Unit 1: Structure, Bonding and Introduction to Organic Chemistry AS

Syllabus
2017
Section
—
Level
AS

Topic 1: Formulae, Equations and Amount of Substance

Syllabus
2017
Topic
—
Level
AS

Atoms, ions and formulae describe different levels of matter

Chemists use each term for a different kind of particle, substance or formula. Keeping those levels separate prevents errors when interpreting equations and composition data.

Term Precise meaning Example
atom Smallest particle of an element that retains that element's identity Ne\ce{Ne}
element Substance containing atoms with the same proton number copper
ion Atom or group with a net charge after electron loss or gain SOX4X2−\ce{SO4^{2-}}
molecule Discrete group of atoms joined by covalent bonds OX2\ce{O2} or HX2O\ce{H2O}
compound Two or more elements chemically combined in fixed proportions NaCl\ce{NaCl} or HX2O\ce{H2O}

An empirical formula gives the simplest whole-number ratio of atoms, whereas a molecular formula gives the actual number of each type of atom in one molecule. For example, glucose has empirical formula CHX2O\ce{CH2O} and molecular formula CX6HX12OX6\ce{C6H12O6}.

A molecule may be an element, such as OX2\ce{O2}, so 'molecule' does not mean 'compound'. Ionic and giant substances have formula units rather than discrete molecules.

The mole counts chemical entities on a laboratory scale

Amount of substance is measured in moles. One mole contains the Avogadro constant, L=6.02×1023 mol−1L=6.02\times10^{23}\,\mathrm{mol^{-1}}, of the specified entities: atoms, molecules, ions or formula units.

N=nL\qquad n=\frac{N}{L}

For 0.250 mol0.250\,\mathrm{mol} of sodium chloride, the number of formula units is 0.250×6.02×1023=1.51×10230.250\times6.02\times10^{23}=1.51\times10^{23}. It also contains that many NaX+\ce{Na+} ions and that many ClX−\ce{Cl-} ions, so the total number of ions is twice the number of formula units.

Always name the entity being counted. Multiplying by the number of atoms or ions per entity is a separate step; one mole of COX2\ce{CO2} molecules contains three moles of atoms in total.

Balanced equations conserve atoms and charge

A full equation shows all reactants and products; an ionic equation keeps only the species that undergo chemical change. Both must conserve every element and the total charge, and every species needs the correct state symbol.

  1. Write correct chemical formulae; never change subscripts to balance an equation.
  2. Adjust coefficients until each element is conserved.
  3. Add (s)(s), (l)(l), (g)(g) and (aq)(aq) from the physical states.
  4. For an ionic equation, split soluble aqueous ionic substances into ions.
  5. Cancel spectator ions that appear unchanged on both sides, then check atoms and charge.

\ce{AgNO3(aq) + NaCl(aq) -> AgCl(s) + NaNO3(aq)}\ce{Ag+(aq) + Cl-(aq) -> AgCl(s)}

Do not split solids, liquids, gases or weakly ionised substances into aqueous ions. State symbols carry chemical meaning: AgCl(aq)\ce{AgCl(aq)} would contradict the observed precipitate.

Relative mass, molar mass and ppm answer different questions

Relative masses compare particles with one twelfth of the mass of a carbon-12 atom. They are ratios and therefore have no unit. Molar mass is the mass of one mole and is measured in g mol−1\mathrm{g\,mol^{-1}}.

Quantity Meaning and use
ArA_r relative atomic mass; isotopic average for an element on the 12C^{12}\ce{C} scale
MrM_r sum of ArA_r values for a discrete molecule
relative formula mass corresponding sum for an ionic or giant structure, which has no discrete molecule
molar mass, MM mass per mole; numerically equal to the appropriate relative mass in g mol−1\mathrm{g\,mol^{-1}}

For MgClX2\ce{MgCl2}, the relative formula mass is 24.3+2(35.5)=95.324.3+2(35.5)=95.3, so its molar mass is 95.3 g mol−195.3\,\mathrm{g\,mol^{-1}}. Calling this an MrM_r suggests discrete molecules and is inappropriate for the giant ionic lattice.

\mathrm{ppm}=\frac{\text{amount of component}}{\text{total amount}}\times10^6

Use matching quantities in the fraction. For atmospheric gases, ppm commonly expresses a mole or volume fraction: 420420 ppm means 420420 parts of that gas per million parts of air, not 420%420\%.

