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Last updated 1:09 PM on 4/16/26
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24 Terms

1
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requirements for 2 solutions to mix

- the energy required to break the intramolecular forces must be similar or less than the energy required to form intermolecular forces between the 2 solutions

- eg water and hexane do not mix well as water has strong hydrogen bonding but hexane only has weak LDF

- so only new LDFs can form between them which is not energetically favorable

2
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explain why 2-methylpentane can dissolve in hexane but not water. (3)

- 2-methylpentane cannot form hydrogen bonds with water so insoluble

- soluble in hexane as LDF in both compounds are similar in strength and magnitude hence they mix well

3
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explain why potassium bromide can dissolve in water but not in hexane. (3)

- KBr is ionic so when dissolved in water, the ions (K+ and Br-) become hydrated

- this is when the oxygen end of water is attracted to K+, while the hydrogen end of water is attracted to Br-

- the energy released from this hydration causes the ionic lattice to break apart

- doesn't dissolve in hexane since LDF forces are much weaker than the ionic forces holding KBr together

4
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the common oxidation numbers of chromium are +2, +3, +6.

give a reason, in terms of ionisation energies, why chromium can show variable oxidation numbers. (1)

Cr configuration is [Ar] 3d5 4s1

gradual increase in successive ionisation energy due to similar shielding in 3d5 and 4s1 orbital

<p>Cr configuration is [Ar] 3d5 4s1</p><p>gradual increase in successive ionisation energy due to similar shielding in 3d5 and 4s1 orbital</p>
5
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2Mg(NO₃)₂ → 2MgO + 4NO₂ + O₂

explain, in terms of all relevant oxidation number, why this is redox. (3)

to find the oxidation number of 2Mg(NO₃)₂:

consider Mg = +2 and NO₃⁻: as O is -6, N must = +5

N is reduced from +5 to +4

O is oxidised from -2 to 0

6
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explain why [Zn(H₂O)₆]²⁺ is colourless. (2)

- zinc has a full 3d subshell

- so d-d transitions cannot take place

7
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the data show the enthalpy changes of reaction when 1 mol of different acids is neutralised by NaOH solution.

comment on the relative enthalpy changes of reaction, using the data below and include any relevant equations. (6)

HCl: -58 kJ mol-1

HNO₃: -58 kJ mol-1

H₂SO₄: -115 kJ mol-1

CH₃COOH: -56 kJ mol-1

HCl and HNO₃

- same value as they are strong acids that completely dissociate into ions in solution

- H⁺ + OH⁻ → H₂O

H₂SO₄

- H₂SO₄ is diprotic so 1 mol provides 2H⁺

- hence value is 2x that of HCl / HNO₃

CH₃COOH

- weak acid so only partially dissociates into ions

- CH₃COOH ⇌ CH₃COO⁻ + H⁺

- some energy is needed to break OH bonds (endothermic) to release H⁺ so enthalpy change of neutralisation is less than strong acids

8
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glycolic acid (HOCH₂COOH) has an acid dissociation constant of 1.5x10⁻⁴ compared with a value of 1.7x10⁻⁵ mol dm-3 for ethanoic acid (CH₃COOH).

give a possible explanation as to why the value of Ka for glycolic acid is 10x larger than that of ethanoic acid. (2)

- the hydroxyl group -OH in glycolic acid is electron withdrawing, which means it pulls the e- density away from the rest of the molecule

- while the methyl group -CH₃ in ethanoic acid is electron donating, which means it pushes e- towards the rest of the molecule

- for an acid to be strong, its anion (eg CH₃COO⁻, HOCH₂COO⁻) must be stable

- an electron withdrawing group is able to spread out the negative charge of the COO⁻, making it more stable so its comfortable existing as a negative ion

- a stable anion has a weaker O-H bond so H⁺ can be lost more easily

9
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2MnO₄⁻ + 5C₂O₄²⁻ + 16H⁺ → 2Mn²⁺ + 10CO₂ + 8H₂O

the reaction starts slowly, then rate of reaction increases, before it decreases again. explain this sequence. (3)

- initial rate is slow because both reacting species are negatively charged

- rate of reaction increase due to formation of Mn²⁺ ions which act as an autocatalyst

- the rate decreases as reactants are used up

10
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give a reason why a solid is not included in the expression for Kc. (1)

because the concentration of a solid is constant

11
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LiCl theoretical lattice energy: -845

