text{NO}}_3^ - \):

\({{\text{H}}_{\text{3}}}{\text{As}}{{\text{O}}_{\text{3}}}\):

\({{\text{N}}_{\text{2}}}{{\text{O}}_{\text{3}}}\):

(iii)     Distinguish between the terms oxidizing agent and reducing agent.

(iv)     In the removal of arsenic from contaminated groundwater, \({{\text{H}}_{\text{3}}}{\text{As}}{{\text{O}}_{\text{3}}}\) is often first oxidized to arsenic acid, \({{\text{H}}_{\text{3}}}{\text{As}}{{\text{O}}_{\text{4}}}\).

The following unbalanced redox reaction shows another method of forming \({{\text{H}}_{\text{3}}}{\text{As}}{{\text{O}}_{\text{4}}}\).

\[{\text{A}}{{\text{s}}_2}{{\text{O}}_3}{\text{(s)}} + {\text{NO}}_3^ - {\text{(aq)}} \to {{\text{H}}_3}{\text{As}}{{\text{O}}_4}{\text{(aq)}} + {{\text{N}}_2}{{\text{O}}_3}{\text{(aq)}}\]

Deduce the balanced redox equation in acid, and then identify both the oxidizing and reducing agents.

Define an acid according to the Brønsted–Lowry and Lewis theories.

Brønsted–Lowry theory:

Lewis theory:

The Lewis (electron dot) structure of nitrous acid is given below.

Identify which nitrogen-oxygen bond is the shorter.

Deduce the approximate value of the hydrogen-oxygen-nitrogen bond angle in nitrous acid and explain your answer.

Distinguish between a strong acid and a weak acid in terms of their dissociation in aqueous solution.

Ammonia, NH₃, is a weak base. Deduce the Lewis (electron dot) structure of NH₃. State the name of the shape of the molecule and explain why NH₃ is a polar molecule.

When lime was added to a sample of soil, the pH changed from 5 to 7. Calculate the factor by which the hydrogen ion concentration changes.

One common nitrogen-containing fertilizer is ammonium sulfate. State its chemical formula.

Distinguish between the terms strong base and weak base, and state one example of each.

State the equation for the reaction of ammonia with water.

Explain why ammonia can act as a Brønsted–Lowry base.

Explain why ammonia can also act as a Lewis base.

(i)     When ammonium chloride, \({\text{N}}{{\text{H}}_{\text{4}}}{\text{Cl(aq)}}\), is added to excess solid sodium carbonate, \({\text{N}}{{\text{a}}_{\text{2}}}{\text{C}}{{\text{O}}_{\text{3}}}{\text{(s)}}\), an acid–base reaction occurs. Bubbles of gas are produced and the solid sodium carbonate decreases in mass. State one difference which would be observed if nitric acid, \({\text{HN}}{{\text{O}}_{\text{3}}}{\text{(aq)}}\), was used instead of ammonium chloride.

(ii)     Deduce the Lewis structures of the ammonium ion, \({\text{NH}}_4^ + \), and the carbonate ion, \({\text{CO}}_3^{2 - }\).

Ammonium ion\(\quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \quad \)Carbonate ion

(iii)     Predict the shapes of \({\text{NH}}_4^ + \) and \({\text{CO}}_3^{2 - }\).

\({\text{NH}}_4^ + \):

\({\text{CO}}_3^{2 - }\):

(i)     Sketch and label an enthalpy level diagram for this reaction.

(ii)     Deduce whether the reactants or the products are more energetically stable, stating your reasoning.

(iii)     Calculate the change in heat energy, in kJ, when \({\text{50.0 c}}{{\text{m}}^{\text{3}}}\) of \({\text{2.50 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) sodium hydroxide solution is added to excess nitric acid.

When 5.35 g ammonium chloride, \({\text{N}}{{\text{H}}_{\text{4}}}{\text{Cl(s)}}\), is added to \({\text{100.0 c}}{{\text{m}}^{\text{3}}}\) of water, the temperature of the water decreases from 19.30 °C to 15.80 °C. Determine the enthalpy change, in \({\text{kJ}}\,{\text{mo}}{{\text{l}}^{ - 1}}\), for the dissolving of ammonium chloride in water.

Draw the Lewis structures for carbon monoxide, CO, carbon dioxide, \({\text{C}}{{\text{O}}_{\text{2}}}\) and methanol, \({\text{C}}{{\text{H}}_{\text{3}}}{\text{OH}}\).

List, with an explanation, the three compounds in order of increasing carbon to oxygen bond length (shortest first).

\({\text{C}}{{\text{O}}_{\text{2}}}\)

\({\text{CO}}_3^{2 - }\)

\({\text{BF}}_4^ - \)

Define a Brønsted-Lowry acid.

