SEM 1 EXAM Flashcards

1
Q

how does nucleus stay together

A

electrostatic repulsion forces protons apart, but strong nuclear force attracts nuclear particles together
if nuclear force is balanced, atoms is stable

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2
Q

what happens if nuclear forces are unbalanced

A

then the nucleus will be unstable and decay over time

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3
Q

isotopes

A

atoms of an element with the same number of protons, but different number of neutrons.

chemical properties are similar (atom behaviour in chem reaction is based on arrangement and number of electrons.

different physical properties (mass and nuclear stability)

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4
Q

chemical and physical properties

A

how elements participate in chemical reaction

feature one can measure and observe

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5
Q

radioactive decay of isotopes

A

if forces in atom are balanced, atom is stable
if not balanced, atom is unstable and nucleus undergoes radioactive decay to become stable.

in radioactive decay, radiation is emitted, which is useful for radioactive dating and medical diagnosis and treatment

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6
Q

half-life

A

time taken for half the original sample to decay

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7
Q

relative atomic mass

A

compares the mass of atom to the mass of another atom
all atoms are compared to carbon 12
isotopes have different masses and abundances on earth

weighted average of the relative masses of the isotopes of an element relative to carbon12

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8
Q

Democritus

A

disagreed with the idea of infinitely divisible matter, proposed that matter consisted of tiny particles with nothing between them but empty space called “atomos”

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9
Q

dalton

A

elements composed of atoms
an atom of same element have a same properties, atoms of different elements have different properties
atoms not created nor destroyed or changed into different types during reactions
c reaction is separation, combination , rearrangement of atoms
compounds are combinations of atoms in specific ratio

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10
Q

thomson

A

found electrons

realised that atoms could be divided further

plum pudding model: electrons embedded in positively changed mass

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11
Q

rutherford

A

proposed the atom consisted mostly of empty space

electrons orbited around nucleus. most of mass was in the nucleus, all positive charge was located in the nucleus carried by protons

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12
Q

bohr

A

electrons were in electrons shells around the nucleus, each shell has a specific amount of energy

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13
Q

Chadwick

A

discovered the existence of neutrons that accounted for around half the mass of the nucleus, had neutral charge

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14
Q

Electrostatic attraction

A

related to distance the valence electrons are from the nucleus

strength of attraction of protons and electrons

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15
Q

shielding effect

A

related to number of inner shell electrons, shield the effect of the protons from valence electrons.
reduces ionisation energy

correlates to number of inner electron shells and attraction of valence electrons to nucleus

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16
Q

core charge

A

how defective the charge of the nucleus is at holding the valence electrons in

increases going towards noble gases

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17
Q

atomic radii

A

decrease going right

increase going down

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18
Q

electronegativity

A

ability of atom to attract electron
increases going right
decrease going down as electron is further from nucleus so it is harder to attract

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19
Q

ionisation energy

A

energy required to remove loosely bound electron
depends on
nuclear charge: more nuclear charge means more protons in nucleus which increases ionisation energy because valence electrons are tightly held on.
distance form nucleus: further distance decreases electrostatic attraction between valence electrons and nucleus. valence electrons are loosely held.

increases towards right
decreases going down because valence shell is further away making it easier to lose electrons

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20
Q

electron affinity

A

ability to accept electron and from a negative ion

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21
Q

metallic character

A

set of properties associated with metals

depends on ability to lose valence electrons

decrease going right
increase going down

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22
Q

ground state

A

shells next to nucleus are taken up by electrons

when electron is at its lowest possible energy levels

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23
Q

how electrons jump

A

atoms absorb energy, electron around nucleus gain this extra energy and move up to higher energy levels.
electrons can be so excited that they leave (ionisation)

energy levels are discreet. electrons can only exist in specific energy levels
electrons cannot exist between energy levels, therefore

amount of energy absorbed and emitted = difference in one energy level and another. electrons could be excited from one energy level to another by specific amounts of energy that corresponds to the difference in energy levels.

amount of energy absorbed by any sample of one element is the same

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24
Q

excited state

A

an atom in which electrons occupy higher energy levels than the lowest possible energy levels.
as it moves back to ground state, emits light

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25
Q

atomic emission spectroscopy

A

absorption and emission of light help identify element
process of analysing light emitted by electron as it return to ground state

spectroscope: takes emitted light and separates it into its component wavelengths to produce a line emission spectrum.

sample to analysed is heated to much higher temperatures, and light emitted is passed through a prism. the prism disperses light into its component colours. the monochromatic allows single wavelengths to pass at a time, then spectra is recorded

fingerprint

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26
Q

AAS

A

uses absorption of light by electrons to measure how much of an element is present. used AAS

  1. element analysed is determined: there could be many element in a sample but we need to focus on one. thus the lamp is made of the same element being tested. current passes through gaseous sample of element in lamp and emits light. has unique wavelengths to other elements
  2. vaporised: changing substances in sample to atoms. when light passes through, only the element being tested will absorb the light because it has the same energy levels as atoms that emitted light from lamp.
  3. detection: light passed through sample enters monochromator-> selects one wavelength of light for analysis by detector-> measures intensity of light and turns it into a number.

compared to known samples by constructing a calibration curve. concentration against absorbance value.

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27
Q

absorbance value

A

measure of amount of light that passed through sample without being absorbed, lets you know concentration

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28
Q

what is mass spectrometry

A

based on different masses of atoms in sample

determine what elements are present in a sample or what isotope and their abundance in a sample.

determines mass relative to carbon12 and calculates relative abundance of the isotope

determine isotopic composition of an element.

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29
Q

method of mass spectrometry

A

sample vaporised then…
1. ionisation: sample is bombarded with high energy electrons/ UV LIGHT.
removes valence electrons leaving atom with positive charge
does this with ALL atoms.

