module 3 - periodic table and energy Flashcards

1
Q

what columns make up the S block

A

the two leftmost columns,
note - helium is also an S block element because it has the electron configuration 1s2

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2
Q

where is the P block on the periodic table?

A

the six rightmost columns
called p-block because elements in the p block have a partially filled p sub-shell

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3
Q

where is the d block on the periodic table?

A

lies between the s and p blocks, elements are often transition metals

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4
Q

where is the f block in the periodic table
what are the elements in these blocks referred to?

A

detached along the bottom of the table.
elements have a partially filled F sub-shell
elements referred to as the lanthanides and actinides (top and bottom row)

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5
Q

which element is an s block element that does NOT sit on the left-hand side?

A

helium

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6
Q

define first ionisation energy

A

the energy required to remove and electron from every atom in a mole of atomic gas, to produce a mole of unipositive gaseous ions

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7
Q

what is the second ionisation energy

A

the energy required to remove an electron from every ion in a mole of unipositive gaseous ions to produce a mole of dipositive gaseous ions

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8
Q

what is the equation for ionisation energy in terms of n

A

X^(n-1) + energy –> e- + X^n+

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9
Q

in ionisation equations, what state symbol do all the atoms/ ions have?

A

g (gas)

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10
Q

what factors effect ionisation energies

A

nuclear charge - the number of protons in the nucleus - the more protons, the greater the ionisation energy
distance from nucleus - less energy needed to remove electrons that are further away
shielding - greater the number of electrons, the lower the ionisation energy

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11
Q

what is the pattern for increasing ionisation energies

A

the n=1 shell has a higher ionisation energy than the n=2 shell.
within the n=2 shell, successive ionisation energies will rise as the ion becomes more positively charged

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12
Q

what is the lowest ionisation energy of sodium

A

first ionisation energy

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13
Q

break down the trend of the sodium atom
electron configuration = 1s2 2s2 2p6 3s1

A

first ionisation energy corresponds to the removal of an electron from the n=3 shell

the second ionisation energy corresponds to the removal of an electron from the n=2 shell

between the third and ninth ionisation energies, an electron is being removed from the n=2 shell of an increasingly positive ion

its tenth ionisation energy corresponds to the removal of an electron from the n=1 shell

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14
Q

what is the ionisation energy trend across a period

A

first ionisation energy increases across a period
because the atomic radius decreases, proton number increases across a period so electrons are more attracted to the nucleus. nuclear charge increases across a period

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15
Q

what trends do ionisation energies follow down a group

A

first ionisation energy decreases down a group because atomic radius increases
more electrons between the nucleus, so experiences lower attraction

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16
Q

what would you see when magnesium solid reacts with an excess of dilute HCl

A

you would see rapid bubbles/ effervescence and the magnesium would dissolve

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17
Q

write the ionic equation for the reaction of magnesium and hydrochloric acid

A

Mg(s) + 2H^+(aq) –> Mg^2(aq)+ H2(g)

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18
Q

describe the trend in ionisation energy down group 2

A

ionisation energy decreases as you go down as electron shielding increases, increasing the atomic radii and making the valence electrons less attracted to the positive nucleus. therefore easier to lose an electron

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19
Q

why is the second ionisation energy higher than the first?

A

because the second ionisation energy removes an electron from a positive (1+) ion, which has increased nuclear charge, so less easy to lose an electron

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20
Q

why does Al have a higher boiling point than Mg

A

because Al has a higher atomic number and therefore more electrons, increasing the electrostatic attraction between the delocalised electrons and nucleus. Al forms 3+ ions whereas Mg forms 2+ ions, therefore the bond energy is higher in Al

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21
Q

how do you work out the amount of energy required to turn an atom into a 2+ ion?

A

the first ionisation energy + the second ionisation energy

22
Q

as you go down group 2 (Mg, Ca, Sr, Br) what is the trend in reactivity with water

A

more vigorous reaction

23
Q

down group 2, what is the trend in thermal stability (carbonate)

A

more stable

24
Q

down group 2, what is the trend in solubility of OH-

A

increase in solubility

25
Q

down group 2, what is the trend in the pH of OH-

A

more alkaline

26
Q

down group 2, what is the trend in carbonate solubility

A

decrease in solubility

27
Q

how do you test for halides?

