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AQA A-Level Chemistry

A-Level · AQAChemistry57 Notizen in 17 Ordnern, 313 KB

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Notes for AQA A-Level Chemistry (7405), in folders for the specification's physical, inorganic and organic chemistry in its order, with a note for each sub-topic or pair of sub-topics. The twelve required practicals have a folder of their own, as the method and the science behind it. Delete any note your course leaves out once the notes are yours.

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Was enthalten ist

  • Physical chemistry
    • Atomic structure
      • Atomic structure and mass spectrometry6 KB
      • Electron configuration and ionisation energy6 KB
    • Amount of substance
      • Moles, concentration and gases4 KB
      • Formulae, equations, yield and atom economy6 KB
    • Bonding
      • Ionic, covalent and metallic bonding, and structures7 KB
      • Shapes of molecules and ions5 KB
      • Bond polarity and intermolecular forces6 KB
    • Energetics
      • Enthalpy changes, calorimetry, Hess's law and bond enthalpies7 KB
      • Born-Haber cycles and lattice enthalpy6 KB
      • Entropy and free-energy change5 KB
    • Kinetics
      • Collision theory, Maxwell-Boltzmann distribution and catalysts4 KB
      • Rate equations and orders of reaction6 KB
      • The Arrhenius equation3 KB
    • Equilibria
      • Dynamic equilibrium, Le Chatelier's principle and Kc7 KB
      • The equilibrium constant Kp3 KB
    • Redox and electrochemistry
      • Oxidation states and redox equations5 KB
      • Electrode potentials and electrochemical cells7 KB
      • Batteries and fuel cells5 KB
    • Acids and bases
      • Acids, bases, pH and Kw5 KB
      • Weak acids and Ka4 KB
      • Titration curves and indicators5 KB
      • Buffer solutions5 KB
  • Inorganic chemistry
    • Periodicity and the Period 3 elements4 KB
    • Period 3 oxides5 KB
    • Group 2, the alkaline earth metals4 KB
    • Group 7, the halogens5 KB
    • Halide tests, chlorine and chlorate(I)4 KB
    • Transition metals: properties, ligands and complex ions7 KB
    • Shapes and isomerism of complex ions3 KB
    • Colour, oxidation states and redox titrations of transition metals8 KB
    • Catalysis by transition metals5 KB
    • Reactions of metal ions in aqueous solution5 KB
  • Organic chemistry
    • Foundations
      • Nomenclature, formulae and reaction mechanisms7 KB
      • Isomerism6 KB
    • Hydrocarbons and halogenoalkanes
      • Alkanes: crude oil, cracking and combustion6 KB
      • Free-radical substitution and ozone depletion4 KB
      • Halogenoalkanes: nucleophilic substitution and elimination6 KB
      • Alkenes: electrophilic addition5 KB
    • Oxygen-containing compounds
      • Alcohols7 KB
      • Aldehydes and ketones5 KB
      • Carboxylic acids and esters5 KB
      • Acyl chlorides, acid anhydrides and amides5 KB
    • Aromatics, nitrogen compounds and polymers
      • Benzene and electrophilic substitution6 KB
      • Amines5 KB
      • Polymers: addition and condensation7 KB
      • Amino acids and proteins6 KB
      • Enzymes, DNA and anticancer drugs5 KB
    • Analysis and synthesis
      • Test-tube tests, mass spectrometry and infrared spectroscopy6 KB
      • Nuclear magnetic resonance spectroscopy6 KB
      • Chromatography5 KB
      • Organic synthesis5 KB
  • Required practicals
    • Volumetric solutions and titrations7 KB
    • Measuring enthalpy changes and cell EMF6 KB
    • Measuring reaction rates6 KB
    • Identifying cations and anions6 KB
    • Distillation and preparing pure organic compounds7 KB
    • Tests for organic functional groups and thin-layer chromatography5 KB

Die erste Notiz

Physical chemistry / Atomic structure / Atomic structure and mass spectrometry

Particles in the atom

An atom has a small, dense nucleus made of protons and neutrons, with electrons in the space around it. The model has changed over time: Dalton pictured solid indivisible spheres, Thomson found electrons and described a positive sphere with electrons embedded in it, Rutherford's scattering experiment showed that the positive charge and nearly all the mass sit in a tiny nucleus, and Bohr and later quantum models placed the electrons in shells and orbitals of fixed energy.

ParticleRelative chargeRelative mass
Proton+11
Neutron01
Electron-111840\frac{1}{1840} (about 0.0005)

The atomic (proton) number, ZZ, is the number of protons in the nucleus and fixes which element it is. The mass number, AA, is the number of protons plus neutrons. An atom is neutral, so it has as many electrons as protons; an ion has gained or lost electrons.

Counting particles

For an ion of element X with mass number AA, atomic number ZZ and charge nn:

  • protons =Z= Z
  • neutrons =A−Z= A - Z
  • electrons =Z−n= Z - n for a positive ion of charge n+n+, and Z+nZ + n for a negative ion of charge n−n-

For X27X2227AlX3+\ce{^{27}Al^{3+}} (atomic number 13) there are 13 protons, 14 neutrons and 13−3=1013 - 3 = 10 electrons. For X32X2232SX2−\ce{^{32}S^{2-}} (atomic number 16) there are 16 protons, 16 neutrons and 18 electrons.