  1. acceleration: cations accelerated through electrical field at very high speeds according to mass-charge ratio
  2. deflection: pass through a magnetic field where they undergo deflection according to their mass. ions separated according to mass and charge
    lighter= more deflection
  3. detection: detectors measure amount of ions that strike them
    graphed in a mass spectrum.
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30
Q

why does lamp pulsate in atomic absorption spectroscopy

A

light from the lamp is pulsed so that the detector can distinguish between the light from the cathode lamp that is left over after absorbance and the continuous light naturally emitted gaseous atoms in the flame/burner returning back to their ground state.

finds extent of lamp light being absorbed and to what extent

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31
Q

material

A

substances that make other objects. often mixtures of many substances. can be pure (elements and compounds)

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32
Q

pure substance

A

Pure substances are defined as substances that are made of only one type of atom or molecule.
properties cannot be altered
distinct and measurable properties for any given arrangement of atoms or molecules

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33
Q

pure substance vs homogeneous mixture

A

homogeneous mixture: components can be separated

pure substances: can’t be separated

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34
Q

elements

A

substances made of one type of atom

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35
Q

compounds

A

pure substance made up of more than one type of atoms

chemically combined, uniform composition

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36
Q

pure substances

A

properties cannot be altered. properties are distinct and measurable for any given arrangement of atoms or molecules

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37
Q

mixtures

A

properties can be changed depending on how much of each component is added mixture.this useful as properties can be controlled.

individual components keep their properties
variable composition

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38
Q

alloy

A

mixture of metal with other metals or small amount of non metals

e.g. iron is soft an sprone to corrosion. but adding some carbon creates steel which is stronger and corrosion resistant

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39
Q

polymer

A

material with a molecular structure that is composed of many repeating smaller units bonded together.

compared to metals, they are less dense, electrical insulator, corrosion resistant

natural: wool, silk, paper
synthetic: polystyrene

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40
Q

ceramics

A

inorganic, non metallic solid. composed of metals, nonmetals, metalloids held together by ionic and covalent bonds.
can be highly ordered (crystalline)or highly irregular (amorphous)

natural: kaolinite (makes porcelain)
synthetic: silicon carbide (used as an abrasive)

properties: hard, high compressive strength, able to withstand high temperatures. most are good insulators, but some have semi/super conducting properties

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41
Q

composite materials

A

combination of two or more distinct materials with significantly different chemical and physical properties.

creates a range of properties that would be unobtainable with using one of the individual components.

e.g. reinforce concrete = concrete matrix +embedded steel bars
low tensile strength of concrete counteracted with high tensile of steel
maintains high compressive strength of concrete

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42
Q

heterogenous mixture

A

non uniform mixtures that contain physically separate materials
not pure or uniform
mixtures can have different proportions of the same components .

eg. granite has 3 different minerals, each piece has a different amount but it is still granite

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43
Q

homogenous material

A

materials that have uniform composition throughout

breaking it smaller = would be identical

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44
Q

homogenous solution

A

consists of solute and solvent, solute is distributed throughout the solvent as very small particles, so it appears uniform

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45
Q

nanoscale

A

structure between 1 and 100 nm

nanometer = 10 ^-9

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46
Q

nanomaterial

A

substances (natural and synthetic) that are composed of single units that exist in ten nanoscale

very large surface area compared to the volume they occupy

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47
Q

adsorption of nano-materials

A

where molecules stick to surface of of a solid or liquid
can be used to remove unwanted chemicals and gases
large surface area means that a small volume of nanoparticles can adsorption a large number of molecules

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48
Q

transportation of nano materials

A

can transport molecules that are adsorbed

small size and large surface area mean that they can transport chemicals through air, skin and even cells

used in chemotherapy treatments for cancer as it can transport drugs to specific cells

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49
Q

nano materials as catalysts

A

can speed up rate of reaction without being altered or destroyed in the process. provide surface for reaction to occur

reactant molecules absorb onto the surface of the nanoparticles which allows reactant molecules to combine to form the product

large sa means many reactions can occur at once. ->increases rate of reaction

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50
Q

gold as nanoparticles

A

properties can change as nanoparticles

gold changes its colour
melt at lower temperatures and appear red in solution

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51
Q

zinc oxide in sunscreen

A

good absorbers of uv radiation and appear transparent because the particle size is much smaller than the wavelength of visible light, so light can go through it with very little being affected

other metal oxides tend to be milky white

having nanoparticles means that it’s distributed evenly so uv radiation is absorbed/scattered by zinc oxide. if they were bigger it means that it wouldn’t be evenly distributed and up rays could pass through

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52
Q

Nanoparticles in medicine

A

colloidal gold: labeling antigens, optimises distribution of drugs to cells in difficult areas (brain, retina, tumours), targets tumors and provides detection

silver: antibacterial and antifungal properties, due realease of silver ion from surface of metal
sa enhances antibacterial effectiveness

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53
Q

safety risks of nanoparticles

A

can travel through air, bloodstream, skin, cells

can interact with inside body (biomolecules) to cause unwanted reactions

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54
Q

composite nanomaterial

A

small size and unique properties are useful for them to be composite nanoparticles

stain resistant cotton: cotton fibres covered with water resistant nanoparticles

tyres: added carbon improved resistance and abrasion. increase electrical conductivity, prevents build up of static electricity

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55
Q

fullerenes

A

3d structures formed by networks or carbon atoms

nanotube: cylindrical tube, reinforcement in composite nanomaterial
graphene: flat 2d layer of carbon atoms arranged in hexagons
buckyball: soccer ball shaped 3d structure

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56
Q

top down method to make nanoparticles

A

size of material is progressively reduced , by grinding until size is achieved.

+: large quantities produced, cheap, uniform

-: limited to simple structures

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57
Q

sieving

A

based on particle size

separates mixtures of different particles, smaller particles pass through holes, large ones are trapped

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58
Q

filtration

A

particles not dissolved in solvent

separates suspended solid from a liquid using a filter funnel and paper.