Deduce the two acids and their conjugate bases in the following reaction:

\[{{\text{H}}_2}{\text{O(l)}} + {\text{N}}{{\text{H}}_3}{\text{(aq)}} \rightleftharpoons {\text{O}}{{\text{H}}^ - }{\text{(aq)}} + {\text{NH}}_4^ + {\text{(aq)}}\]

Define the term weak acid and state the equation for the reaction of ethanoic acid with water.

Vinegar, which contains ethanoic acid, can be used to clean deposits of calcium carbonate from the elements of electric kettles. State the equation for the reaction of ethanoic acid with calcium carbonate.

(i) Draw a Lewis (electron dot) structure of phosphine.

(ii) Outline whether you expect the bonds in phosphine to be polar or non-polar, giving a brief reason.

(iii) Explain why the phosphine molecule is not planar.

(iv) Phosphine has a much greater molar mass than ammonia. Explain why phosphine has a significantly lower boiling point than ammonia.

Phosphine is usually prepared by heating white phosphorus, one of the allotropes of phosphorus, with concentrated aqueous sodium hydroxide. The equation for the reaction is:

P4 (s) + 3OH⁻ (aq) + 3H₂O (l) → PH₃ (g) + 3H₂PO₂⁻ (aq)

(i) Identify one other element that has allotropes and list two of its allotropes.

Element:

Allotrope 1:

Allotrope 2:

(ii) The first reagent is written as P₄, not 4P. Describe the difference between P₄ and 4P.

(iii) The ion H₂PO₂⁻ is amphiprotic. Outline what is meant by amphiprotic, giving the formulas of both species it is converted to when it behaves in this manner.

(iv) State the oxidation state of phosphorus in P₄ and H₂PO₂⁻.

P₄:

H₂PO₂⁻:

(v) Oxidation is now defined in terms of change of oxidation number. Explore how earlier definitions of oxidation and reduction may have led to conflicting answers for the conversion of P₄ to H₂PO₂⁻ and the way in which the use of oxidation numbers has resolved this.

2.478 g of white phosphorus was used to make phosphine according to the equation:

P₄(s) +3OH⁻(aq)+3H₂O(l) → PH₃(g)+3H₂PO₂⁻(aq)

(i) Calculate the amount, in mol, of white phosphorus used.

(ii) This phosphorus was reacted with 100.0 cm³ of 5.00 mol dm⁻³ aqueous sodium hydroxide. Deduce, showing your working, which was the limiting reagent.

(iii) Determine the excess amount, in mol, of the other reagent.

(iv) Determine the volume of phosphine, measured in cm³ at standard temperature and pressure, that was produced.

Deduce the change in hydrogen ion concentration, \({\text{[}}{{\text{H}}^ + }{\text{]}}\).

State the name of the compound formed that is responsible for this decreased pH value.

Sulfuric acid present in acid rain can damage buildings made of limestone. Predict the balanced chemical equation for the reaction between limestone and sulfuric acid including state symbols.

State the names of the three organic functional groups in aspirin.

Determine the amount, in mol, of salicylic acid, \({{\text{C}}_{\text{6}}}{{\text{H}}_{\text{4}}}{\text{(OH)COOH}}\), used.

Calculate the theoretical yield, in g, of aspirin, \({{\text{C}}_{\text{6}}}{{\text{H}}_{\text{4}}}{\text{(OCOC}}{{\text{H}}_{\text{3}}}{\text{)COOH}}\).

Determine the percentage yield of pure aspirin.

State the number of significant figures associated with the mass of pure aspirin obtained, and calculate the percentage uncertainty associated with this mass.

Another student repeated the experiment and obtained an experimental yield of 150%. The teacher checked the calculations and found no errors. Comment on the result.

The following is a three-dimensional computer-generated representation of aspirin.

A third student measured selected bond lengths in aspirin, using this computer program and reported the following data.

The following hypothesis was suggested by the student: “Since all the measured carbon-carbon bond lengths are equal, all the carbon-oxygen bond lengths must also be equal in aspirin. Therefore, the C8–O4 bond length must be 1.4 \( \times \) 10^–10 m”. Comment on whether or not this is a valid hypothesis.

The other product of the reaction is ethanoic acid, \({\text{C}}{{\text{H}}_{\text{3}}}{\text{COOH}}\). Define an acid according to the Brønsted-Lowry theory and state the conjugate base of \({\text{C}}{{\text{H}}_{\text{3}}}{\text{COOH}}\).

Brønsted-Lowry definition of an acid:

Conjugate base of \({\text{C}}{{\text{H}}_{\text{3}}}{\text{COOH}}\):

Identify the boiling points for each of the isomers A, B and C and state a reason for your answer.