Solution concentration links amount or mass to total volume

Concentration states how much solute is present per unit volume of solution. Use the final solution volume, not the volume of solvent added, and convert cm3\mathrm{cm^3} to dm3\mathrm{dm^3} before using these relationships.

c=\frac{n}{V}\quad(\mathrm{mol,dm^{-3}})\qquad c_m=\frac{m}{V}\quad(\mathrm{g,dm^{-3}})\qquad c_m=cM

Dissolving 5.85 g5.85\,\mathrm{g} of NaCl\ce{NaCl} and making the solution up to 500 cm3500\,\mathrm{cm^3} gives V=0.500 dm3V=0.500\,\mathrm{dm^3}. With M(NaCl)=58.5 g mol−1M(\ce{NaCl})=58.5\,\mathrm{g\,mol^{-1}}, n=0.100 moln=0.100\,\mathrm{mol}, so c=0.200 mol dm−3c=0.200\,\mathrm{mol\,dm^{-3}}. The mass concentration is 5.85/0.500=11.7 g dm−35.85/0.500=11.7\,\mathrm{g\,dm^{-3}}.

The numerical values in mol dm−3\mathrm{mol\,dm^{-3}} and g dm−3\mathrm{g\,dm^{-3}} are not interchangeable; molar mass provides the conversion. Titration calculations are outside this Topic 1 objective.

Composition data reveal empirical and molecular formulae

An empirical formula comes from a mole ratio, not directly from a mass ratio. Convert every measured mass or percentage into moles before finding the simplest whole-number ratio.

  1. Treat percentages as masses in a 100 g100\,\mathrm{g} sample, or use the measured masses directly.
  2. Divide each mass by the element's ArA_r to obtain moles.
  3. Divide all mole values by the smallest.
  4. If necessary, multiply the whole ratio to remove values such as 1.51.5 or 1.331.33.
  5. Write the empirical formula. For a molecular formula, calculate k=Mr/(empirical-formula mass)k=M_r/(\text{empirical-formula mass}) and multiply every subscript by the integer kk.

A compound containing 40.0%40.0\% C, 6.7%6.7\% H and 53.3%53.3\% O gives mole values 40.0/12.040.0/12.0, 6.7/1.06.7/1.0 and 53.3/16.053.3/16.0, a ratio close to 1:2:11:2:1. Its empirical formula is CHX2O\ce{CH2O}. If Mr=180M_r=180, then k=180/30=6k=180/30=6 and the molecular formula is CX6HX12OX6\ce{C6H12O6}.

Round only after identifying a defensible near-integer ratio. Arbitrarily rounding 1.51.5 to 22 changes the composition; multiply the entire ratio instead.

Reacting-mass calculations follow the equation's mole ratio

A balanced equation relates amounts in moles. Convert the known mass to moles, apply the stoichiometric coefficient ratio, then convert the required amount back to mass.

n=\frac{m}{M}\quad\longrightarrow\quad\text{mole ratio}\quad\longrightarrow\quad m=nM

\ce{Mg + 2HCl -> MgCl2 + H2}

For 4.80 g4.80\,\mathrm{g} Mg, n(Mg)=4.80/24.3=0.198 moln(\ce{Mg})=4.80/24.3=0.198\,\mathrm{mol}. The 1:11:1 coefficient ratio gives 0.198 mol0.198\,\mathrm{mol} MgClX2\ce{MgCl2}. With M(MgClX2)=95.3 g mol−1M(\ce{MgCl2})=95.3\,\mathrm{g\,mol^{-1}}, the theoretical mass is 18.8 g18.8\,\mathrm{g}.

Coefficients compare moles, not masses. If more than one reactant amount is supplied, identify the limiting reactant before calculating product; an excess reactant cannot determine the product amount.

Gas amounts connect equation ratios, molar volume and $pV=nRT$

Convert a gas volume to moles, use the balanced equation's mole ratio, and convert to the requested quantity. The conversion method depends on the stated temperature and pressure.

n=\frac{V}{V_m}\qquad pV=nRT

At room temperature and pressure, use the stated or accepted molar volume (commonly 24.0 dm3 mol−124.0\,\mathrm{dm^3\,mol^{-1}}). For other conditions, use pV=nRTpV=nRT: pressure in Pa, volume in m3\mathrm{m^3}, temperature in K and R=8.31 J K−1 mol−1R=8.31\,\mathrm{J\,K^{-1}\,mol^{-1}}. The same equation can find the molar mass of a volatile liquid from the mass and amount of its vapour.

2.40 dm32.40\,\mathrm{dm^3} of gas at room conditions is 2.40/24.0=0.100 mol2.40/24.0=0.100\,\mathrm{mol}. Under specified non-room conditions, 120 cm3=1.20×10−4 m3120\,\mathrm{cm^3}=1.20\times10^{-4}\,\mathrm{m^3} and 25∘C=298 K25^\circ\mathrm{C}=298\,\mathrm{K} before substitution into n=pV/(RT)n=pV/(RT).

