Module 3: The Periodic Table Flashcards

(183 cards)

1
Q

The periodic table
What were the only ways to categorise elements in the 1800s

A

By their physical and chemical properties or their relative atomic mass

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2
Q

The periodic table
In 1817 what did dobereiner attempt to do and what were they called

A

Group similar elements and the groups were called dobereiners triads

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3
Q

The periodic table
What groups did dobereiner create

A

Saw bromine chlorine and iodine had similar characteristic
Realises properties of bromine fell halfway between chlorine and iodine
Found groups of three eg lithium sodium and potassium

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4
Q

The periodic table
What did john newlands do

A

Tried to make a table of elements in 1863and noticed if her arranged elements in order of mass similar elements appeared regularly

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5
Q

The periodic table
What was the law of octaves

A

John newlands found every eighth elements was similar but this pattern broke down on third row

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6
Q

The periodic table
What did dmitri Mendeleev do

A

In 1869 produced a better table which wasn’t far off current table

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7
Q

The periodic table
How did Mendeleev arrange elements

A

By atomic mass and left gaps in the table where the next element didn’t seem to fit so could keep elements with similar chemical properties in same groups

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8
Q

The periodic table
What did Mendeleev predict

A

Properties of undiscovered elements

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9
Q

The periodic table
How is the modern periodic table arranged

A

By increasing proton number

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10
Q

The periodic table
How is the periodic table laid out

A

Into periods (rows) and groups (columns)

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11
Q

The periodic table
What do all elements in same period have and what does this mean

A

Same number of electron shells and means there are repeating trends in physical and chemical properties across periods

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12
Q

The periodic table
What are trends in properties called

A

Periodicity

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13
Q

The periodic table
What do all elements within one groups have and what does this mean

A

All have same number of electrons in outer shell and have similar chemical properties

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14
Q

Ionisation energies
What does it mean if and atom or molecule has been ionised

A

Electrons have been removed

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15
Q

Ionisation energies
Definition for the first ionisation energy

A

Energy needed to remove 1 mole of electrons from 1 mole of gaseous atoms

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16
Q

Ionisation energies
What type of process is it to ionise an atom or molecule and why

A

Have to put energy in so and endothermic process

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17
Q

Ionisation energies
Equation for first ionisation energies

A

X (g) —> X+ (g) + e-

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18
Q

Ionisation energies
Important to rember when writing ionisation energy equations

A

Must use gas symbol (g) because ionisation energies are measured for gaseous atoms

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19
Q

Ionisation energies
What does the lower ionisation energy mean

A

Easier to form an ion

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20
Q

Ionisation energies
What factors affect ionisation energies

A

Nuclear charge
Atomic radius
Shielding

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21
Q

Ionisation energies
How does nuclear charge affect ionisation energy

A

More protons in the nucleus, more positively charged the nucleus is and the stronger attraction for the electrons

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22
Q

Ionisation energies
How does atomic radius affect ionisation energy

A

Attraction decreases rapidly with distance, an electron close to the nucleus will be much more strongly attracted than one further away therefore require more energy to remove

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23
Q

Ionisation energies
How does shielding affect ionisation energy

A

As number of electrons increases, there’s more shells therefore shielding from inner shells and less attraction between nucleus and outer electron

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24
Q

Ionisation energies
What does a high ionisation energy mean

A

Strong attraction between the electron and the nucleus so more energy is ended to overcome the attraction and removed the electron