State the IUPAC names of isomers B and C.

B:

C:

Both \({{\text{C}}_{\text{5}}}{{\text{H}}_{{\text{12}}}}\) and \({{\text{C}}_{\text{5}}}{{\text{H}}_{{\text{11}}}}{\text{OH}}\) can be used as fuels. Predict which compound would release a greater amount of heat per gram when it undergoes complete combustion. Suggest two reasons to support your prediction.

In many cities around the world, public transport vehicles use diesel, a liquid hydrocarbon fuel, which often contains sulfur impurities and undergoes incomplete combustion. All public transport vehicles in New Delhi, India, have been converted to use compressed natural gas (CNG) as fuel. Suggest two ways in which this improves air quality, giving a reason for your answer.

State the initial and final oxidation numbers of titanium and hence deduce whether it is oxidized or reduced in this change.

Considering the above equilibrium, predict, giving a reason, how adding more acid would affect the strength of the \({\text{Ti}}{{\text{O}}^{2 + }}\) ion as an oxidizing agent.

Deduce which of the species would react with titanium metal.

Deduce the balanced equation for this reaction.

Deduce which of the six species is the strongest oxidizing agent.

A voltaic cell can be constructed using cadmium and europium half-cells. State how the two solutions involved should be connected and outline how this connection works.

Define a Brønsted–Lowry acid.

Distinguish between the terms strong acid and weak acid.

Neelu and Charles decided to solve the problem by determining the volume of \({\text{0.100 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) sodium hydroxide solution needed to neutralize \({\text{25.0 c}}{{\text{m}}^{\text{3}}}\) of the acid. Outline whether this was a good choice.

Neelu and Charles decided to compare the volume of sodium hydroxide solution needed with those required by known \({\text{0.100 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) strong and weak acids. Unfortunately they chose sulfuric acid as the strong acid. Outline why this was an unsuitable choice.

State a suitable choice for both the strong acid and the weak acid.

Strong acid:

Weak acid:

Francisco and Shamiso decided to measure the pH of the initial solution, HQ, and they found that its pH was 3.7. Deduce, giving a reason, the strength (weak or strong) of the acid HQ.

Suggest a method, other than those mentioned above, that could be used to solve the problem and outline how the results would distinguish between a strong acid and a weak acid.

Describe the acid-base character of the oxides of each of the period 3 elements, Na to Cl.

State one example of an acidic gas, produced by an industrial process or the internal combustion engine, which can cause large-scale pollution to lakes and forests.

Suggest one method, other than measuring pH, which could be used to distinguish between solutions of a strong acid and a weak acid of the same molar concentration. State the expected results.

(i)     The graph shows the volume of hydrogen produced against time under these experimental conditions.

Sketch two curves, labelled I and II, to show how the volume of hydrogen produced (under the same temperature and pressure) changes with time when:

I.     using the same mass of magnesium powder instead of a piece of magnesium ribbon;

II.     0.100 g of magnesium ribbon is added to \({\text{50 c}}{{\text{m}}^{\text{3}}}\) of \({\text{0.500 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) sulfuric acid.

(ii)     Outline why it is better to measure the volume of hydrogen produced against time rather than the loss of mass of reactants against time.

(i)     Calculate the amount, in mol, of anhydrous magnesium sulfate.

(ii) Calculate the enthalpy change, \(\Delta {H_1}\), for anhydrous magnesium sulfate dissolving in water, in \({\text{kJ}}\,{\text{mo}}{{\text{l}}^{ - 1}}\). State your answer to the correct number of significant figures.

(i)     Determine the enthalpy change, \(\Delta H\), in \({\text{kJ}}\,{\text{mo}}{{\text{l}}^{ - 1}}\), for the hydration of solid anhydrous magnesium sulfate, \({\text{MgS}}{{\text{O}}_{\text{4}}}\).

(ii)     The literature value for the enthalpy of hydration of anhydrous magnesium sulfate is \( - 103{\text{ kJ}}\,{\text{mo}}{{\text{l}}^{ - 1}}\). Calculate the percentage difference between the literature value and the value determined from experimental results, giving your answer to one decimal place. (If you did not obtain an answer for the experimental value in (c)(i) then use the value of \( - 100{\text{ kJ}}\,{\text{mo}}{{\text{l}}^{ - 1}}\), but this is not the correct value.)

Another group of students experimentally determined an enthalpy of hydration of \( - 95{\text{ kJ}}\,{\text{mo}}{{\text{l}}^{ - 1}}\). Outline two reasons which may explain the variation between the experimental and literature values.

(i)     State the equation for the reaction of sulfuric acid with magnesium carbonate.

(ii)     Deduce the Lewis (electron dot) structure of the carbonate ion, giving the shape and the oxygen-carbon-oxygen bond angle.