A gas-volume ratio equals the equation's mole ratio only when the gases are compared at the same temperature and pressure. Never insert dm3\mathrm{dm^3}, kPa\mathrm{kPa} or degrees Celsius into pV=nRTpV=nRT with the stated SI value of RR.

Yield measures recovery; atom economy measures reaction design

Percentage yield compares the product actually obtained with the theoretical amount. Percentage atom economy asks what fraction of the products' mass is in the desired product, using the balanced equation.

%,\text{yield}=\frac{\text{actual yield}}{\text{theoretical yield}}\times100%,\text{atom economy}=\frac{\text{stoichiometric mass of desired product}}{\text{sum of stoichiometric masses of all products}}\times100

For CaCOX3→CaO+COX2\ce{CaCO3 -> CaO + CO2}, if CaO\ce{CaO} is desired, the atom economy is 56.1/(56.1+44.0)×100=56.0%56.1/(56.1+44.0)\times100=56.0\%. If the theoretical yield of CaO\ce{CaO} is 5.00 g5.00\,\mathrm{g} but 4.20 g4.20\,\mathrm{g} is isolated, the percentage yield is 84.0%84.0\%.

Yield can fall because reaction is incomplete, side reactions occur, or product is lost during separation. Atom economy is fixed by the chosen balanced reaction and desired product; it does not improve merely because technique or catalyst improves yield.

A high yield and a high atom economy are different advantages. Include stoichiometric coefficients when more than one mole of a product appears in the equation.

Experimental mole ratios test a formula or equation

To determine a formula, measure the amounts of elements that combine and convert them to a simplest whole-number mole ratio. To confirm an equation, compare a measured mass change or gas amount with the ratio predicted by a balanced candidate equation.

  1. Record masses or volumes with suitable precision and identify which measured change belongs to each substance.
  2. Repeat heating or reaction to constant mass where appropriate.
  3. Convert each quantity to moles using molar mass or gas conditions.
  4. Divide by the smallest amount and test whether the ratio is close to small whole numbers.
  5. Compare the experimental ratio with the proposed formula or equation, then state whether the data support it.

Evaluate direction as well as size of error. Incomplete reaction can leave too little mass change; loss of solid can make mass loss too large; oxidation by air can add mass; gas leaks or dissolution can reduce the collected volume. Repeats expose random variation, but repeating does not remove a systematic leak or calibration error.

A non-integer raw ratio is not automatically evidence for an unusual formula. First consider uncertainty, incomplete reaction, contamination and whether every product was measured.

Core Practical 1: measure the molar volume of a gas

React a known amount of a solid with an excess reagent, collect the gas and divide its volume by the moles formed. A typical route reacts a measured mass of magnesium with excess dilute acid and collects hydrogen in a gas syringe or calibrated inverted vessel.

  1. Measure the magnesium mass and calculate n(Mg)n(\ce{Mg}).
  2. Place excess dilute acid in a sealed reaction vessel connected to the gas collector.
  3. Add the magnesium, seal immediately and allow the reaction to finish.
  4. Record gas volume, room temperature and pressure; use Mg+2 HX+→MgX2++HX2\ce{Mg + 2H+ -> Mg^{2+} + H2} to obtain n(HX2)n(\ce{H2}).
  5. Convert the volume to dm3\mathrm{dm^3} and calculate Vm=V/nV_m=V/n in dm3 mol−1\mathrm{dm^3\,mol^{-1}}. Repeat and compare values.

V_m=\frac{V(\text{gas})}{n(\text{gas})}

Check all joints for leaks, fit the bung before appreciable gas escapes, keep the gas-collection capacity above the predicted volume, and read the scale at eye level. Gas loss makes VmV_m too low; using too much solid may exceed the apparatus range. Wear eye protection with acid and keep hydrogen away from flames.

Observations connect full equations to ionic change

An observation is macroscopic evidence of a chemical change. A full equation identifies the substances used; the ionic equation identifies the particles responsible for the visible change. State symbols link the two levels.