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25
Ionisation energies What happens to ionisation energies as you go down a group
Decreases
26
Ionisation energies What does ionisation energies decrease down a. Group
Elements have more electron shells compared to one above. Extra shells means that atomic radius is larger so outer electrons are further away from nucleus which means there a weaker attraction to the nucleus due to shielding from the inner shells
27
Ionisation energies What does ionisation energies decreasing down the group give evidence for
Electron shells existing
28
Ionisation energies What happens to the ionisation energy across a period
Increases
29
Ionisation energies Why does ionisation energy increase actions a period
Number of protons is increasing so positive charge in nucleus increases, electrons are pulled closer to the nucleus making the atomic radius smaller so stronger stronger attraction and more energy required to overcome it
30
Ionisation energies What are the two exceptions to ionisation energies increasing across a period
First ionisation energy decreases between groups 2 and 3 and between groups 5 and 6
31
Ionisation energies Why is there a drop in ionisation energy between groups 2 and 3 as an expection to period trend
Due to subshell structure
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Ionisation energies Why is there a drop in ionisation energy between groups 2 and 3 due to subshell structure
Outer electron in group 3 is in a p orbital rather than and s orbital A p orbital is slightly higher energy than an s orbital in same shell so electron on average is further from nucleus P orbital also has additional shielding These factors override effect of increasing nucleus charge
33
Ionisation energies Why is there a drop in ionisation energy between groups 5 and 6 as an exception to periodicity
Due to p orbital repulsion
34
Ionisation energies Why is there a drop in ionisation energies between group 5 and 6 due to p orbital repulsion
In group 5 elements the electron is being removed from a single occupied orbital In group 6 elements electron is removed from an orbital with 2 electrons The repulsion between the two electrons in an orbital means that they’re easier to remove
35
Ionisation energies What are successive ionisation energies
Each time you remove and electron after the first time and can remove all electrons to leave only the nucleus
36
Ionisation energies What is the equation for the second ionisation energy
X+ (g) —> X 2+ (g) + e-
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Ionisation energies What does a graph of successive ionisation energies provide evidence for
Shell structure of atoms
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Ionisation energies Why do successive ionisation graphs show evidence for shell structure
Within each sha;; successive ionisation energies increase because electrons are being removed from and increasingly positive ion and there’s also less repulsion amongst the examining electrons so electrons are held strongly by the nucleus Big lumps in ionisation energies happens when a new shell is broken into
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Ionisation energies How can you tell which groups and Lenten is from from a successive ionisation energy graph
Couldn’t how many electrons are removed before first big group
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Ionisation energies How can successive ionisation energy graphs be used to predict the electronic structure of an elements
Working from right to left count how many pints there are before each big jump to find how many electrons are in each shell
41
Structure bonding and properties Examples of giant covalent lattices
Diamond graphite and graphene and silicon
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Structure bonding and properties What are giant covalent lattices
Huge network of covalently bonded atoms
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Structure bonding and properties How many bonds can each carbon atom make
4
44
Structure bonding and properties What are allotropes and example
Different form so the same element in the same state eg carbon has graphite carbon and graph even
45
Structure bonding and properties What is the bonding and structure in diamonds
Each carbon is Covalently bonded to four other carbon atoms and they arrange themselves is a tetrahedral shape -crystal lattic structure
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Structure bonding and properties Properties of diamonds
Very high melting point (sublimes) Extremely hard Good thermal conductor because vibration Eason;ly travel through the stiff lattice Can’t conduct electricity Won’t dissolve
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Structure bonding and properties Reason for properties in diamonds
String covalent bonds
48
Structure bonding and properties Structure and bonding in silicon
Forms a crystal lattice structure with similar properties to carbon each silicon forms four throng covalent bonds