Lewis (electron dot) structure:

Shape:

Bond angle:

Calculate the relative atomic mass of this sample of magnesium correct to two decimal places.

Predict the relative atomic radii of the three magnesium isotopes, giving your reasons.

Describe the bonding in magnesium.

State an equation for the reaction of magnesium oxide with water.

A student added 5.00 g of \({{\text{P}}_{\text{4}}}{{\text{O}}_{{\text{10}}}}\) to 1.50 g of water. Determine the limiting reactant, showing your working.

Calculate the mass of phosphoric(V) acid, \({{\text{H}}_{\text{3}}}{\text{P}}{{\text{O}}_{\text{4}}}\), formed in the reaction.

State a balanced equation for the reaction of aqueous \({{\text{H}}_{\text{3}}}{\text{P}}{{\text{O}}_{\text{4}}}\) with excess aqueous sodium hydroxide, including state symbols.

State the formula of the conjugate base of \({{\text{H}}_{\text{3}}}{\text{P}}{{\text{O}}_{\text{4}}}\).

(i)     Deduce the Lewis structure of \({\text{PH}}_4^ + \).

(ii)     Predict, giving a reason, the bond angle around the phosphorus atom in \({\text{PH}}_4^ + \).

(iii)     Predict whether or not the P–H bond is polar, giving a reason for your choice.

Use the data in the table to identify the most acidic water sample.

Calculate the percentage uncertainty in the measured pH of the rain water sample.

Determine the ratio of \({\text{[}}{{\text{H}}^ + }{\text{]}}\) in bottled water to that in rain water.

\[\frac{{[{H^ + }]{\text{ }}in{\text{ }}bottled{\text{ }}water}}{{[{H^ + }]{\text{ }}in{\text{ }}rain{\text{ }}water}}\]

The acidity of non-polluted rain water is caused by dissolved carbon dioxide. State an equation for the reaction of carbon dioxide with water.

For each of the reactions A and B, deduce whether water is acting as an acid or a base and explain your answer.

In reaction B, identify the stronger base, \({\text{NH}}_2^ - \) or \({\text{O}}{{\text{H}}^ - }\) and explain your answer.

In reactions A and B, identify the stronger acid, \({\text{NH}}_4^ + \) or \({\text{N}}{{\text{H}}_{\text{3}}}\) (underlined) and explain your answer.

Describe two different experimental methods to distinguish between aqueous solutions of a strong base and a weak base.

Calculate the hydrogen ion concentrations in the two solutions and identify the stronger acid.

Determine the ratio of the hydrogen ion concentrations in the two solutions X and Y.

Distinguish between a weak acid and a strong acid.

Weak acid:

Strong acid:

Suggest why it is more convenient to express acidity using the pH scale instead of using the concentration of hydrogen ions.

5.00 g of an impure sample of hydrated ethanedioic acid, (COOH)₂•2H₂O, was dissolved in water to make 1.00 dm³ of solution. 25.0 cm³ samples of this solution were titrated against a 0.100 mol dm^-3 solution of sodium hydroxide using a suitable indicator.

(COOH)₂ (aq) + 2NaOH (aq) → (COONa)₂ (aq) + 2H₂O (l)

The mean value of the titre was 14.0 cm³.

(i)   Calculate the amount, in mol, of NaOH in 14.0 cm³ of 0.100 mol dm^-3 solution.

(ii)  Calculate the amount, in mol, of ethanedioic acid in each 25.0 cm³ sample.

(iii) Determine the percentage purity of the hydrated ethanedioic acid sample.

The Lewis (electron dot) structure of the ethanedioate ion is shown below.

Outline why all the C–O bond lengths in the ethanedioate ion are the same length and suggest a value for them. Use section 10 of the data booklet.

(i)     Describe the colour change that occurs when aqueous chlorine is added to aqueous sodium bromide.

(ii)     Outline, with the help of a chemical equation, why this reaction occurs.

The colour change in the reaction between aqueous chlorine and aqueous sodium iodide is very similar, but it differs with an excess of aqueous chlorine. Describe the appearance of the reaction mixture when excess aqueous chlorine has been added to aqueous sodium iodide.

Chloric(I) acid is a weak acid, but hydrochloric acid is a strong acid. Outline how this is indicated in the equation above.

State a balanced equation for the reaction of chloric(I) acid with water.

Outline, in terms of the equilibrium above, why it is dangerous to use an acidic toilet cleaner in combination with this kind of bleach.

Suggest why a covalent molecule, such as chloric(I) acid, is readily soluble in water.

Draw the Lewis (electron dot) structure of chloric(I) acid.

Predict the H–O–Cl bond angle in this molecule and explain this in terms of the valence shell electron pair repulsion (VSEPR) theory.