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59
Q

Evaporations

A

particles dissolved in liquid

boiling/evaporating solvent away from solute

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60
Q

distillation

A

differences in boiling point
separates two liquids with different boiling points or a soluble solid and the solvent

distillation flask, condenser, receiving flask

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61
Q

fractional distillation

A

vapour passes through a column packed with glass beads. less volatile component component condenses on the glass beads and drips back to distillation flask

can be used to separate miscible liquids

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62
Q

separating funnel

A

difference in density
immiscible liquids separate into layers due to density

tap is opened to let the more dense component out of the mixture

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63
Q

metallic bonding

A

chemical bonding that results from attraction between metal atoms and the surrounding sea of electrons
metals have low ionisation energy that is why they lose electrons easily

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64
Q

high MP and BP of metals

A

forces of electrostatic attraction between metal cation and delocalised electrons are very strong so it requires more energy to break them

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65
Q

why do metals conduct electricity

A

delocalised electrons are free to flow through the metal and so carry a current.

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66
Q

why are metals malleable

A

bonding in metals is not rigid. as metals are metal with a force, the atoms slide through electron sea to new positions while continuing to maintain their connections to each other. this also makes the ductile.
attractive forces stronger than repulsive.
non directional bonding

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67
Q

why are metal dense

A

particles are closely packed together

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68
Q

why are metals shiny and opaque

A

freely moving and delocalised electrons are present so metals can reflect light and appear shiny.
close packing of cations prevent light from slipping through making it opaque

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69
Q

what does a greater core charge in a metal mean in terms of bonding

A

atoms packed tightly with stronger bonds

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70
Q

metallic bond structure

A
  1. cations are closely packed in 3d network. cations occupy fixed positions in lattice
  2. delocalised electrons moving freely. they belong to the lattice as a whole, not an individual atom
  3. these electrons come from valence electrons not inner shell ones
  4. cations held in position due to ESF of attraction between cations and electrons (metallic bonding)
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71
Q

limitations to metallic bonding

A
structure can't explain:
variations in properties
magnetic nature
differences in electrical conductivities
*more complex model needed
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72
Q

ways to modify metals

A

alloy production
heat treatment
formation of nanoparticles

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73
Q

metal alloys

A

mixing metals with other substances (metal/carbon). substances are melted, mixed and cooled.

harder and lower MP: since atoms of different sizes are now included, the properties may differ. lattice doesn’t move in the same way (lower MP)

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74
Q

iron and carbon

A

steel
harder and less corrosive, but less malleable because atoms are slightly different in size and lattice can’t move past each other as easily.

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75
Q

ionic bonds

A

when a metal and non metal come into contact and a electron is lost from the metal and given to non metal. cations and anions formed. held together by electrostatic forces of attraction between ions (ionic bonding)

ions have inert gas electron configuration

each cation is surrounded by anion and vice versa (attractive forces outweigh repulsive forces)

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76
Q

high MP and BP of ionic bonds

A

large amount of thermal energy to overcome attraction between oppositely charged ions and allow them to move freely
bricks in furnace made of MgO

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77
Q

why are ionic compounds brittle and hard

A

strong forces of electrostatic attraction hold ions together, so a strong force is required to break them
brick in houses CaPO4

when a force is applied ions move in the direction of the force, like ions are forced together causing them to repel (repulsion causes it to shatter)

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78
Q

ionic compounds and electrical conductivity

A

solid: not free to move, can’t conduct current
ceramic insulators

solution/liquid: lattice dissociates in water into charged ions that move freely in solution
cations -> cathode
anions -> anode
ammonium chloride in dry cell batteries as electrolytes

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79
Q

ionic compounds and solubility

A

soluble: ions break away and mix with water molecules
insoluble: ions remain bonded and don’t form a solution
depends on:
1. attraction between cation and anion
2. ion and water molecule

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80
Q

why are metals good conductors of heat

A

cations vibrate vigorously and are able to transfer thermal energy to each other
delocalised electrons readily transfer thermal energy as they move through the lattice

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81
Q

why do metals form cations

A

low ionisation energy

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82
Q

interstitial alloy

A

when atoms of element that is supposed to be mixed with metal is much smaller and fill spaces between lattice

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83
Q

Substitutional alloy

A

larger, similar property metal added to lattice

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84
Q

covalent molecular bonds

A

sharing of electrons to attain full valence shell. molecules are discrete (individual)
if atoms have similar electronegativities than they are like to form covalent bonds because they have the same affinity for electrons and don’t want to donate.

positively charged nuclei attracted to shared electrons

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85
Q

low MP of covalent molecular bonds

A

Intermolecular forces are weak so not much energy is required to break them

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86
Q

non conductive of covalent molecular

A

no mobile particles

electrons locked in covalent bonds

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87
Q

softness of covalent molecular

A

intermolecular forces are weak
molecules can be moved out of position easily
hence soft

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88
Q

covalent networks and properties

A
only intramolecular forces
made form network of repeating lattices of covalently bonded atoms (intramolecular)
eg silicon dioxide, carbon, silica
properties: 
hard
high MP + BP
solid @room temp
non conductive (except graphite)
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89
Q

allotrope

A

different forms of an element
atoms bonded together in different specific ways
have slightly different properties

90
Q

diamond

carbon allotrope

A

hard -> not discrete in covalent network lattice
each carbon surrounded by 4 other carbon
high thermal conductivity because atoms are held together strongly

91
Q

graphite

carbon allotrope

A

slippery, soft, greasy
conductive (free moving electrons)
covalent layer lattice ( each carbon has 3 other carbons and 1 delocalised electron per carbon atom)
each sheet is slightly positive and pushes down electrons which means there is weak attraction.

