Group 16 Flashcards
Describe variation in metallic character down the group and across the periods in p-block
- Increasing non-metallic behaviour across the period
2. Increase non-metal to metalloid to metal down a group
What is the maximum oxidation state in group 16
- +6
2. Doesn’t exist for O
What oxidation states are available for oxygen
- -2, -1, 0
What are the two common allotropes of oxygen
- O2 and O3
Describe O2
- Paramagnetic- unpaired electrons in its electronic ground state
- Forms a pale blue liquid and solid at low temperatures
Describe how O2 is synthesised industrially
- Fractional distillation of liquid air
Describe how O2 is synthesised in the lab
- Electrolysis of water or decomposition of either potassium chlorate or hydrogen peroxide
- KClO3 –> 2KCl + 3O2
- 2H2O2 –> 2H2O + O2
Describe bonding in ozone
- Pale blue gas at room temp
- Bond length in between single bond of hydrogen peroxide and double bond of O2
- The pi-bonding is involving a p-orbital on O with 2e- in it and 1e in p-orbital on each end O
- 2e in bonding MO which is stretched across 2 bonds so pi bond order is 0.5
- Overall bond order (single + pi-bond) = 1.5
What are physical properties of oxygen
- Strong oxidising agent
3. O3 is stronger than O2
Why is S-S stronger than O-O
- Lone pairs of e- that repel each other and weakens O-O single bond
- O is smaller than S so have stronger repulsions and therefore weaker bonds
Describe general trend in bond strength down the group
- Atom size increases as we go down a group, so atom-atom contact increases
- As atom size increases so does the size of the orbitals and as atoms increase in size the distance between them increases and bond strength decreases
- As we go down groups bond energy decreases
Why does S have more allotropic forms than any other element
- Large number of rings that can be formed with S-S bonds and the many ways it can pack in the solid state
- Preference for formation of single bonds as stronger than multiple
What happens when S8 is heated
- Heat to 119 degrees- melts –> yellow liquid, becomes less viscous
- Continue to 159 degrees –> Viscosity increases dramatically, now s8 rings open to form S8 chains, these interact to form S16, S24 etc
- Heat further- viscosity decreases again, cleave apart long chains to form smaller units
Why is there difference in behaviour between O and S
- Bond strengths
- O pi-bond is more than twice the strength of the single bond
- Formation of O=O is favoured compared to 2*O-O and the opposite is true for S
What happens to the energy difference between s and p orbitals as you go down the group
- Increases
2. Less s-p mixing and bonds become more p-like character
As you go down the group what happens to the hydrides
- The H-M-H angles get closer to 90 degrees
2. Les sp2 type more p orbital
What happens to the boiling point of group 16 hydrides down the group
- Decrease from O - hydrogen bond
2. Then increase - Van der Waals increasingly polarisable as we go down the group
Describe acidity from group 15-17
- NH3 is most basic
- Acidity increases from left to right along with increasing electronegativity
- Acidity also increases down the groups as bonds get weaker so reduce stability and increase acidity
Describe water
- Solid has lower density than liquid due to opening up of H-bonding
- Ice floats on water
- At least 9 distinct forms
Describe H2O2
- v pale blue liquid
- Liquid at rt, more dense and viscous than H2O
- OS= -1
- Can be both a strong oxidising and reducing agent
Show disproportionation of H2O2
- H2O2 –> H2O + 1/2 O2
- Metal and glass catalysed
- Stored in plastic containers
What is the only halide of oxygen
- Fluoride
Describe different oxygen halides
- OF2- colourless gas, v toxic, radical decomp to F2 and O2
- OFH- colourless liquid, v toxic, decomp to HF and O2 at RT
- O2F2- prepared by passing electrical discharge through F2 and O2, solid which decomposes at RT over days
Describe bonding in O2F2
- Bonding of fluorine to the O2 molecule is by overlap of the 2p on fluorine with pi* on O2
- Fluorine is unique in being more electronegative than oxygen, so there is little increase in pi* electron density thus preserving the double bond of O2.
Describe how SF6 can be formed
- F is oxidising enough to allow S to get to OS of 6- thermodynamically unstable but kinetically stable
- The stability is a result of 6 F atoms surrounding the S and stopping attack at delta+ centre
- Favourable as F-F bond in unfavourable so negative enthalpy of formation
- Cl-Cl bond is favourable so SCl6 is less stable
Describe SF4
- 10 Valence electrons but an still use as lewis acid
- Readily hydrolysed
- Properties as both lewis acid and base
- See-saw structure
Describe S2F2
- Analogue of O2F2
2. Two isomers
Describe sulfur oxides
- S=O bonding even though multiple bonding is a feature of the top row elements
- sigma and pi bond components are comparable in sulfur oxide bonds so s=o can be made
What are important oxides of sulfur
- SO2- gas- Cyclic trimer based on S3O3 ring in solid state
2. SO3
Describe SeO2
- Chain in solid state
2. SeO2 molecules in gas phase