(i)     Deduce the coefficients required to balance the half-equations given below.

___ \({\text{Cl}}{{\text{O}}^ - } + \) ___ \({{\text{H}}^ + } + \) ___ \({{\text{e}}^ - } \rightleftharpoons \) ___ \({{\text{H}}_2}{\text{O}} + \) ___ \({\text{C}}{{\text{l}}^ - }\)

___ \({\text{SO}}_4^{2 - }\) ___ \({{\text{H}}^ + } + \) ___ \({{\text{e}}^ - } \rightleftharpoons \) ___ \({\text{S}}{{\text{O}}_2} + \) ___ \({{\text{H}}_2}{\text{O}}\)

(ii)     State the initial and final oxidation numbers of both chlorine and sulfur in the equations in part (i).

(iii)     Use the half-equations to deduce the balanced equation for the reaction between the chlorate(I) ion and sulfur dioxide.

State the formula of both ions present and the nature of the force between these ions.

Ions:

Nature of force:

State which atoms are covalently bonded.

Outline the source of these oxides.

State one product formed from their reaction with water.

State one environmental problem caused by these atmospheric pollutants.

Calculate the mass of the acid and determine its absolute and percentage uncertainty.

This known mass of acid, HA, was then dissolved in distilled water to form a \({\text{100.0 c}}{{\text{m}}^{\text{3}}}\) solution in a volumetric flask. A \({\text{25.0 c}}{{\text{m}}^{\text{3}}}\) sample of this solution reacted with \({\text{12.1 c}}{{\text{m}}^{\text{3}}}\) of a \({\text{0.100 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) NaOH solution. Calculate the molar mass of the acid.

The percentage composition of HA is 70.56% carbon, 23.50% oxygen and 5.94% hydrogen. Determine its empirical formula.

A solution of HA is a weak acid. Distinguish between a weak acid and a strong acid.

Describe an experiment, other than measuring the pH, to distinguish HA from a strong acid of the same concentration and describe what would be observed.

Outline two characteristics of a reversible reaction in a state of dynamic equilibrium.

Deduce the equilibrium constant expression, \({K_{\text{c}}}\), for the reaction.

Predict, with a reason, how each of the following changes affects the position of equilibrium.

The volume of the container is increased.

Ammonia is removed from the equilibrium mixture.

Define the term activation energy, \({E_{\text{a}}}\).

Ammonia is manufactured by the Haber process in which iron is used as a catalyst. Explain the effect of a catalyst on the rate of reaction.

Sketch the Maxwell–Boltzmann energy distribution curve for a reaction, labelling both axes and showing the activation energy with and without a catalyst.

Typical conditions used in the Haber process are 500 °C and 200 atm, resulting in approximately 15% yield of ammonia.

(i)     Explain why a temperature lower than 500 °C is not used.

(ii)     Outline why a pressure higher than 200 atm is not often used.

Define the term base according to the Lewis theory.

Define the term weak base according to the Brønsted-Lowry theory.

Deduce the formulas of conjugate acid-base pairs in the reaction below.

\[{\text{C}}{{\text{H}}_{\text{3}}}{\text{N}}{{\text{H}}_{\text{2}}}{\text{(aq)}} + {{\text{H}}_{\text{2}}}{\text{O(l)}} \rightleftharpoons {\text{C}}{{\text{H}}_{\text{3}}}{\text{NH}}_{\text{3}}^ + {\text{(aq)}} + {\text{O}}{{\text{H}}^ - }{\text{(aq)}}\]

Outline an experiment and its results which could be used to distinguish between a strong base and a weak base.

Define the term electronegativity.

Explain why the atomic radius of elements decreases across the period.

State the equations for the reactions of sodium oxide with water and phosphorus(V) oxide with water.

Suggest the pH of the solutions formed in part (c) (i).

Describe three tests that can be carried out in the laboratory, and the expected results, to distinguish between \({\text{0.10 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}{\text{ HCl(aq)}}\) and \({\text{0.10 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}{\text{ C}}{{\text{H}}_{\text{3}}}{\text{COOH(aq)}}\).

Explain whether BF₃ can act as a Brønsted-Lowry acid, a Lewis acid or both.

Describe the bonding and structure of sodium chloride.

State the formula of the compounds formed between the elements below.

Sodium and sulfur:

Magnesium and phosphorus:

Covalent bonds form when phosphorus reacts with chlorine to form \({\text{PC}}{{\text{l}}_{\text{3}}}\). Deduce the Lewis (electron dot) structure, the shape and bond angle in \({\text{PC}}{{\text{l}}_{\text{3}}}\) and explain why the molecule is polar.