92
Q

% composition

A

how much M, m, n of each element make up the total chemical

93
Q

Properties of gas

A
can be compressed
diffuse
low density
no fixed shape or volume (diffuse)
measured by volume in L
94
Q

things that affect behaviour of gases

A

temp
high temp = high energy
increasing temp increases volume and pressure if volume is kept the same

pressure (kPa)
increase in pressure decreases volume and increase temp as particles now have higher energy

volume (space taken up by gas)
increase in volume decreases pressure and temperature because of lower energy and less collision as particles are further apart

95
Q

relationship between volume and pressure at a constant temp

Boyles law

A

inversely proportional
as one increases, the other decreases
bike pump example

96
Q

STP

A

standard temp and pressure

t: 0ºC or 273.15ºK
p: 100 kPa

1 mol of any gas at STP will occupy 22.71 L

97
Q

flame test procedure

A
  1. Place a small amount of salt in a clean watch glass.
  2. Add to 1-2 mL of ethanol to the sample and stir with a toothpick
  3. Place the watch glass on a heat proof mat
  4. Carefully light the ethanol
  5. When the flame burns low observe the colour produced
  6. Repeat for each salt using a clean watch glass each time
98
Q

examples of things that aren’t materials

A

chemicals like: HCl, chlorophyll, carbon dioxide

99
Q

sedimentation

centrifugation

A

gravitational separation, pouring of liquid from undissolved settled solid

speeds up sedimentation by spinning very quickly, even very small dissolved solids are settle

100
Q

solutions and compounds are both?

A

homogenous
solutions can be physically separated because its not chemically bonded, just dissolved. however it does have a uniform composition
Solutions consists of solute dissolved in solvent

101
Q

why do nanomaterial properties change

A

as they become smaller, surface area to volume ratio increases which changed properties because majority of properties occurs at the surface

102
Q

non octet covalent molecules

A

Be and B are small atoms with only 2 and 3 electron pairs, because it is small enough, arrangements are stable enough for molecules to still form without following octet rule.
boron has 3 valence, but still makes BF3, now has 6 valence, molecule forms even though it doesn’t follow octet rule.

P and S are larger atoms that can accomodate 5 or 6 bonding pairs

103
Q

kinetic energy and gas

A

KE can be transferred from one particle to another but the total KE remains the same
collisions between gas particles are elastic collisions, KE is conserved

104
Q

pressure (gases)

A

force exerted on surface by gas particles as they collide with the surface
force/area

105
Q

uses of AES

A

analyse metallic elements in solid samples

analyse trace elements in soil, water ,etc

106
Q

uses of AAS

A

identify toxic metals in urine or blood
pollutants in soil or water
quantity an prescience of precious metals such as gold and silver

107
Q

uses of MS

A

drug testing and discovery

food contamination detection

108
Q

sample of hydrogen atoms absorbing light

A

if exposed to continuous spectrum of visible light, hydrogen will only absorb certain colours, these colours have energies that perfectly correspond to energy needed for electron to move up energy levels.
dark lines are colours absorbed

109
Q

why are there several absorption/emission lines, if hydrogen only has 1 electron

A

spectrums represent the collective emissions of many individual hydrogen atoms

110
Q

chemical reactions

A

when particles collide and are rearranged to form new particles. chemical reactions involve energy changes.
as the reactant particles are rearranged, the chemical energy of the reactants is changed also.
energy can be absorbed or released

111
Q

chemical energy

A

stored in chemical bonds between atoms and molecules. energy results from:
attractions between electrons and protons
repulsion between nuclei
repulsion between electrons
movement of electrons
vibration and rotation around bonds

112
Q

law of conservation of energy

A

states energy cannot be created or destroyed.
chemical energy stored in a substance reduce and the energy must go elsewhere
a substance can’t gain in chemical energy without absorbing that energy from another source

113
Q

system

A

the chemical reaction

refers to energy changes that occur as bonds and formed between the atoms of the elements involved in the reaction

114
Q

surroundings

A

everything but the chemical reaction

energy goes from the surrounding to the reaction or energy is released into the surroundings

115
Q

energy changes

A

the reactants in a reaction have a certain amount of energy in bonds, since the products are a rearrangement of the particles so they have different bonds and thus different amount of energy
for particles to separate,

energy is required, the separated articles have more energy than when they were together. particles coming together the products will have less energy than the separate particles, this lost energy is transferred to the surroundings

116
Q

specific heat capacity

A

energy needed to change temperature of 1kg of a substance by 1 degree

117
Q

exothermic

A

energy of products is less than energy of reactants and the lost energy is transferred to its surroundings

118
Q

endothermic

A

when energy of the products is greater than the energy of the reactants
energy is absorbed from the surroundings

119
Q

melting or boiling

A

endothermic

120
Q

freezing

A

exothermic

121
Q

activation energy

A

energy required to break the bonds of reactants so that a reaction can proceed
energy barrier that must be overcome before a reaction can start
unless this minimum energy amount is met, reactants rebound and move away from each other without reacting

122
Q

combustion

A

the release of chemical energy when the fuel is burnt in the presence of oxygen
exothermic

123
Q

complete combustion

A

when oxygen is plentiful and products are carbon dioxide and water

124
Q

incomplete combustion

A

when oxygen supply is limited

not all carbon can be converted into carbon dioxide so carbon monoxide and or carbon is produced instead

125
Q

energy content of fuels

A

heat of combustion of a fuel is defined as enthalpy change when a specified amount of fuel burns completely in oxygen
energy content: chemical energy available from a substance
fuels have high energy contents

126
Q

factors that affect reaction rate

A
surface area of solid reactants
concentration of reactants in a solution
gas pressure
Temperature 
presence of catalysts
127
Q

rate of reaction

A

change in concentration of a reactant or product per unit time
need to measure amount of product being formed or amount of reactants being used up in a given ti8me period
depends on activation energy
magnitude of activation energy determine how easy it is for a reaction to occur and what proportion of collisions result in a successful reaction

128
Q

collision theory

A

for collision theory to occur reactant particles must
collide with each other
collide with each other with sufficient energy to break bonds between the reactants
collide with the correct orientation to break the bonds between reactants and so allow formation of new products, if not correct orientation, particles bounce off each other

129
Q

transition state

A

a new arrangement of atoms when activation energy is absorbed
occurs at the stage of maximum potential energy in the reaction (activation energy)
bond breaking and forming occur at this stage and arrangement of atoms is unstable