49
Structure bonding and properties Structure and bonding in graphite
Carbon atoms arranged in sheets of flats hexagons each carbons atom covalently bonded with three bonds each Sheets bonded together with weak London forces Fourth electron of each atom delocalised between the sheets
50
Structure bonding and properties What do the weak forces between the layers mean for graphite
Layers easily broken so the beets can slide over each other Graphite feels slippery and issued as a lubricant and in pencils
51
Structure bonding and properties Why can graphite conduct electricity
Delocalised electrons aren’t attached to any particular carbon atom and are free to move
52
Structure bonding and properties Why is graphiteused to Kate strong lightweight sports equipment
Layers are quite far apart compared to the length of covalent bond so graphite is less dense
53
Structure bonding and properties Why is graphite have a high melting point
Strong covalent bonds in hexagon sheets
54
Structure bonding and properties Why is graphite insoluble
Covalent bonds too strong to break
55
Structure bonding and properties What is graphene
Sheet of carbon atoms joined together in hexagons One atoms thick each carbon atoms makes three bonds
56
Structure bonding and properties Why can graphene conduct electricity
Delocalised electronics are free to move along the street Can move quickly above and below the sheet
57
Structure bonding and properties Why is graphene extremely strong
Delocalised electrons strengthen the covalent bonds between the carbon atoms
58
Structure bonding and properties Physical properties of graphene
Single layer makes it transparent and extremely light
59
Structure bonding and properties Potential applications of graphene
High speed electronics and aircraft technology due to high strength low mass and good conductivity Touchscreens due to flexibility and transparency
60
Structure bonding and properties Structure and bonding in giant metallic lattice strictures
Delocalised electrons electrostatically attracted yo the metal positive ions
61
Structure bonding and properties Melting point factors in giant metallic structures
Number of delocalised electrons, the more there are the stronger the bonding there will be and the higher the melting point eg MG2+ has 2 electrons per atom whereas NA+ only has 1 electron per atom to MG will have a higher melting point Size of metal ions also has impact smaller atomic radius means delocalised electrons closer to nucleus
62
Structure bonding and properties Why are giant metallic structure ductile and malleable
No bonds holding specific ions together so metal ions can slide past each other when structure is pulled
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Structure bonding and properties Why are giant metallic stricture good thermal conductors
Delocalised electrons can pass kinetic energy to each other
64
Structure bonding and properties Why are metals good conductor
Delocalised electrons can move freely and carry charge
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Structure bonding and properties Why are most metals insoluble
Because of strength of metallic bonds
66
Structure bonding and properties What affects melting and boiling points across a period
The type of bonding
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Structure bonding and properties How do you explain graph with melting or boiling point across a period
Describe type of bonding
68
Group 2- alkaline earth metals What ion do group 2 elements form
2+
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Group 2- alkaline earth metals How many electrons are in the outer shell of grp 2 elements
2 subshell (s2)
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Group 2- alkaline earth metals What stricture do group 2 ions have
Noble gas
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Group 2- alkaline earth metals What does reactivity do as you go down the group
Increases
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Group 2- alkaline earth metals Why does reactivity increase as you go down croup 2
As you go down ionisation energies decrease due to increasing atomic radii and shielding effect from inner shells
73
Group 2- alkaline earth metals What happens to group 2 element when they react
They’re oxidised From oxidation’s state 0 to +2 Lose 2 electrons
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Group 2- alkaline earth metals What do groups 2 metals react with water to form
Metal hydroxide and hydrogen gas
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Group 2- alkaline earth metals Equation for group 2 nd water
M (s). + 2 H2O (l) —> M(OH)2 (aq) H2 (g)
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Group 2- alkaline earth metals Group2 metals how they react with water
I Be -doesn’t react I Mg- VERY slowly I Ca - steadily I Sr- fairly quickly V Ba-rapidly
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Group 2- alkaline earth metals What do group 2 burn with oxygen to form
Solid white oxides