A

add dilute nitric acid - reacts and removes any carbonates
add silver nitrate, AgNO3 (aq)

28
Q

what are the results when you test for the halides
chloride
bromide
iodide

A

chloride = white precipitate
bromide = cream precipitate
iodide = yellow precipitate

29
Q

what state is sodium salts always in when in a reaction?

A

aqueous (always soluble in water)

30
Q

as the chloride’s white ppt and bromide’s cream ppt appear very similar, how can you differentiate between the two

A

add dilute ammonia (NH3)
- chloride white ppt dissolves (white solution)

then add concentrated ammonia (NH3)
- bromide cream dissolves (cream solution)
- iodide yellow does not dissolve (ppt)

31
Q

define disproportionation

A

a reaction in which a substance is simultaneously oxidised and reduced to form different products

32
Q

write the equation for sodium bromide and silver nitrate
what type of reaction is this?

A

NaBr (aq) + AgNO3(aq) –> AgBr(s) + NaNO3(aq)
displacement reaction

33
Q

what type of molecules are halogens

A

diatomic molecules
Cl2
Br2
I2

34
Q

when you add cyclohexane to the halogens
chlorine
bromine
iodine
what colour is observed in the water layer and in the Volasil layer

A

chlorine = water = almost colourless, volasil = almost colourless

bromine = water = orange, volasil = red-brown

iodine = water = red-brown, volasil = purple

35
Q

define enthalpy change

A

a measure of the heat given out or taken in during a process

36
Q

why is enthalpy preferred over energy change

A

because energy change has to have a fixed volume, whereas enthalpy takes into account the expansion when objects are heated

37
Q

what pressure is enthalpy change measured under

A

always constant atmospheric pressure - constant

38
Q

energy is required to … a bond - …thermic

A

break a bond - endothermic

39
Q

energy is released when a bond is … - … thermic

A

made - exothermic

40
Q

define dominating term in bond enthalpy

A

whether the reaction requires more energy to break the bonds or to make bonds - overall is either positive or negative

41
Q

how do you calculate the overall enthalpy

A

add together the enthalpies of breaking bonds and minus the enthalpies for making bonds

42
Q

if the overall enthalpy of a reaction is negative, is the reaction more endothermic or exothermic

A

exothermic (energy is released to make bonds)

43
Q

how do you remember the correlation between exothermic and endothermic, bond making and bond breaking

A

Bendo-Mexo
break = endo
make = exo

44
Q

what are the standard conditions for enthalpy changes

A

pressure = 1Bar
temperature = 298 K (kelvin)

45
Q

define the bond enthalpy of standard combustion

A

the enthalpy change when one mole of a substance in its standard state burns completely under standard conditions

46
Q

define the bond enthalpy of standard formation

A

the enthalpy change when one mole of a substance is formed in its standard state from the pure elements in their standard states, under standard conditions

47
Q

why and how do you work out the mean enthalpy change

A

why? some molecules have multiple identical bonds but the second bond enthalpy will be greater than the first as the molecule rearranges after the first bond breaks. therefore a mean is more accurate

how? work out the average of all the bond enthalpies in a molecule

48
Q

what are the inaccuracies of the mean enthalpy change

A

means are only valid in the gas phase (reaction might not occur in this phase

bond enthalpies depend on the particular molecule, whereas mean bond enthalpies are quoted generally

49
Q

what is Hess’ Law?

A

the enthalpy change is independent of the pathway
means the change is the same whether the reaction is direct or indirect

50
Q

how does Hess’ Law help us work out bond enthalpies

A

helps us use smaller, easier reactions to work out the bond enthalpies of more obscure reactions
eg. A-> B -> C-> D -> E = A->E

51
Q

what is the equation for Hess’ cycle

A

delta H1 + delta H2 = delta H3