Reaction and observation Full equation Net ionic change
displacement: zinc gains a reddish-brown copper coating and the blue solution fades Zn(s)+CuSOX4(aq)→ZnSOX4(aq)+Cu(s)\ce{Zn(s) + CuSO4(aq) -> ZnSO4(aq) + Cu(s)} Zn(s)+CuX2+(aq)→ZnX2+(aq)+Cu(s)\ce{Zn(s) + Cu^{2+}(aq) -> Zn^{2+}(aq) + Cu(s)}
acid + metal: magnesium dissolves and a colourless gas effervesces Mg(s)+2 HCl(aq)→MgClX2(aq)+HX2(g)\ce{Mg(s) + 2HCl(aq) -> MgCl2(aq) + H2(g)} Mg(s)+2 HX+(aq)→MgX2+(aq)+HX2(g)\ce{Mg(s) + 2H+(aq) -> Mg^{2+}(aq) + H2(g)}
precipitation: mixing the solutions forms a white solid AgNOX3(aq)+NaCl(aq)→AgCl(s)+NaNOX3(aq)\ce{AgNO3(aq) + NaCl(aq) -> AgCl(s) + NaNO3(aq)} AgX+(aq)+ClX−(aq)→AgCl(s)\ce{Ag+(aq) + Cl-(aq) -> AgCl(s)}

For displacement, electron transfer changes the metal and ion identities. In the acid reaction, HX+\ce{H+} becomes hydrogen gas. In precipitation, two aqueous ions form an insoluble lattice. Spectator ions remain aqueous and cancel from the ionic equation.

Write what is actually seen—colour change, bubbles, solid formation or disappearance—not an inference such as 'ions reacted'. A correct ionic equation must still balance atoms and charge and include state symbols.

Topic 2: Atomic Structure and the Periodic Table

Syllabus
2017
Topic
—
Level
AS

Atoms contain a tiny nucleus and surrounding electrons

An atom has a very small, dense nucleus containing protons and neutrons. Electrons occupy regions outside the nucleus, so nearly all the atom's mass is concentrated in the nucleus while the electron cloud accounts for most of its volume.

Protons identify the element. Neutrons add nuclear mass without changing the element's identity. Electrons are attracted to the positive nucleus and are arranged in energy levels and sub-shells; their arrangement later explains bonding and chemical behaviour.

A neutral atom has equal numbers of protons and electrons, so its positive and negative charges cancel. Changing the number of electrons makes an ion; changing the number of neutrons makes another isotope of the same element.

Do not picture electrons as miniature planets on fixed circular paths. The syllabus model places them in orbitals—regions associated with allowed energies—outside the nucleus.

Subatomic particles differ in charge and relative mass

Relative values compare the three subatomic particles without assigning their masses in kilograms or charges in coulombs. Proton charge is the positive reference and proton mass is approximately the mass reference.

Particle Relative charge Relative mass Location
proton +1+1 11 nucleus
neutron 00 11 nucleus
electron −1-1 about 1/18361/1836 outside the nucleus

An electric field deflects protons and electrons because they are charged, but it does not deflect neutrons. Electron mass is so small compared with nucleon mass that mass number counts protons and neutrons only.

Relative mass 11 does not mean a proton and neutron have exactly identical physical masses; it is the precision used in this atomic-accounting model.

Atomic number identifies an element; mass number counts nucleons

The atomic number, ZZ, is the number of protons in an atom's nucleus. It uniquely identifies the element. The mass number, AA, is the total number of protons and neutrons in one particular atom or ion.

^{A}_{Z}\mathrm{X}

In 3684Kr^{84}_{36}\ce{Kr}, Z=36Z=36, so the element is krypton and its nucleus contains 36 protons. A=84A=84 means the nucleus contains 84 nucleons in total. Mass number is always a whole number for one isotope.

Mass number is not relative atomic mass. Mass number describes one isotope and is integral; relative atomic mass is a weighted mean for an element's naturally occurring isotopes and is often non-integral.

Use $A$, $Z$ and ionic charge to count particles

Particle counts follow directly from isotope notation and charge. Protons equal ZZ, neutrons equal A−ZA-Z, and electrons are adjusted from ZZ by the signed ionic charge.

p=Z\qquad n=A-Z\qquad e=Z-q

Here qq is the ion charge in elementary-charge units: q=+2q=+2 for a 2+2+ ion and q=−1q=-1 for a 1−1- ion. Subtracting a negative charge therefore adds an electron.

Species Protons Neutrons Electrons
3276Ge^{76}_{32}\ce{Ge} 32 44 32
3476Se^{76}_{34}\ce{Se} 34 42 34
1735ClX−^{35}_{17}\ce{Cl-} 17 18 18

Ion formation changes only the electron count. It does not change ZZ, AA, proton number or neutron number; a nuclear change would be required to change the element or isotope.

Isotopes share proton number but differ in neutron number

Isotopes are atoms of the same element with the same number of protons but different numbers of neutrons. They therefore have the same atomic number but different mass numbers.

35Cl^{35}\ce{Cl} and 37Cl^{37}\ce{Cl} both contain 17 protons. They contain 18 and 20 neutrons respectively. Neutral atoms of both isotopes contain 17 electrons and therefore have the same ground-state electronic configuration.