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Group 2- alkaline earth metals Reaction with oxygen equation
2 M (s) + O2 (g) —> 2 MO (s)
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Group 2- alkaline earth metals What do groups 2 react with dilute acid o form
Salt and hydrogen
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Group 2- alkaline earth metals Equation for groups 2 with dilut HCl
M (s) + 2 HCL (aq) -> MCl2 (aq) + H2(g)
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Group 2- alkaline earth metals Reactivity of group 2 with acids as you go down the group
Get more vigorous
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Group 2- alkaline earth metals What are group 2 oxides and hydroxides
Bases and mostly soluble in water therefore alkalis
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Group 2- alkaline earth metals Why are groups 2 hydroxides strongly alkaline
Hydroxide ions when in aqueous
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Group 2- alkaline earth metals Exception for solubility and alkaline in group 2
Magnesium oxide
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Group 2- alkaline earth metals Trend for group 2 oxides alkaline
Oxides form more strongly alkaline solutions as you go down the group because hydroxides get more soluble
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Group 2- alkaline earth metals What are group 2 compounds often used for
Neutralising acids Eg calcium hydroxide used in agriculture to neutralise acidic soil Eg magnesium hydroxide and calcium carbonate used in indigestion tablets
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Group 7-the halogens what are all group 7 elements
Diatomic molecules
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Group 7-the halogens What colour and state is fluorine
Pale yellow gas
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Group 7-the halogens What colour and state is chlorine
Green gas
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Group 7-the halogens Colour and state of bromine
Red brown liquid
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Group 7-the halogens Colour and state of iodine
Grey solid
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Group 7-the halogens What happens to the melting and boiling point as you go down the group
Increases
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Group 7-the halogens Why do melting and boiling points increase as you go down
Due to increasing strength of London forces as the size and relative mass of atoms increases
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Group 7-the halogens How do the physical properties show the trend of melting and boiling points down the group
The congaed of physical state from chlorine has to iodine solid- volatility decreases
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Group 7-the halogens What does volatile mean
Substance that have low boiling point
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Group 7-the halogens What happens to reactivity down the group
Get less reactive
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Group 7-the halogens What happens to halogens when they react
React by gaining and electron to form a 1- ion which means they’re reduced
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Group 7-the halogens What type of agents are they
Oxidising agents
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Group 7-the halogens Why does it get less reactive down the group
The atomic radii increases so outer electrons are further away from the nucleus, outer electron also shielded more form th attraction of the positive nucleus because of inner shields Harder for larger atoms to attract the electron needed to form an ion
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Group 7-the halogens What happens to the relative oxidising strengths
Decrease down the group
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Group 7-the halogens How can there relative oxidising strengths be seen
In their displacing reaction with halide ions
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Group 7-the halogens Full equation for Bromine reaction with potassium iodide
Br2 (aq) + 2 KI (aq) —> 2 KBr (aq) + I2 (aq)
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Group 7-the halogens Ionic equation for bromine after with potassium iodide
Br2 (aq) + 2 I- (aq) —> 2 Br- (aq) + I2 (aq)
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Group 7-the halogens What happens in the displace ment reaction to show the oxidising strengths
Colour changes
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Group 7-the halogens How can the colour changes be easily seen in displacement with halide ion
By shaking mixture with and organic solvent such as cyclohexane
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Group 7-the halogens WHaat will happen to the halogen that’s present which organic solvent is added
Settles as a distance layer above the aqueous solutions