130
Q

increase reaction rate

A

increasing a number of collisions that can occur in a given time
increasing proportion of collisions with an energy equal or greater than the activation energy

131
Q

increasing frequency of collisions

A

increasing concentration of reactants (increasing pressure increase concentration)
increasing surface area of a reactant (more particles, more exposed surfaces of particles )
increase pressure

132
Q

increasing energy of reactions

A

increasing temperature

catalyst lower activation energy required

133
Q

importance of shape of molecule

A

affects vapour pressure, melting point, boiling point and solubility. shape determines how it interacts with other molecules

134
Q

VSEPR

A

uses knowledge of valence shell to predict shape
based on principle that negatively charged electron pairs in valence shell repel each other. meaning that these electrons are arranged as far away from each other as possible
electron pairs in the single covalent bonds repel each other
lone pairs are treated the same as electron pairs in covalent bonds because they still take up space int he atom
double and triple bonds are treated as a single bond

135
Q

tetrahedral (methane)

A

electron pairs in the single covalent bonds repel each other
repulsion forces the bonds as far apart from each other as possible, so hydrogens are arranged in a tetrahedral shape at an angle of 109.5º

136
Q

pyramidal (ammonia)

A

lone pairs are treated the same as electron pairs in covalent bonds because they still take up space int he atom
3 hydrogen atoms for a pyramidal shape with the nitrogen. the ,one pair occupies more space because it isn’t covalently bonded to a and is therefore closer to the nitrogen. this means that the 3 covalent bonds are pushed closer together making the angle less than 109.5º

137
Q

trigonal planar (water)

A

2 lone pairs and 2 covalent bonds
4 electron pairs repel each other and 2 hydrogen atoms for a v shape with the oxygen. because of the two lone pairs the 2 covalent bonds are pushed closer together
angle around central atom less than 109.5º
120º

138
Q

linear (HF)

A

fluorine has 3 lone pairs and 1 covalent bond
four pairs form a tetrahedral arrangement due to mutual repulsion
results in a linear model
180º

139
Q

BH3

BeH2

A

3 electron pairs, no lone pairs
trigonal planar

2 electron pairs, no lone pairs
linear

140
Q

strength of intermolecular forces

A

covalent molecular forces have lower melting and boiling points because forces BETWEEN molecules are weaker. these forces are disturbed when covalent substance change state

141
Q

vapour pressure

A

pressure that gaseous molecules exert on the closed container walls when the rates of evaporation and condensation become equal

liquids with stronger intermolecular forces have lower vapour pressure molecules are held together tightly making it harder for them to escape from the surface of the liquid

increasing temp increase vapour pressure. molecules have a higher average kinetic energy that enables them to overcome intermolecular forces. as temperature increases, more particles have enough energy to escape from liquid to gas. increasing pressure

142
Q

boiling point of a liquid

A

temperature at which the liquids vapour pressure reaches the atmospheric pressure of the surroundings

143
Q

electronegativity and polarity

A

in intermolecular forces, the electrostatic attraction is between positive and negative charges in the molecules
charges result because of uneven electron distribution within molecules
electronegativity is the tendency of an atom in a covalent bond to attract electrons
in a covalent bond atoms are competing for electrons being shared between them

144
Q

non polar diatomic molecules

A

when atoms have identical electronegativities, then electrons are shared equally between them. non polar because there is no charges on either end
even distribution of valence electrons between atoms
if electronegativities between atoms are very similar, then it can be considered non-polar

145
Q

electron density

A

measure of the probability of an electron being present at a particular location within an atom

146
Q

polar diatomic molecules

A

2 atoms with different electronegativities, electrons stay closer to the most electronegative atom because they are more strongly attracted to that atom
polar: imbalanced electron distribution. has two oppositely charged poles
all diatomic with different atoms are polar to some extent, greater difference in electronegativities the greater the polarity

147
Q

delta

A

partial charge, adding up partial charges = 0 because charge are due to uneven sharing of electrons, so molecules are still neutral

negative: has larger share of electrons, excess of electrons
positive: lost some of its share of electrons

148
Q

dipole

A

separation of positive and negative charges

149
Q

polyatomic molecules polarity

A

symmetrical balanced dipoles= non-polar
methane: carbon is more electronegative but individual dipoles cancel each other out. results in a molecule with no overall dipole

in non-symmetrical molecules, individual dipoles don’t cancel each other, creating a net dipole making the molecule polar

150
Q

dipole dipole forces

A

only in polar molecules
results from attraction between positive and negative ends of polar molecules
weak since partial charge are small
more polar the molecule, the stronger the force

stronger force the higher the melting and boiling points because force bond molecules together in solid or liquid. higher energy is required to to break stronger bonds

151
Q

hydrogen bonding

A

only occurs in molecules in which a hydrogen atom is covalently bonded to a N,O or F
NOF are small and very electronegative so they strongly attract electrons in a covalent bond. creates a large partial positive charge on hydrogen atom, which is attracted to lone pairs of electrons in neighbouring NOF atoms

hydrogen in covalent bond with NOF is is exposed due to lack of electrons and is highly attracted to lone pairs of NOF in other molecules

strong intermolecular bond, x10 than dipole dipole, but 1/10 of ionic

152
Q

dispersion forces

A

forces of attraction in non polar substances (existence of intermolecular forces, without them nothing will hold molecules together and they would be gases)
caused by temporary (instantaneous) dipoles in molecules that result in random movement of the electrons surrounding molecule

strength increases as size of molecules increase. larger molecules have more electrons so it is easier to create temporary dipoles. larger molecules have higher melting and boiling points
molecules that form long chains have higher dispersion forces, more contact area to interact with it neighbouring molecules to form stronger forces

153
Q

how to increase polarity of a moelcule

A

larger difference in electronegativities

high degree of asymmetry in the shape of the molecule causing an imbalance in the bond dipole

154
Q

requirement of hydrogen bonding

A
  1. hydrogen atom covalent bonded to an NOF atom
  2. lone pair of electron of NOF atom of neighbouring molecules

H bonds are caused by NOF’s small radius and high electronegativities and single electron of hydrogen atom
larger radii reduce concentration of negative charge around them.