Lewis (electron dot) structure:

Name of shape:

Bond angle:

Explanation of polarity of molecule:

The teacher made up \({\text{2.50 d}}{{\text{m}}^{\text{3}}}\) of the sodium thiosulfate solution using sodium thiosulfate pentahydrate crystals, \({\text{N}}{{\text{a}}_2}{{\text{S}}_{\text{2}}}{{\text{O}}_{\text{3}}} \bullet {\text{5}}{{\text{H}}_{\text{2}}}{\text{O}}\). Calculate the required mass of these crystals.

(i)     State the volumes of the liquids that should be mixed.

(ii)     State why it is important that the students use a similar beaker for both reactions.

(iii)     Explain, in terms of the collision theory, how decreasing the concentration of sodium thiosulfate would affect the time taken for the mark to be obscured.

(i)     Sketch and label, indicating an approximate activation energy, the Maxwell–Boltzmann energy distribution curves for two temperatures, \({T_1}\) and \({T_2}{\text{ }}({T_2} > {T_1})\), at which the rate of reaction would be significantly different.

(ii)     Explain why increasing the temperature of the reaction mixture would significantly increase the rate of the reaction.

(i)     One group suggested recording how long it takes for the pH of the solution to change by one unit. Calculate the initial pH of the original reaction mixture.

(ii)     Deduce the percentage of hydrochloric acid that would have to be used up for the pH to change by one unit.

(i)     Calculate the volume of sulfur dioxide, in \({\text{c}}{{\text{m}}^{\text{3}}}\), that the original reaction mixture would produce if it were collected at \(1.00 \times {10^5}{\text{ Pa}}\) and 300 K.

(ii)     Suggest why it is better to use a gas syringe rather than collecting the gas in a measuring cylinder over water.

Outline how electrical conductivity can be used to distinguish between a \({\text{0.200 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) solution of ethanoic acid, \({\text{C}}{{\text{H}}_{\text{3}}}{\text{COOH}}\), and a \({\text{0.200 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) solution of hydrochloric acid, HCl.

(i)     State an equation for the reaction of ethanoic acid with a solution of sodium hydrogencarbonate.

(ii)     Determine which is the limiting reagent. Show your working.

(iii)     Calculate the mass, in g, of carbon dioxide produced.

(i)     Determine the amount, in mol, of X in the gas syringe.

(ii)     Calculate the molar mass of X.

(i)     Identify the reagent necessary for this reaction to occur.

(ii)     Deduce the mechanism for the reaction using equations and curly arrows to represent the movement of electron pairs.

Determine the enthalpy change, in kJ mol\(^{ - 1}\), for this reaction, using Table 10 of the Data Booklet.

Bromoethene, \({\text{C}}{{\text{H}}_{\text{2}}}{\text{CHBr}}\), can undergo polymerization. Draw a section of this polymer that contains six carbon atoms.

Draw the Lewis structure of ammonia and state the shape of the molecule and its bond angles.

The conjugate acid of ammonia is the ammonium ion, \({\text{NH}}_4^ + \). Draw the Lewis structure of the ammonium ion and deduce its shape and bond angles.

Describe two different properties that could be used to distinguish between a \({\text{1.00 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) solution of a strong monoprotic acid and a \({\text{1.00 mol}}\,{\text{d}}{{\text{m}}^{ - 3}}\) solution of a weak monoprotic acid.

Explain, using the Brønsted-Lowry theory, how water can act either as an acid or a base. In each case identify the conjugate acid or base formed.

Draw a labelled diagram of a voltaic cell made from an \({\text{Fe(s)}}/{\text{F}}{{\text{e}}^{2 + }}{\text{(aq)}}\) half-cell connected to a \({\text{Cu(s)}}/{\text{C}}{{\text{u}}^{2 + }}{\text{(aq)}}\) half-cell. In your diagram identify the positive electrode (cathode), the negative electrode (anode) and the direction of electron flow in the external circuit.

Deduce the half-equations for the reactions taking place at the positive electrode (cathode) and negative electrode (anode) of this voltaic cell.

Deduce the overall equation for the reaction taking place in the voltaic cell and determine which species acts as the oxidizing agent and which species has been reduced.

Predict, giving a reason, a difference between the reactions of the same concentrations of hydrochloric acid and ethanoic acid with samples of calcium carbonate.

Dissolved carbon dioxide causes unpolluted rain to have a pH of approximately 5, but other dissolved gases can result in a much lower pH. State one environmental effect of acid rain.

(i) 200.0 g of air was heated by the energy from the complete combustion of 1.00 mol phosphine. Calculate the temperature rise using section 1 of the data  booklet and the data below.