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Group 7-the halogens What colour is KCl (aq)
Colourless
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Group 7-the halogens What colour is KBr (aq)
Colourless
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Group 7-the halogens What colour is KI (aq)
Colourless
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Group 7-the halogens What colour is chlorine water / Cl2 (aq)
Pale Green
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Group 7-the halogens What colour is bromine after / Br2 (aq)
Yellow
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Group 7-the halogens Wat colour is iodide solution/ I2 (aq)
Orange
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Group 7-the halogens What is the colour of KCl (aq) and Cl2 (aq) in aq
No reaction
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Group 7-the halogens What is the colour of KCl (aq) and Cl2 (aq) in organic solution
No reaction
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Group 7-the halogens What is the colour of KBr (aq) and Cl2 (aq) in aq and what does it show us present
Yellow Br2
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Group 7-the halogens What is the colour of KBr (aq) and Cl2 (aq) in organic. And what does it show is present
Orange Br2
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Group 7-the halogens What is the colour of KI (aq) and Cl2 (aq) in aq and what does it show is present
Orange brown I2
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Group 7-the halogens What is the colour of KI (aq) and Cl2 (aq) in organic and what does it show is ppresent
Purple I2
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Group 7-the halogens What is the colour of KCl (aq) and Br2 (aq) in aq
No reaction
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Group 7-the halogens What is the colour of KCl (aq) and Br2 (aq) in ornagic
No reaction
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Group 7-the halogens What is the colour of KBr (aq) and Br2 (aq) in aq
No reaction
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Group 7-the halogens What is the colour of KBr (aq) and Br2 (aq) in Organic
No reaction
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Group 7-the halogens What is the colour of KI (aq) and Br2 (aq) in aq and what does it show is present
Orange brown I2
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Group 7-the halogens What is the colour of KI (aq) and Br2 ( aq) in organic and what doe it show is present
Purple I2
125
Group 7-the halogens What is the colour of KCl (aq) and I2 (aq) in aq
No reaction
126
Group 7-the halogens What is the colour of KCl (aq) and I2 (aq) in aq
No reaction
127
Group 7-the halogens What is the colour of KBr (aq) and I2 (aq) in aq
No reaction
128
Group 7-the halogens What is the colour of KBr (aq) and I2(aq) in organic ic
No reaction
129
Group 7-the halogens What is the colour of KI (aq) and I2 (aq) in aq
No reaction
130
Group 7-the halogens What is the colour of KI (aq) and I2 (aq) in organic
No reaction
131
Group 7-the halogens What else are the displacement reactions useful for
Identifying solutions
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Group 7-the halogens How are displacement reaction useful for identifying solutions
Halogen will displace a halide from the solution if the halide is below it in the periodic table
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Group 7-the halogens What will chlorine (Cl2) displace
Bromide (Br-) and iodide (I-)
134
Group 7-the halogens Ionic equation from chlorine displace bromide
Cl (aq) + 2 Br- (aq) —> 2 Cl- (aq) + Br2 (aq)
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Group 7-the halogens Ionic equation for chlorine displacing iodide (I-)
Cl (aq) + 2 I- (aq) —> 2 Cl- (aq) + I2 (aq)
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Group 7-the halogens What does bromine displace
Iodide (I-)
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Group 7-the halogens Ionic equation for bromine displacing h iodide
Br2 (aq) + 2 I- (aq) -> 2 Br- (aq). +I2 (aq)
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Group 7-the halogens What does iodine displace
No reaction with F-, Cl- or Br-
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Group 7-the halogens What is used to test for halides
Silver nitrate solution
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Group 7-the halogens How do you test for halides
First add dilute nitric acid to remove ions that might interfere with the yeast then add silver nitrate solution and a precipitate is formed of the silver halide
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Group 7-the halogens Ionic equation of halide with silver nitrate solutions
Ag+ (aq) + X- (aq) —> AgX (s) ( X is Cl Br or I)
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Group 7-the halogens What does the colour of the precipitate determine
Which halide it is
143
Group 7-the halogens What colour does chloride Cl- go with silver nitrate
White precipitate
144
Group 7-the halogens What colour does bromide Br- go with silver nitrate