155
Q

hydrogen bonding in water

A

ice floats because it is less dense
in ice water molecules are held in a crystal lattice. in which molecules are held further part then in liquid water
when ice melts crystal lattice collapses and molecules pack together more tightly
crystal has greater volume, 4 hydrogen bonds to 4 neighbouring molecules

electrostatic attraction
strong in water because of large electronegativity difference meaning larger partial charge

156
Q

water properties

A
can dissolve many substances easily
high specific heat capacity 
high latent heat of vaporisation 
expands on freezing
react with CO2 to make glucose and oxygen
157
Q

water shape

A

lone pairs of water have greater repulsion than electron pairs in covalent bonds so they push the hydrogen atoms closer together

158
Q

going down hydrides (except water)

A

melting and boiling points increase
Intermolecular forces are stronger (dispersion)
dispersion forces increase with strength as mass increases

159
Q

water vs hydrides

A

hydrogen bonds in water give it a much higher boiling and melting point

160
Q

high surface tension of water

A

water molecules at the surface are not completely surrounded by other water molecules, so they form hydrogen bonds everywhere BUT above.

molecules in body of water have no net force but surface level molecules have a downwards force. water molecules at surface are so attracted to each other by strong hydrogen bonds

161
Q

surface tension meaning

A

measure of the resistance of a liquid to increasing its surface area

162
Q

heat capacity of water

A

measure of a substances capacity to absorb and store heat energy, how much energy a substance absorbs as temp increases

SHC: measure of how much energy is required to increase temp by 1º of 1 gram of substance

SHC of water is relatively high because of hydrogen binds. these bonds can absorbs and store large amount of heat energy before they break

163
Q

latent heat

A

when a something reaches its boiling/melting point the temp remains constant until all of substance changes state even though further energy is being absorbed

energy still being absorbed while state is changing is latent heat
energy absorbed by a fixed amount of substance as it changes state at its melting (fusion)/boiling (vaporisation)point
depends on strength of intermolecular forces

LHF of water is 6.0KJ/mol. energy required to disrupt ice lattice by breaking some hydrogen bonds
LHV of water is 44KJ/mol.

164
Q

dissolution

A

particles of solute separate
particles of solvent separate
particles of solute and solvent are attracted to each other

forces:
holding solute, holding solvent (H Bonds), form between solute and solvent

165
Q

like dissolves like

A

H bonds between water i such stronger that dispersion forces in non polar. attraction between water molecules cannot be overcome and water doesn’t separate to form a solution

166
Q

water dissolving covalent

A

molecular compounds that form H bonds:
strength of intermolecular forces are similar, so they readily interact with each other
the more polar, the more likely it will dissolve

molecular compounds that ionise:
highly polar molecular compounds form ions when dissolved in water
polar covalent bonds break producing ions, covalent bond forms between ion and water molecule (makes hydronium in HCl), ion dipole attraction between ions and water

167
Q

water dissolving ions

A

ion dipole: attraction between ion and polar molecule
if ion dipole attraction are strong enough, the water molecules can pull out ions from crystal lattice and into the solution

ionic compound–>hydrated ions (dissociation)
energy required to separate ions from lattice must be less than energy released when ions are hydrated

168
Q

solubility

A

maximum amount of solute that will dissolve in a given amount of solvent
increasing temp increases solubility, at higher temps solute and solvent have more energy to overcome forces of attraction that hold particles together in the solid

saturated: no more solute can be dissolved at a certain temp
unsaturated: contains less solute needed to make solution saturated
supersaturated: contains more dissolved solute than a saturated solution

169
Q

crystallisation

A

when an unsaturated solution becomes saturated and crystals form.
1. cooling: may reduce the solubility of a dissolved solute to the point where not all of the substance available is soluble. slow cooling = larger crystals
2. evaporating the solvent from the solution
falser rate of evaporation = smaller crystals

170
Q

gases in water

A

Solubility decreases with rising temp

deoxygenates water so water must be cooled before released into environment

171
Q

chromatography

A

technique used to separate and analyse the substances present in a mixture. it can be used to analyse numerous organic and inorganic substances.
eg: contaminants in water, toxic gases in air, additives and impurities in food, drugs in blood
chromatography only works for small amounts of different substances because the solvent can only carry small amount of the mixture with it.

172
Q

how chromatography works

A

has stationary phase (solid/liquid), and a mobile phase (liquid/gas). mobile phase moves up stationary phase due to capillary action.

as components of the mixture are swept upwards over the stationary phase by the solvent, they undergo a continual process of adsorption onto the solid stationary phase, followed by desorption and dissolving into the mobile phase. the ability of component molecules to adsorb depend on the polarity of stationary phase and molecules. attraction between component and solvent molecules depend on the polarity as well.

173
Q

components in chromatography

A

chemicals in a mixture

174
Q

chromatogram

A

output of a chromatography procedure
in TLC and paper: patterns of bands or spots formed on a plate or on the paper
in HPLC: graph produced

175
Q

rate of movement in chromatography depends on

A

how strongly the component adsorbs onto the stationary phase

how readily the component dissolves in the mobile phase

176
Q

paper and TLC

A

qualitative analysis
paper: the stationary phase is high quality absorbent paper
TLC: the stationary phase is a thin layer of a fine powder (aluminium oxide) spread on a glass or plastic plate

small spot of solution of sample is placed on one end of chromatography paper/plate, spot is called the origin. the paper/plate is placed in a container with the solvent. origin is a bit above the solvent level, so that components can be transported up the paper/plate and not be dissolved in the solvent.

as the solvent rises up the paper/plate, the component of each sample separate depending on their attraction tot the stationary phase and their solubility in the solvent