Standard enthalpy of combustion of phosphine,
Specific heat capacity of air = 1.00Jg⁻¹K⁻¹ = 1.00 kJkg⁻¹K⁻¹

(ii) The oxide formed in the reaction with air contains 43.6 % phosphorus by mass. Determine the empirical formula of the oxide, showing your method.

(iii) The molar mass of the oxide is approximately 285gmol⁻¹. Determine the molecular formula of the oxide.

(i) State the equation for the reaction of this oxide of phosphorus with water.

(ii) Predict how dissolving an oxide of phosphorus would affect the pH and electrical conductivity of water.

pH:

Electrical conductivity:

(iii) Suggest why oxides of phosphorus are not major contributors to acid deposition.

(iv) The levels of sulfur dioxide, a major contributor to acid deposition, can be minimized by either pre-combustion and post-combustion methods. Outline one technique of each method.

Pre-combustion:

Post-combustion:

Sketch a Maxwell–Boltzmann distribution curve for a chemical reaction showing the activation energies with and without a catalyst.

Sketch a curve on the graph to show the volume of gas produced over time if the same mass of crushed calcium carbonate is used instead of lumps. All other conditions remain constant.

State and explain the effect on the rate of reaction if ethanoic acid of the same concentration is used in place of hydrochloric acid.

Outline why pH is more widely used than [H⁺] for measuring relative acidity.

Outline why H₃PO₄/HPO₄²⁻ is not a conjugate acid-base pair.

Describe the bonding in metals.

Titanium exists as several isotopes. The mass spectrum of a sample of titanium gave the following data:

Calculate the relative atomic mass of titanium to two decimal places.

State the number of protons, neutrons and electrons in the \({}_{22}^{48}{\text{Ti}}\) atom.

State the full electron configuration of the \({}_{22}^{48}{\text{Ti}}\)²⁺ ion.

Explain why an aluminium-titanium alloy is harder than pure aluminium.

State the type of bonding in potassium chloride which melts at 1043 K.

A chloride of titanium, TiCl₄, melts at 248 K. Suggest why the melting point is so much lower than that of KCl.

Formulate an equation for this reaction.

Suggest one disadvantage of using this smoke in an enclosed space.

Identify the amphiprotic species.

Identify one conjugate acid-base pair in the reaction.

Calculate the amount, in mol, of NaOH(aq) used.

Calculate the molar mass of the acid.

Calculate [H⁺] in the NaOH solution.

(i)     State the equilibrium constant expression for the dissociation of water.

(ii)     Explain why even a very acidic aqueous solution still has some \({\text{O}}{{\text{H}}^ - }\) ions present in it.

(iii)     State and explain the effect of increasing temperature on the equilibrium constant above given that the dissociation of water is an endothermic process.

(iv)     The pH of a solution is 2. If its pH is increased to 6, deduce how the hydrogen ion concentration changes.

In carbonated drinks containing dissolved carbon dioxide under high pressure, the

following dynamic equilibrium exists.

\[{\text{C}}{{\text{O}}_2}({\text{aq)}} \rightleftharpoons {\text{C}}{{\text{O}}_2}({\text{g)}}\]

Describe the effect of opening a carbonated drink container and outline how this

equilibrium is affected.

(i)     Explain the shape of the curve.

(ii)     Copy the above graph on your answer sheet and sketch the curve you would obtain if double the volume of hydrochloric acid solution of half the concentration as in the example above is used instead, with all other variables kept constant from the original. Explain why the shape of the curve is different.

(iii)     Outline one other way in which the rate of this reaction can be studied in a school laboratory. Sketch a graph to illustrate how the selected variable would change with time.

(iv)     Define the term activation energy and state one reason why the reaction between calcium carbonate and hydrochloric acid takes place at a reasonably fast rate at room temperature.

One example of a homologous series is the alcohols. Describe two features of a homologous series.

The IUPAC name of X is 4-methylpentan-1-ol. State the IUPAC names of Y and Z.

Y:

Z:

State the reagents and reaction conditions used to convert X to Y and X to Z.

X to Y:

X to Z:

Z is an example of a weak acid. State what is meant by the term weak acid.

Discuss the volatility of Y compared to Z.

Determine the percentage by mass of carbon and hydrogen in J, using the combustion data.

Determine the percentage by mass of chlorine in J, using the precipitation data.

The molar mass was determined to be \({\text{131.38 g}}\,{\text{mo}}{{\text{l}}^{ - 1}}\). Deduce the molecular formula of J.

After heating 3.760 g of a silver oxide 3.275 g of silver remained. Determine the empirical formula of Ag_xO_y.

Suggest why the final mass of solid obtained by heating 3.760 g of Ag_xO_y may be greater than 3.275 g giving one design improvement for your proposed suggestion. Ignore any possible errors in the weighing procedure.

Naturally occurring silver is composed of two stable isotopes, ¹⁰⁷Ag and ¹⁰⁹Ag.