Cream precipitate
145
Group 7-the halogens What colour does Iodide I- go with silver nitrate
Yellow precipitate
146
Group 7-the halogens How can you be extra sure after the silver nitrate test
Add ammonia solution as they have different solubility
147
Group 7-the halogens Ammonia solution added to chlorine after silver nitrate
Dissolved in dilute ammonia solution
148
Group 7-the halogens Ammonia solution added to bromide and solver nitrate
Dissolves in concentrated ammonia solution
149
Group 7-the halogens Ammonia solution added to iodide after silver nitrate
Insoluble in concentrated ammonia solutropn
150
Group 7-the halogens What do they undergo with alkalis
Disproportionation
151
Group 7-the halogens What conditions are needed fro them to disproportionate
Cold dilute alkali solution
152
Group 7-the halogens What can make bleach
Chlorine gas and cold dilute aqueous sodium hydroxide
153
Group 7-the halogens Equation for making bleach
2NaOH (aq) + Cl2 (g) —> NaClO (aq) + NaCl (aq) + H2O
154
Group 7-the halogens What are some uses of bleach ( sodium chlorate (l) )
Water treatment Bleach paper and textiles Cleaning
155
Group 7-the halogens What happens when you mix chlorine with water
Undergoes disproportionation
156
Group 7-the halogens Eqatrion from chlorine wit water
Cl2 (aq) + H2O (l) <==> HCl (aq) + HClO (aq)
157
Group 7-the halogens What is the mixture after chlorine and water
Hydrochloric acid and chloric (l) acid
158
Group 7-the halogens What does aqueous chloric (l) ionise too and how does it treat water
Ionises to chlorate(l) ions also called hypochlorite ions which kill bacteria making water safe to drink and swim in
159
Group 7-the halogens Strength of using chlorine to water
Kills bacteria
160
Group 7-the halogens Risks of chlorine to water
Toxic
161
Group 7-the halogens Alternatives of chlorine to water
Ozone O3 (string oxidising agent kills microorganisms) Ultra violent light- kill’s microorganisms damaging there DNA
162
Testing for ions How do you test for carbonate ions
Add dilute HCl or HNO3
163
Testing for ions What will the result be form the carbonate test of the carbonate ions are present
Carbon dioxide will be released and effervescence
164
Testing for ions Testing for ions Ionic equation for carbonate test
CO3 2- (s) + 2H + (aq) —> CO2 (g) + H2O (l)
165
Testing for ions What is the test for sulfate ions
Add dilute HCl or HNO3 followed by barium chloride solution BaCl2
166
Testing for ions Why is barium chloride used to test for sulfates
Most sulfates are soluble in water but barium sulfates is insoluble
167
Testing for ions What will be the result to show the presence ofsulfate ions
White precipitate will be formed
168
Testing for ions Ionic equation for sulfates test
Ba 2+ (aq) + SO4 2- (aq) —> BaSO4 (s)
169
Testing for ions What is the test for halide ions
Add nitric acid followed by silver nitrate
170
Testing for ions Results if chloride ion present
White precipitate and soluble in ammonia
171
Testing for ions Result if bromide ion present
Cream precipitate and only soluble in concentrated ammonia
172
Testing for ions Results if iodide ions are present
Yellow precipitate and not soluble in ammonia
173
Testing for ions What is the test for ammonium ions
Add sodium hydroxide and gently warm
174
Testing for ions Result for if ammonium ions are present
Damp red litmus paper will turn blue
175
Testing for ions Ionic equation for ammonium test
NH4 + (aq) + OH - (aq) —> NH3 (g) + H2O(l)
176
Testing for ions What order should you plan tests
If present o ammonium, then carbonate , then sulfates, then halides
177
Periodicity What happens to atomic radius across periods
Decreases
178
Periodicity Why does atomic radius decrease across groups
Outer electrons in same shell so same amount of shielding but more protons in nucleus Stronger attraction between nucleus and outer shell electrons so pulled closer to nucleus
179
Periodicity What happens to electronegativity across periods
Increases
180
Periodicity Why does electronegativity increase across periods
More protons in nucleus Smaller atomic radius Stronger attraction between nucleus and pair of electrons in the covalent bond
181
Periodicity What happens to melting and boiling points across periods
Varies
182
Periodicity How is variance in melting and boiling points across periods explained
By type of bonding and structure
183
Periodicity Explain trend in melting and boiling point across period using period 3 (long)
{Na,Mg,Al} mp,bd increases because metallic bonds, strong attraction between metal ions and delocalised e-, Al>Mg>Na because higher charge ion,more delocalised e-, smaller ions {Si} mp,bp highest on period as giant covalent structure, strong covalent bonds require lots of energy to break {P4,S8,Cl2} mp,bp increase from P to S then decrease because simple covalent molecules with weak London forces between molecules, S8>P4>Cl2 because bigger molecules have bigger molecules bigger electrons and larger IMF {Ar} lowest as very weak London forces because monatomic atoms