Question 21M.2.hl.TZ2.2
Date | May 2021 | Marks available | [Maximum mark: 18] | Reference code | 21M.2.hl.TZ2.2 |
Level | hl | Paper | 2 | Time zone | TZ2 |
Command term | Deduce, Describe, Estimate, Explain, Justify, State, Suggest | Question number | 2 | Adapted from | N/A |
The properties of elements can be predicted from their position in the periodic table.
Explain why Si has a smaller atomic radius than Al.
[2]
nuclear charge/number of protons/Z/Zeff increases «causing a stronger pull on the outer electrons» ✓
same number of shells/«outer» energy level/shielding ✓

Explain why the first ionization energy of sulfur is lower than that of phosphorus.
[2]
P has «three» unpaired electrons in 3p sub-level AND S has one full 3p orbital «and two 3p orbitals with unpaired electrons»
OR
P: [Ne]3s23px13py13pz1 AND S: [Ne]3s23px23py13pz1 ✓
Accept orbital diagrams for 3p sub-level for M1. Ignore other orbitals or sub-levels.
repulsion between paired electrons in sulfur «and therefore easier to remove» ✓
Accept “removing electron from S gives more stable half-filled sub-level" for M2.

State the condensed electron configurations for Cr and Cr3+.
[2]
Cr:
[Ar] 4s13d5 ✓
Cr3+:
[Ar] 3d3 ✓
Accept “[Ar] 3d54s1”.
Accept “[Ar] 3d34s0”.
Award [1 max] for two correct full electron configurations “1s22s22p63s23p64s13d5 AND 1s22s22p63s23p63d3”.
Award [1 max] for 4s13d5 AND 3d3.
Describe metallic bonding and how it contributes to electrical conductivity.
[3]
electrostatic attraction ✓
between «a lattice of» cations/positive «metal» ions AND «a sea of» delocalized electrons ✓
mobile electrons responsible for conductivity
OR
electrons move when a voltage/potential difference/electric field is applied ✓
Do not accept “nuclei” for “cations/positive ions” in M2.
Accept “mobile/free” for “delocalized” electrons in M2.
Accept “electrons move when connected to a cell/battery/power supply” OR “electrons move when connected in a circuit” for M3.


Deduce, giving a reason, which complex ion [Cr(CN)6]3− or [Cr(OH)6]3− absorbs higher energy light. Use section 15 of the data booklet.
[1]
[Cr(CN)6]3− AND CN−/ligand causes larger splitting «in d-orbitals compared to OH−»
OR
[Cr(CN)6]3− AND CN−/ligand associated with a higher Δ/«crystal field» splitting energy/energy difference «in the spectrochemical series compared to OH− » ✓
Accept “[Cr(CN)6]3− AND «CN−» strong field ligand”.

[Cr(OH)6]3− forms a green solution. Estimate a wavelength of light absorbed by this complex, using section 17 of the data booklet.
[1]
any value or range between 647 and 700 nm ✓

Deduce the Lewis (electron dot) structure and molecular geometry of sulfur tetrafluoride, SF4, and sulfur dichloride, SCl2.
[4]
SF4/SCl2 structure does not have to be 3-D for mark.
Penalize missing lone pairs of electrons on halogens once only.
Accept any combination of dots, lines or crosses for bonds/lone pairs.
Accept “non-linear” for SCl2 molecular geometry.
Award [1] for two correct electron domain geometries, e.g. trigonal bipyramidal for SF4 and tetrahedral for SCl2.
Suggest, giving reasons, the relative volatilities of SCl2 and H2O.
[3]
H2O forms hydrogen bonding «while SCl2 does not» ✓
SCl2 «much» stronger London/dispersion/«instantaneous» induced dipole-induced dipole forces ✓
Alternative 1:
H2O less volatile AND hydrogen bonding stronger «than dipole–dipole and dispersion forces» ✓
Alternative 2:
SCl2 less volatile AND effect of dispersion forces «could be» greater than hydrogen bonding ✓
Ignore reference to Van der Waals.
Accept “SCl2 has «much» larger molar mass/electron density” for M2.