Isotopes

Isotopes are atoms of the same element with the same number of protons but different numbers of neutrons, so they have different mass numbers. Their chemical properties are the same, because chemical behaviour is governed by the electrons and so by the proton number. Physical properties that depend on mass, such as density and the rate of diffusion, differ slightly.

Chlorine has two common isotopes, X35X2235Cl\ce{^{35}Cl} (18 neutrons) and X37X2237Cl\ce{^{37}Cl} (20 neutrons). Both have 17 protons and 17 electrons in the neutral atom.

Relative masses

The relative isotopic mass is the mass of an atom of an isotope compared with one twelfth of the mass of an atom of carbon-12. The relative atomic mass, ArA_r, is the weighted mean mass of an atom of an element compared with one twelfth of the mass of an atom of carbon-12, where the mean is taken over the naturally occurring isotopes. The relative molecular mass, MrM_r, is the mean mass of a molecule compared with one twelfth of the mass of an atom of carbon-12. For ionic compounds the term relative formula mass is used, because there are no separate molecules. All three are ratios, so they have no units.

Relative atomic mass from isotopic abundance
Ar=∑(isotopic mass×abundance)∑abundance A_r = \frac{\sum (\text{isotopic mass} \times \text{abundance})}{\sum \text{abundance}}

The abundances can be percentages or relative intensities from a mass spectrum, because the denominator divides out the total.

A sample of magnesium contains 78.6% X24X2224Mg\ce{^{24}Mg}, 10.1% X25X2225Mg\ce{^{25}Mg} and 11.3% X26X2226Mg\ce{^{26}Mg}.

Ar=(24×78.6)+(25×10.1)+(26×11.3)100=1886.4+252.5+293.8100=24.327≈24.3 \begin{aligned} A_r &= \frac{(24 \times 78.6) + (25 \times 10.1) + (26 \times 11.3)}{100} \\ &= \frac{1886.4 + 252.5 + 293.8}{100} \\ &= 24.327 \approx 24.3 \end{aligned}

The answer is given to three significant figures, matching the data. It lies close to 24 because the lightest isotope is by far the most abundant.

A common exercise runs the other way. Boron has two isotopes, X10X2210B\ce{^{10}B} and X11X2211B\ce{^{11}B}, and Ar=10.81A_r = 10.81. If the abundance of X10X2210B\ce{^{10}B} is xx per cent then

10x+11(100−x)=10811100−x=1081x=19 \begin{aligned} 10x + 11(100 - x) &= 1081 \\ 1100 - x &= 1081 \\ x &= 19 \end{aligned}

so boron is 19% X10X2210B\ce{^{10}B} and 81% X11X2211B\ce{^{11}B}.

Time of flight mass spectrometry

A mass spectrometer measures the mass-to-charge ratio, m/zm/z, of ions and the relative amount of each. In a time of flight (TOF) instrument the stages are:

  1. Ionisation: The sample is vaporised and ionised, either by electron impact (a beam of high-energy electrons knocks an electron off each atom or molecule, giving XX+\ce{X+}) or by electrospray (the sample is dissolved and sprayed through a needle at high voltage, so each molecule picks up a proton and becomes XHX+\ce{XH+}).
  2. Acceleration: The positive ions are accelerated by an electric field so that every ion has the same kinetic energy.
  3. Ion drift: The ions pass through a flight tube with no field. Because the kinetic energy 12mv2\frac{1}{2}mv^2 is the same for all ions, lighter ions travel faster and reach the detector sooner.
  4. Detection: The ions hit a detector, which records the time of arrival and produces a current proportional to the number of ions arriving.
  5. Data analysis: A computer converts the flight times into m/zm/z values and plots a mass spectrum, in which the height of each peak shows the relative abundance of that ion.

The flight time tt over a distance dd comes from v=d/tv = d/t and KE=12mv2\text{KE} = \frac{1}{2}mv^2, giving t2=md22 KEt^2 = \frac{m d^2}{2\,\text{KE}}, so tt increases with the square root of the mass. The instrument must be under a vacuum so that the ions do not collide with air molecules.

Reading a spectrum

For an element, each peak is an isotope with a charge of 1+, so the m/zm/z value is the relative isotopic mass and the peak height gives the abundance. The spectrum of an element can therefore be used to work out its ArA_r with the weighted mean above, and the pattern of peaks helps to identify the element.

Chlorine gas, ClX2\ce{Cl2}, gives more peaks than the atoms alone. The molecular ions are X35X2235Cl−X35X2235ClX+\ce{^{35}Cl-^{35}Cl+} at 70, X35X2235Cl−X37X2237ClX+\ce{^{35}Cl-^{37}Cl+} at 72 and X37X2237Cl−X37X2237ClX+\ce{^{37}Cl-^{37}Cl+} at 74, alongside atomic ions at 35 and 37.

For a compound, the peak at the highest m/zm/z is the molecular ion peak, and its m/zm/z equals the relative molecular mass MrM_r of the compound. Fragmentation peaks at lower values are dealt with in the note on organic analysis.

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