Because chemical reactions mainly involve electrons, isotopes of an element have very similar chemical properties. Their different masses can produce different physical behaviour and separate peaks in a mass spectrum.

An isotope is an atom, not a different element and not an average. Relative atomic mass combines the masses and abundances of all isotopes in a sample.

A mass spectrum separates ions by mass-to-charge ratio

A mass spectrometer converts a sample into positive gaseous ions, accelerates them, separates them according to mass-to-charge ratio m/zm/z, and detects their relative abundance. Each peak position gives an m/zm/z value; peak height or area gives relative abundance.

  1. Introduce and vaporise the sample where necessary.
  2. Ionise particles to form positive ions.
  3. Accelerate ions using an electric field.
  4. Separate ions because different m/zm/z values respond differently or take different flight times.
  5. Detect ions and convert the signal into a spectrum.

A_r=\frac{\sum(\text{isotope mass}\times\text{relative abundance})}{\sum\text{relative abundance}}

Elemental peaks reveal isotope masses and abundances; the weighted mean gives ArA_r, and the equation can be rearranged to find an unknown abundance or mass. For a molecule, the molecular-ion peak gives its relative molecular mass when z=1z=1, helping identify the molecule. Fragment peaks represent smaller ions.

A 2+2+ ion has z=2z=2, so it appears at half the m/zm/z of the corresponding singly charged ion. A peak at m/z=20m/z=20 could therefore be a mass-20 ion with charge 1+1+ or a mass-40 ion with charge 2+2+; charge must be considered before assigning mass.

Diatomic molecular-ion peaks follow isotope probabilities

A diatomic molecule can contain every allowed pair of its element's isotopes. Add the isotope mass numbers to locate each molecular-ion peak, then multiply isotope probabilities to predict relative peak heights.

For two different isotopes, count both arrangements: 35Cl^{35}\ce{Cl}-37Cl^{37}\ce{Cl} and 37Cl^{37}\ce{Cl}-35Cl^{35}\ce{Cl}. This factor of two is why the mixed-isotope peak is larger than either single arrangement alone.

ClX2X+\ce{Cl2+} isotopologue m/zm/z probability for 75% 35Cl^{35}\ce{Cl} and 25% 37Cl^{37}\ce{Cl}
35Cl^{35}\ce{Cl}-35Cl^{35}\ce{Cl} 70 0.752=0.56250.75^2=0.5625
mixed pair 72 2(0.75)(0.25)=0.3752(0.75)(0.25)=0.375
37Cl^{37}\ce{Cl}-37Cl^{37}\ce{Cl} 74 0.252=0.06250.25^2=0.0625

Dividing by the smallest probability gives relative heights 9:6:19:6:1 at m/zm/z 70, 72 and 74. These are molecular-ion peaks, not the separate atomic-ion peaks at 35 and 37.

Successive ionisation energies remove electrons from gaseous ions

The first ionisation energy is the energy required to remove one electron from each atom in one mole of gaseous atoms, forming one mole of gaseous 1+1+ ions. Successive ionisation energies repeat this process from increasingly positive gaseous ions.

\ce{X(g) -> X+(g) + e-}\n\n\ce{X+(g) -> X^{2+}(g) + e-}\n\n\ce{X^{2+}(g) -> X^{3+}(g) + e-}

The equations define first, second and third ionisation energies respectively. Values are quoted per mole, usually in kJ mol−1\mathrm{kJ\,mol^{-1}}, and the starting species must be gaseous in every case.

All ionisation energies are endothermic: energy must be supplied to overcome electrostatic attraction between the negatively charged electron and the positive nucleus. Successive values generally rise because the remaining ion is more positively charged.

An orbital holds at most two opposite-spin electrons

An orbital is a region within an atom that can hold up to two electrons with opposite spins. It is associated with a particular energy and spatial distribution, not a fixed path around the nucleus.

An empty orbital holds no electrons; a singly occupied orbital holds one; a full orbital holds a pair. When two electrons share an orbital, their spins must be opposite, represented in electron-in-box notation by arrows pointing in opposite directions, ↑↓\uparrow\downarrow.

Orbitals are grouped into sub-shells. An s sub-shell contains one orbital, a p sub-shell three orbitals and a d sub-shell five orbitals. Orbital capacity therefore controls sub-shell capacity.

Opposite arrows describe opposite spin states; they do not mean that electrons literally rotate around the nucleus in opposite directions.

Ionisation energy balances nuclear attraction and electron environment

Ionisation energy is higher when the electron removed experiences stronger attraction to the nucleus. Compare nuclear charge, shielding, distance and the energy of the occupied sub-shell rather than citing only one factor.