177
Q

Identifying components of a mixture

chromatography

A
  1. include standards of known chemicals on the same chromatogram as the unknown sample and comparing the resulting positions of the unknown components with those of the known samples
  2. calculate the retardation factor of the sample and comparing these with the values of known samples
    RF= distance component travelled/ distance solvent travelled
    *from the origin

component most strongly adsorbed to the stationary phase moves the shortest distance and has lower RF value

178
Q

solvent front

A

describe the movement of the solvent during chromatography. it is visible as the wet moving edge of the solvent as the solvent travels up the stationary phase

179
Q

retardation factor

A

each component has a characteristic RF value for the conditions under which the chromatogram was obtained
thing that change RF value:
changes in temp
type of stationary phase
amount of solvent vapour around paper/plate
type of solvent

180
Q

colourless compounds

A

many organic compounds fluoresce and appear blue when viewed under UV light
chromatogram can be sprayed with a chemical that reacts to form coloured/fluorescent compounds

181
Q

paper v TLC

A
paper:
cheap
little preparation 
more efficient for polar and water soluble compounds
easy to handle and store

TLC:
detects smaller amounts
better separation for less polar compounds
corrosive materials can be used
wide range of stationary phases can be used

only use a give a guide to identify the chemical, since for. a particular combination of stationary phase and mobile phase, many different chemicals may have similar RF values.

182
Q

column chromatography

A

the solid stationary phase is packed into a glass column. the sample is applied carefully to the top of the packed column, and a solvent which acts as a mobile phase is dripping slowly onto the column from a reservoir above
a tap at the bottom of the column allows the solvent (eluent) to leave the column at the same rate it enters at the other end

183
Q

paper and TLC summary

A

components undergo a continual process of adsorption to stationary phase and desorption back into mobile phase
components undergo adsorption and desorption to different degrees depending on the strength of their attraction to the stationary and mobile phases. thus components separate as they move past the stationary phase

184
Q

HPLC

A

based on column chromatography
allows sensitive analysis of a wide range of mixtures
separation and identification of complex mixtures of similar compounds (contaminants soluble in water, drugs in blood, hydrocarbons in oil samples, presence and concentration of dioxins; insecticide, pesticides and oil spills in water)

particles in the solid used in HPLC column are 10-20 times more smaller than column chromatography, allows more frequents adsorption and desorption of components giving better separation
small particle size in HPLC creates a considerable resistance to flow of mobile phase, so solvent is pumped through column in high pressure

range of solids can be used in HPLC, some with chemicals specially bonded to their surfaces to improve the separation of particular classes of compounds

components are detected by passing the eluent stream through Uv light beam. many organic components absorb UV light, so when an organic compound passes in front of the beam of light, a reduced signal is picked by a detector. amount of light received by detector is recorded on a chart that moves slowly at a constant speed or sent to a computer. resulting trace Is called a chromatogram. each component forms one peak in the chromatogram.

can separate compounds with relative molecular mass 1000 or even more

185
Q

gas chromatography

A

most sensitive technique
limited to components that can be readily vaporised without decomposing (relative molecular mass <300)

analysis of trace contaminants, or tiny amounts of very potent components (drugs in urine)

mobile phase is an inert gas (nitrogen), as a carrier gas
small amount of sample is injected into the top of the column through an injection port. the port is heated to vaporise the sample which is swept into the column by the carrier gas
the column is a series of loops of glass/metal (length=2-3m, diameter=4mm), it is heated. the column is packed with a porous solid coated with an ester/liquid hydrocarbon with a high BP; or packed with and absorbent solid such as silica gel/ alumina. this is the stationary phase

components repeatedly interact with the stationary phase and are swept forward by the carrier gas. components that adsorb least strongly to the stationary phase are swept out first by the gas. as components emerge from the end of the column, they are sensed by the detector.

186
Q

application of GC and HPLC

A

qualitative: what chemical is present in the sample
quantitative: how much of each chemical is present

qualitative: how much and purity of component
a solution of a pure compound that is thought to be one of the components is injected into column under same conditions. chromatogram is compared.
the same compound will have the same retentions time if conditions are kept the same
can also be identified by adding known compound to sample (spiking), creates a much bigger peak in the chromatogram

Quantitative: to determine concentration of a component, its peak are air compared with peak areas of samples of the same chemical at known concentrations
standard solution: has an accurately known concentration
calibration curve (peak area against concentration) determines unknown concentration

187
Q

retention time

A

time taken for component to pass through column

characteristic of the component for the conditions of the experiment.

188
Q

carbon

A

forms more compounds than all elements combined

  • 4 valence electrons, 4 needed
  • strong covalent bonds with other carbons
  • bonds can be single, double or triple
189
Q

crude oil

A

when dead animals, plants and micro-organisms were buried by sand, the organisms accumulate as sediment and gradually become part of earth’s crust

increase in temp and pressure make oil and fat into hydrocarbons
crude oil is a mixture of hydrocarbons. it has a low density so it migrates up but I slacked by impervious rock
accumulation of oil and gas creates oil field

refining: not used in raw state, fractional distillation. crude oil separated to components made of range of hydrocarbons with similar BP
heavier components (fractions)-> cracking
breaks larger hydrocarbons molecules results in two smaller molecules one of which has a carbon-carbon double bond
190
Q

alkane

A

hydrocarbon = only carbon and hydrogen

hydrocarbon with only single bond
it is saturated: only carbon-carbon single bonds

weak forces, non polar (increase in size increase dispersion force and MP+BP)
CnH2n+2

structural isomers same formula different arrangement
akyl group: CnH2n+1

methyl propane: methyl must be on second carbon

191
Q

homologous series

A

series of compounds with similar properties and same general formula
where each member has one CH2 unit than the previous member
- similar structure
- pattern to physical properties (BP)
- similar chemical properties
- same general formula