LiCl experimental lattice energy: -848

MgI₂ theoretical lattice energy: -1944

MgI₂ experimental lattice energy: -2327

comment on the theoretical and experimental lattice energy values, giving the reasons for any differences and similarities. (6)

- LiCl is almost 100% ionic

- while difference in theoretical and experimental value suggest that MgI₂ has some covalent character

- since Mg²⁺ has a higher charge density than Li⁺ so it has a larger polarising power

- while I⁻ is larger than Cl⁻ so it is more easily polarised

12
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give a reason why the catalysis of Fe²⁺ is possible. (1)

due to variable oxidation number in TM

13
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predict, with reason, whether water is acidic, alkaline or neutral.

neutral since [OH⁻] = [H⁺]

14
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predict, with reason, the sign of the enthalpy change for the ionisation of water. (1)

- positive (endothermic)

- as bond breaking requires energy

<p>- positive (endothermic)</p><p>- as bond breaking requires energy</p>
15
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compare and contrast the origin of colour of a copper(II) complex with the origin of colour of a copper(II) ion flame test. (6)

- difference in energy levels determines colour of complex ion and colour in flame test

- in a flame test, the heat energy cause electrons to become promoted to an excited state

- the return of excited electron to lower energy state result in colour

- in a complex ion, d orbitals are split in energy by ligands

- d-d transitions cause different frequency of visible light to be absorbed

- light that is not absorbed is transmitted to give colour

16
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rank the lattice energies of the hydrides NaH, KH and MgH₂

MgH₂ > NaH > KH

lattice energy of MgH₂ should be 2x more than that of NaH and KH because higher charge of Mg²⁺ and 2H⁻

NaH is more exothermic than KH because Na⁺ is smaller than K⁺, leading to stronger electrostatic attraction with H

17
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one of the systems controlling the pH of blood is the carbonic-acid hydrogencarbonate buffer system.

H₂CO₃ ⇌ H⁺ + HCO₃⁻

explain how this buffer system helps to control the pH of blood when extra CO2 is present due to strenuous exercise. (3)

- carbon dioxide dissolved in the blood forms carbonic acid (H₂CO₃)

- which causes the equilibrium to shift the the RHS so more H⁺ is formed

- reservoir of HCO₃⁻ combine with H⁺ to control blood pH

18
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[Cr(H₂O)₆]³⁺ + EDTA⁴⁻ ⇌ [CrEDTA]⁻ + 6H₂O

the Kc is 2.51 x 10²³

by considering the equilibrium for this reaction and changes in entropy, comment on the value of the equilibrium constant. (3)

- Kc is larger which suggest that the equilibrium lies to the right

- 2 mol of reactant form 7 mol of products

- this increases entropy of the system

19
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give 2 reasons why you would expect the ∆S(sys) to be positive. (2)

- more gas moles on the right

- gas and liquid is formed from solids

20
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a commercial nitric acid solution, HNO₃, has a concentration of 15.9 mol dm-3.

a 15cm3 sample was made up to 100cm3 by adding deionised waetr.

calculate the pH of this solution. (2)

initial vol: 15

final vol: 100

initial conc: 15.9

final conc: ?

so 15 x 15.9 = 100 x ?

so final conc = 2.385

21
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name 2 properties of ions that affect their enthalpy change of hydration

- ionic radius

- ionic charge

22
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HCl is addded to aqueous Na₂CO₃.

the reaction takes place in 2 steps because CO₃²⁻ is diprotic.

the equation taking place in the first step is Na₂CO₃ + HCl → NaHCO₃ + NaCl.

write the equation for the reaction taking place during the second equivalent point. (1)

HCO₃⁻ + H⁺ → CO₂ + H₂O

23
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Na₂CO₃ + HCl → NaHCO₃ + NaCl.

explain how the solution can act as a buffer. (3)

- large resevoir of acid and its conjugate base (CO₃²⁻ and HCO₃⁻

- so CO₃²⁻ can react with added H⁺ (CO₃²⁻ + H⁺ → HCO₃⁻)

- while HCO₃⁻ can react with added OH⁻ (HCO₃⁻ + OH⁻ → CO₃²⁻ + H₂O)

24
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define the term orbital (2)

- a region where theres a 95% chance of finding an electron

- contain a pair of e- with opposite spins