Change Effect on attraction and ionisation energy
more protons at similar shielding and distance stronger attraction; ionisation energy rises
more inner-shell shielding weaker effective attraction; ionisation energy falls
electron farther from nucleus weaker attraction; ionisation energy falls
electron in a higher-energy, more shielded sub-shell easier to remove; ionisation energy falls

A 2p electron is higher in energy and more shielded than a 2s electron, explaining why boron's first ionisation energy is lower than beryllium's despite boron having more protons. Within 2p, repulsion in a paired orbital makes an electron easier to remove from oxygen than from nitrogen's singly occupied 2p orbitals.

Greater nuclear charge does not guarantee a higher ionisation energy when shielding, distance or sub-shell changes at the same time. State the competing effects and identify which dominates.

Ionisation-energy patterns reveal shells and sub-shells

Ionisation-energy data provided evidence that electrons occupy groups of distinct energies. Large and repeating changes cannot be explained by a uniform cloud of equivalent electrons.

For one element, successive ionisation energies rise, but a very large jump occurs after all electrons in the outer shell have been removed. The next electron comes from an inner shell, closer to the nucleus and less shielded. For a main-group element, the number of electrons removed before the first large jump identifies its group.

Across successive elements, first ionisation energy generally rises within a period as nuclear charge increases. A large fall after a noble gas shows the start of a new shell. Smaller falls, such as Be to B and Mg to Al, show entry into a higher-energy p sub-shell; the N to O and P to S falls show the effect of pairing within p orbitals.

A large jump in successive ionisation energies locates a shell boundary; a smaller irregularity across elements can identify a sub-shell or pairing effect. Do not interpret every numerical change as a new shell.

s orbitals are spherical; p orbitals have two lobes

An s orbital is spherical around the nucleus. A p orbital has two lobes on opposite sides of the nucleus, with a nodal plane through the nucleus where the probability of finding an electron is zero.

Each p sub-shell contains three orbitals of the same basic shape and energy, oriented along mutually perpendicular axes. They are labelled pxp_x, pyp_y and pzp_z. Each orientation is a different orbital and can hold up to two opposite-spin electrons.

The boundary shape represents a region of high probability for locating an electron; it is not a solid surface. The two p lobes belong to one orbital, not two separate orbitals.

A flat drawing of an s orbital may look circular, but its three-dimensional shape is spherical. A p orbital is not simply a figure-eight path travelled by an electron.

Electrons occupy equal-energy orbitals singly before pairing

Within a sub-shell, electrons enter separate orbitals one at a time before any pairing occurs. The singly occupying electrons have parallel spins. Only after every available orbital is singly occupied do additional electrons pair with opposite spin.

Configuration Electron-in-box pattern for the p sub-shell Meaning
p2p^2 [↑][↑][ ][\uparrow][\uparrow][\ ] two singly occupied orbitals
p3p^3 [↑][↑][↑][\uparrow][\uparrow][\uparrow] all three singly occupied
p4p^4 [↑↓][↑][↑][\uparrow\downarrow][\uparrow][\uparrow] one pair and two singles

Single occupation keeps electrons apart while the orbitals have equal energy. When two electrons share an orbital, opposite spins are required. The order of equivalent boxes does not matter; the occupancy pattern does.

Do not pair electrons in one p orbital while another equal-energy p orbital is empty. Do not draw two parallel-spin electrons in the same orbital.

Build electron configurations through krypton and adjust ions correctly

For ground-state atoms from H to Kr, add the atomic-number count of electrons in increasing orbital energy while respecting orbital capacity and single occupation before pairing.

1s;2s;2p;3s;3p;4s;3d;4p

Use superscripts for electron counts: s holds 2, p holds 6 and d holds 10. For example, sulfur is 1s22s22p63s23p41s^2 2s^2 2p^6 3s^2 3p^4; electron-in-box notation shows one paired and two singly occupied 3p orbitals. Noble-gas shorthand may replace completed inner shells.

Chromium and copper use the observed configurations [Ar]3d54s1[\ce{Ar}]3d^5 4s^1 and [Ar]3d104s1[\ce{Ar}]3d^{10}4s^1. For ions, add electrons for negative charge and remove them for positive charge from the highest principal shell first: transition-metal ions lose 4s electrons before 3d electrons. Thus FeX3+\ce{Fe^{3+}} is [Ar]3d5[\ce{Ar}]3d^5 and ClX−\ce{Cl-} is [Ar][\ce{Ar}].

The order used to fill neutral atoms is not always the order used to remove electrons from ions. Check the final electron total against atomic number and charge.

Outer electron configuration drives chemical properties

Chemical reactions rearrange outer electrons, so an element's electronic configuration controls the ions it tends to form, the bonds it makes and many patterns in its reactivity.