192
Q

alkenes

A
double bond (2 pairs of electrons shared)
unsaturated: one more double/triple bonds

alkene: homolog series of hydrocarbons with a carbon-carbon double bond
CnH2n, more reactive, non polar (not soluble in water)

geometric isomers: same order, different arrangement. atoms in double bond are fixed unlike single bonds

193
Q

benzene

A

C6H6
stable has a ring structure
aromatic hydrocarbon
electrons that make up double bonds aren’t in fixed positions and can move through ring
carbon-carbon bond are same length, molecule is more stable than expected of unsaturated molecule

bonds between carbon are intermediate between single and double bonds

194
Q

substitution reaction

A

alkane and halogen (with UV light)
carbon-hydrogen bond broken replaced with carbon-halogen bond

benzene and halogen (with catalyst AlCl3 or AlBr3)

halogen can be in excess or limited

195
Q

addition reaction

A

addition of small molecule to double bond of alkene

  • 2 reactant to 1 product
  • carbon-carbon double bond to a single bond
  • unsaturated to saturated
  • small molecule added across double bond, forms bond on each end of double bond
196
Q

alkene + H2O

A

makes an alcohol
hydration reaction because water is a reactant

ethene + H2O -> ethanol

uses catalyst
at 300ºC, gaseous reactants, solid catalyst, gaseous products (easy to separate catalyst and product)

197
Q

alkene + hydrogen gas

A

in presence of metal catalyst (Ni)
forms alkanes and saturated
hydrogenation

etene + H2 -> ethane

too slow to proceed at room temp without a catalyst

198
Q

alkene + halogen

A

halogen adds across the double bond
ethene and bromine -> 1,2-dibromoethane

proceeds at room temp without a catlyst

199
Q

alkene + hydrogen halide

A

HCL, Her, HF, HI

adds across double bond

  • asymmterical alkene + asymmetrical reactant -> isomers made
200
Q

unsaturation test

A

bromine water to determine if substance has double bonds (unsaturated)

  • aqueous Br2 solution added to alkane has no reaction and no ocular change
  • Br2 and alkene has an addition reaction and orange colour disappears

substitution reaction is much slower than this addition reaction at room temp without catalyst
addition reaction has an instant change

201
Q

hydrocarbons and combustion

A

can be incomplete or complete

202
Q

precipitation reaction

A

occurs if ions in solution combine to form a new compound that is insoluble in water
compound=precipitate

when one solution is added to another mixture formed will contain all of the ions. ions move independently and as they move, they collide with one another. if cations and anions collide they can join together to form a precipitate
hydrated ions -> attraction between ions -> ionic lattice

203
Q

concentration

A

describes relative amount of solute and solvent present in the solution.

grams/L

ppm: mg/kg

M: mol/L

*solute/solution

204
Q

dilution

A

adding more solvent to a solution, decreases concentration

C1V1=C2V2

205
Q

soluble base

A

alkali

206
Q

properties of acids

A
turns litmus indicator red
corrosive
taste sour
react with bases
ph less than 7
conduct electric current
207
Q

properties of bases

A
turns litmus blue
caustic and feel slippery
bitter taste 
react with acids
ph greater than 7
solutions conduct an electric current
208
Q

acid

A

substance capable of making hydrogen ions in solution, or donating a hydrogen ion

209
Q

base

A

substance capable of producing hydroxide ions in solution or accepting a proton (hydrogen ion)

210
Q

Arrhenius model of acid

A

acid is defined as a substance that is ionised in water to produce hydrogen ions
ionisation: removal of one or more electrons from an atom or ion. reaction of a molecular substance with a solvent to form ions in solution

211
Q

polyprotic acid

A

acids that react to form more than one hydrogen ion per molecule. molecules have more than one proton that can be ionised.
in general hydrogen atoms that are bonded to a highly electronegative atom (polar bonds are ionised in solution)

212
Q

diprotic acid

triprotic acid

A

donates two hydrogen ions when ionised

donates three protons when ionised

213
Q

hydronium ion

A

single proton can’t exist in water, H ion attracted to lone pair of electrons on a water molecule
(H3O+)

214
Q

Arrhenius model of bases

A

substance that dissociates in water to form hydroxide ions. presence of hydroxide account for common properties of bases

215
Q

acids and bases as electrolytes

A

conduct electricity because of free moving ions with charges
HCl: ionises in water to form H and CL ions

216
Q

neutralisation

A

according to Arrhenius model: when acids and bases react the hydrogen and hydroxide ions combine to form water

adjustment of acidity
if a solution of metal hydroxide and acid is added together, hydroxide ions react with the hydrogen ions.. once all hydroxide ions have reacted with hydrogen ions (forming water) that is when acid and base have neutralised

217
Q

limitations of Arrhenius model

A

doesn’t explain why some substances without hydrogen can form acidic solutions when mixed with water
co2 and sos make acidic solutions
nh3 and NaHCO3 mixed with water make basic solutions

this is explained by bronsted Lowry theory: acid donates hydrogen ion, and bases accepts this ion

218
Q

strong and weak acids

A

strong (acids that ionise readily, complete ionisation, solutions contain ions with virtually no unreacted acid molecules remaining)
HCl, H2SO4, HNO3

weak (partial ionisation, only small amount of acid molecules ionise)
acetic acid

219
Q

strong and weak bases

A

strong (completely dissociate)
Group 1+2 oxides and hydroxides

weak (only small proportion ionised at any instant)
ammonia, metal (phosphates, carbonated and hydrogen carbonate )

220
Q

strength vs concentration

A

concentration: how much substance is dissolve in solution
strength: to what degree acid is ionised or base is dissociated

221
Q

pH

A

range of hydrogen ion concentration on a scale to measure acidity
pH decreases as H+ ions increase

222
Q

acid and metal carbonate

A

lime water test: confirms presence of CO2 gas, saturated solution of calcium hydroxide. when Coz is bubbled through the solution, it will turn milky/cloudy due to precipitation of CaCO3

Ca(OH)2 + CO2 -> CaCO3 + H2O