The relative atomic mass of silver is 107.87. Show that isotope ¹⁰⁷Ag is more abundant.

Some oxides of period 3, such as Na₂O and P₄O₁₀, react with water. A spatula measure of each oxide was added to a separate 100 cm³ flask containing distilled water and a few drops of bromothymol blue indicator.

The indicator is listed in section 22 of the data booklet.

Deduce the colour of the resulting solution and the chemical formula of the product formed after reaction with water for each oxide.

Explain the electrical conductivity of molten Na₂O and P₄O₁₀.

Outline the model of electron configuration deduced from the hydrogen line emission spectrum (Bohr’s model).

Estimate the H−N−H bond angle in methanamine using VSEPR theory.

Ammonia reacts reversibly with water.

NH₃(g) + H₂O(l) \( \rightleftharpoons \) NH₄⁺(aq) + OH⁻(aq)

Explain the effect of adding H⁺(aq) ions on the position of the equilibrium.

Hydrazine reacts with water in a similar way to ammonia. Deduce an equation for the reaction of hydrazine with water.

Outline, using an ionic equation, what is observed when magnesium powder is added to a solution of ammonium chloride.

Hydrazine has been used as a rocket fuel. The propulsion reaction occurs in several stages but the overall reaction is:

N₂H₄(l) → N₂(g) + 2H₂(g)

Suggest why this fuel is suitable for use at high altitudes.

Determine the enthalpy change of reaction, ΔH, in kJ, when 1.00 mol of gaseous hydrazine decomposes to its elements. Use bond enthalpy values in section 11 of the data booklet.

N₂H₄(g) → N₂(g) + 2H₂(g)

The standard enthalpy of formation of N₂H₄(l) is +50.6 kJ\(\,\)mol⁻¹. Calculate the enthalpy of vaporization, ΔH_vap, of hydrazine in kJ\(\,\)mol⁻¹.

N₂H₄(l) → N₂H₄(g)

(If you did not get an answer to (f), use −85 kJ but this is not the correct answer.)

Calculate, showing your working, the mass of hydrazine needed to remove all the dissolved oxygen from 1000 dm³ of the sample.

Calculate the volume, in dm³, of nitrogen formed under SATP conditions. (The volume of 1 mol of gas = 24.8 dm³ at SATP.)

Outline why the rate of the reaction decreases with time.

Sketch, on the same graph, the expected results if the experiment were repeated using powdered magnesium, keeping its mass and all other variables unchanged.

Nitrogen dioxide and carbon monoxide react according to the following equation:

NO₂(g) + CO(g) \( \rightleftharpoons \) NO(g) + CO₂(g)               ΔH = –226 kJ

Calculate the activation energy for the reverse reaction.

State the equation for the reaction of NO₂ in the atmosphere to produce acid deposition.

The following reaction was allowed to reach equilibrium at 761 K.

H₂ (g) + I₂ (g) \( \rightleftharpoons \) 2HI (g)               ΔH^θ < 0

Outline the effect, if any, of each of the following changes on the position of equilibrium, giving a reason in each case.

Identify two different amphiprotic species in the above reactions.

State what is meant by the term conjugate base.

State the conjugate base of the hydroxide ion, OH^–.

A student working in the laboratory classified HNO₃, H₂SO₄, H₃PO₄ and HClO₄ as acids based on their pH. He hypothesized that “all acids contain oxygen and hydrogen”.

Evaluate his hypothesis.

Identify the formula and state symbol of X.

Suggest why the experiment should be carried out in a fume hood or in a well-ventilated laboratory.

The precipitate of sulfur makes the mixture cloudy, so a mark underneath the reaction mixture becomes invisible with time.

10.0 cm³ of 2.00 mol dm^-3 hydrochloric acid was added to a 50.0 cm³ solution of sodium thiosulfate at temperature, T1. Students measured the time taken for the mark to be no longer visible to the naked eye. The experiment was repeated at different concentrations of sodium thiosulfate.

Show that the hydrochloric acid added to the flask in experiment 1 is in excess.

Draw the best fit line of \(\frac{1}{{\rm{t}}}\) against concentration of sodium thiosulfate on the axes provided.

A student decided to carry out another experiment using 0.075 mol dm^-3 solution of sodium thiosulfate under the same conditions. Determine the time taken for the mark to be no longer visible.

An additional experiment was carried out at a higher temperature, T₂.

(i) On the same axes, sketch Maxwell–Boltzmann energy distribution curves at the two temperatures T₁ and T₂, where T₂ > T₁.

(ii) Explain why a higher temperature causes the rate of reaction to increase.

Suggest one reason why the values of rates of reactions obtained at higher temperatures may be less accurate.