Elements in the same group have the same pattern of outer-shell electrons. Group 1 atoms have an outer ns1ns^1 electron and commonly form 1+1+ ions by losing it. Group 17 atoms have outer ns2np5ns^2np^5 configurations and need one more electron for a filled outer shell, so they commonly form 1−1- ions or one covalent bond.

Moving across a period changes the outer configuration one electron at a time, producing a systematic change from metallic to non-metallic behaviour. Moving down a group preserves the valence pattern but adds shells, so chemical behaviour remains related while reactivity can change.

Similar outer configurations explain similar chemistry, not identical properties. Nuclear charge, shielding and atomic size change between group members and modify reaction energetics.

Periodic-table blocks identify the sub-shell being filled

An element belongs to the s, p or d block according to the sub-shell receiving its differentiating electron in the ground-state configuration. Block widths follow the number of available orbitals.

Sub-shell Orbitals Maximum electrons First shell in which it occurs Periodic-table block width
s 1 2 n=1n=1 2
p 3 6 n=2n=2 6
d 5 10 n=3n=3 10

In the first four quantum shells, the relevant sub-shells are 1s1s; 2s,2p2s,2p; 3s,3p,3d3s,3p,3d; and 4s,4p,4d4s,4p,4d. Each s, p or d sub-shell always has the same capacity regardless of its shell number.

Period number and block label answer different questions. For example, the 3d sub-shell is filled across Period 4 because 4s is occupied first in neutral atoms.

Graphs expose repeating periodic patterns

A periodic property shows a pattern that repeats as atomic number increases because similar outer electron configurations recur. Plotting data for elements 1–36 makes repeated rises, falls and turning points visible across successive periods.

Use atomic number on the horizontal axis so the elements are in sequence. Label the vertical axis with the property and its unit, choose a scale that uses the plotting area effectively, plot each value accurately, and join points only when the purpose is to display the sequence rather than imply continuous values between elements.

For a logarithmic treatment, calculate log⁡10\log_{10} of each first-ionisation-energy value and plot that transformed value against atomic number. Label the axis to show both the logarithm and the original energy unit convention. Equal vertical intervals then represent equal ratios in first ionisation energy, not equal raw-energy differences, which can make repeated proportional features easier to compare.

A graph is evidence of periodicity only when the pattern recurs with atomic number. One local rise or fall is a trend, not by itself a periodic property; connect repeated features to repeating electron configurations.

Structure and electron attraction explain Period 2 and 3 trends

Periodic trends are consequences of structure and electron configuration. Melting and boiling involve overcoming bonding or intermolecular forces, whereas ionisation involves removing an electron from a gaseous atom.

Region of Periods 2 and 3 Structure and trend explanation
Li–Be and Na–Al giant metallic lattices; higher cation charge, more delocalised electrons and smaller ions strengthen metallic bonding, generally raising melting/boiling temperatures
B/C and Si giant covalent structures; many strong covalent bonds must be broken, giving high values
NX2\ce{N2}, OX2\ce{O2}, FX2\ce{F2}, PX4\ce{P4}, SX8\ce{S8}, ClX2\ce{Cl2} and noble gases simple molecular or monatomic substances; only London forces are overcome, so values are much lower and generally increase with electron-cloud size; SX8\ce{S8} is notably higher than smaller Period 3 molecules

Across each period, first ionisation energy generally increases because proton number rises while added electrons enter the same main shell, so shielding changes little and atomic radius decreases. The Group 13 dip occurs when the electron removed is in a higher-energy p sub-shell; the Group 16 dip occurs because repulsion in a paired p orbital makes removal easier than from the preceding half-filled p sub-shell.

Down a group, first ionisation energy decreases. The outer electron occupies a higher shell, farther from the nucleus, and experiences more inner-shell shielding. These effects outweigh the increased proton number, weakening attraction to the electron removed.

Do not explain melting-point trends with ionisation energy or atomic radius alone: first identify metallic, giant covalent, molecular or monatomic structure and the attraction that must be overcome.

Topic 3: Bonding and Structure

Syllabus
2017
Topic
—
Level
AS

Three kinds of evidence reveal ions

Ions are charged particles. No single observation is the whole model: physical properties, electron-density evidence and migration together support the existence of oppositely charged particles in ionic substances.

Evidence Observation Ionic interpretation
Physical properties Ionic solids usually have high melting temperatures, are brittle, do not conduct as solids, but conduct when molten or dissolved Strong attractions hold a lattice; charged ions become mobile only when the lattice is broken or the solid dissolves
Electron-density map Electron density is concentrated around separate positive and negative ion centres rather than shared evenly between adjacent atoms Electron transfer has produced distinguishable ions
Migration In an electric field, cations move to the negative electrode and anions to the positive electrode The particles carry opposite charges

For a coloured solution containing a blue cation and a yellow anion, movement of the two colours towards opposite electrodes is especially direct migration evidence. A complete circuit and an ion-conducting path are needed for the observation.

