Group 16 Flashcards

1
Q

Describe variation in metallic character down the group and across the periods in p-block

A
  1. Increasing non-metallic behaviour across the period

2. Increase non-metal to metalloid to metal down a group

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2
Q

What is the maximum oxidation state in group 16

A
  1. +6

2. Doesn’t exist for O

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3
Q

What oxidation states are available for oxygen

A
  1. -2, -1, 0
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4
Q

What are the two common allotropes of oxygen

A
  1. O2 and O3
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5
Q

Describe O2

A
  1. Paramagnetic- unpaired electrons in its electronic ground state
  2. Forms a pale blue liquid and solid at low temperatures
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6
Q

Describe how O2 is synthesised industrially

A
  1. Fractional distillation of liquid air
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7
Q

Describe how O2 is synthesised in the lab

A
  1. Electrolysis of water or decomposition of either potassium chlorate or hydrogen peroxide
  2. KClO3 –> 2KCl + 3O2
  3. 2H2O2 –> 2H2O + O2
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8
Q

Describe bonding in ozone

A
  1. Pale blue gas at room temp
  2. Bond length in between single bond of hydrogen peroxide and double bond of O2
  3. The pi-bonding is involving a p-orbital on O with 2e- in it and 1e in p-orbital on each end O
  4. 2e in bonding MO which is stretched across 2 bonds so pi bond order is 0.5
  5. Overall bond order (single + pi-bond) = 1.5
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9
Q

What are physical properties of oxygen

A
  1. Strong oxidising agent

3. O3 is stronger than O2

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10
Q

Why is S-S stronger than O-O

A
  1. Lone pairs of e- that repel each other and weakens O-O single bond
  2. O is smaller than S so have stronger repulsions and therefore weaker bonds
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11
Q

Describe general trend in bond strength down the group

A
  1. Atom size increases as we go down a group, so atom-atom contact increases
  2. 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
  3. As we go down groups bond energy decreases
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12
Q

Why does S have more allotropic forms than any other element

A
  1. Large number of rings that can be formed with S-S bonds and the many ways it can pack in the solid state
  2. Preference for formation of single bonds as stronger than multiple
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13
Q

What happens when S8 is heated

A
  1. Heat to 119 degrees- melts –> yellow liquid, becomes less viscous
  2. Continue to 159 degrees –> Viscosity increases dramatically, now s8 rings open to form S8 chains, these interact to form S16, S24 etc
  3. Heat further- viscosity decreases again, cleave apart long chains to form smaller units
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14
Q

Why is there difference in behaviour between O and S

A
  1. Bond strengths
  2. O pi-bond is more than twice the strength of the single bond
  3. Formation of O=O is favoured compared to 2*O-O and the opposite is true for S
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15
Q

What happens to the energy difference between s and p orbitals as you go down the group

A
  1. Increases

2. Less s-p mixing and bonds become more p-like character

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16
Q

As you go down the group what happens to the hydrides

A
  1. The H-M-H angles get closer to 90 degrees

2. Les sp2 type more p orbital

17
Q

What happens to the boiling point of group 16 hydrides down the group

A
  1. Decrease from O - hydrogen bond

2. Then increase - Van der Waals increasingly polarisable as we go down the group

18
Q

Describe acidity from group 15-17

A
  1. NH3 is most basic
  2. Acidity increases from left to right along with increasing electronegativity
  3. Acidity also increases down the groups as bonds get weaker so reduce stability and increase acidity
19
Q

Describe water

A
  1. Solid has lower density than liquid due to opening up of H-bonding
  2. Ice floats on water
  3. At least 9 distinct forms
20
Q

Describe H2O2

A
  1. v pale blue liquid
  2. Liquid at rt, more dense and viscous than H2O
  3. OS= -1
  4. Can be both a strong oxidising and reducing agent
21
Q

Show disproportionation of H2O2

A
  1. H2O2 –> H2O + 1/2 O2
  2. Metal and glass catalysed
  3. Stored in plastic containers
22
Q

What is the only halide of oxygen

A
  1. Fluoride
23
Q

Describe different oxygen halides

A
  1. OF2- colourless gas, v toxic, radical decomp to F2 and O2
  2. OFH- colourless liquid, v toxic, decomp to HF and O2 at RT
  3. O2F2- prepared by passing electrical discharge through F2 and O2, solid which decomposes at RT over days
24
Q

Describe bonding in O2F2

A
  1. Bonding of fluorine to the O2 molecule is by overlap of the 2p on fluorine with pi* on O2
  2. 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.
25
Q

Describe how SF6 can be formed

A
  1. F is oxidising enough to allow S to get to OS of 6- thermodynamically unstable but kinetically stable
  2. The stability is a result of 6 F atoms surrounding the S and stopping attack at delta+ centre
  3. Favourable as F-F bond in unfavourable so negative enthalpy of formation
  4. Cl-Cl bond is favourable so SCl6 is less stable
26
Q

Describe SF4

A
  1. 10 Valence electrons but an still use as lewis acid
  2. Readily hydrolysed
  3. Properties as both lewis acid and base
  4. See-saw structure
27
Q

Describe S2F2

A
  1. Analogue of O2F2

2. Two isomers

28
Q

Describe sulfur oxides

A
  1. S=O bonding even though multiple bonding is a feature of the top row elements
  2. sigma and pi bond components are comparable in sulfur oxide bonds so s=o can be made
29
Q

What are important oxides of sulfur

A
  1. SO2- gas- Cyclic trimer based on S3O3 ring in solid state

2. SO3

30
Q

Describe SeO2

A
  1. Chain in solid state

2. SeO2 molecules in gas phase