Conductivity alone does not prove that a solid contains mobile ions: metals conduct through delocalised electrons. Interpret the full pattern of evidence and the state of the substance.

Ions form when atoms lose or gain electrons

An atom becomes an ion by changing its number of electrons. Losing electrons leaves more protons than electrons and forms a cation; gaining electrons gives more electrons than protons and forms an anion.

Process Electron equation Check
sodium loses one electron Na→Na++e−\mathrm{Na \rightarrow Na^+ + e^-} charge changes from 0 to +1
magnesium loses two electrons Mg→Mg2++2e−\mathrm{Mg \rightarrow Mg^{2+} + 2e^-} charge changes from 0 to +2
chlorine gains one electron Cl+e−→Cl−\mathrm{Cl + e^- \rightarrow Cl^-} charge changes from 0 to −1
oxygen gains two electrons O+2e−→O2−\mathrm{O + 2e^- \rightarrow O^{2-}} charge changes from 0 to −2

Balance both the number of atoms and the total charge. The electron is on the product side for electron loss and on the reactant side for electron gain.

Ion formation in chemical reactions changes electrons, not the number of protons. Changing proton number would change the element.

Dot-and-cross diagrams account for ionic electrons

A dot-and-cross diagram tracks the outer-shell electrons supplied by different atoms. Dots and crosses show electron origin; they do not represent different kinds of electron.

First determine the ions and their simplest whole-number ratio. Draw each ion in square brackets, show its outer shell after transfer, and write the charge outside the bracket. Repeat each ion the number of times required by the formula.

Compound Cations to draw Anions to draw Outer-shell result
NaCl\mathrm{NaCl} one [Na]+[\mathrm{Na}]^+ one [Cl]−[\mathrm{Cl}]^- Na+^+ has lost its outer electron; Cl−^- has eight outer electrons
MgCl2\mathrm{MgCl_2} one [Mg]2+[\mathrm{Mg}]^{2+} two [Cl]−[\mathrm{Cl}]^- each chloride has one transferred electron
Al2O3\mathrm{Al_2O_3} two [Al]3+[\mathrm{Al}]^{3+} three [O]2−[\mathrm{O}]^{2-} each oxide has eight outer electrons

Do not draw a shared pair or a line between ionic particles. The diagram shows electron transfer and ion charges, not a small covalent molecule.

An ionic crystal is a giant repeating lattice

An ionic crystal contains a three-dimensional, regularly repeating arrangement of cations and anions. Each ion is surrounded by ions of opposite charge in a pattern that extends throughout the crystal.

In a two-dimensional section, show alternating positive and negative ions in both row and column directions. A three-dimensional lattice continues the alternation through additional layers; the exact coordination depends on the compound.

The chemical formula gives the lowest whole-number ratio of ions needed for electrical neutrality. For example, NaCl means a 1:1 ratio and CaCl2_2 means a 1:2 ratio across the giant lattice.

An ionic formula such as NaCl does not identify one separate NaCl molecule. It states the ion ratio in the extended lattice.

Ionic bonding is net attraction through a lattice

Ionic bonding is the strong net electrostatic attraction between oppositely charged ions.

Every ion interacts with many surrounding ions. Opposite charges attract and like charges repel, but at the stable lattice spacing the overall arrangement has a strong net attraction and lower energy than widely separated ions.

The attraction acts in all directions through the giant lattice. This helps explain why separating ions requires substantial energy rather than breaking one isolated link.

Do not define an ionic bond as electron transfer. Transfer explains ion formation; the bond itself is electrostatic attraction between the ions after they form.

Charge and distance control ionic attraction

Ionic attraction becomes stronger when the charges are larger and when the distance between ion centres is smaller. Ionic radius affects that separation: smaller ions can approach more closely.

Change, with other factors comparable Effect on attraction Reason
+1+1 cation replaced by +2+2 cation stronger larger charge product
large cation replaced by smaller cation stronger smaller centre-to-centre distance
−1-1 anion replaced by −2-2 anion stronger larger charge product

BaCl2_2 has stronger ionic attraction than CsCl because Ba2+^{2+} has a higher charge and is smaller than Cs+^+. More energy is therefore needed to separate its ions, consistent with its higher melting temperature.

When comparing real melting temperatures, control both charge and radius and remember that lattice structure can also matter. Do not use charge alone if ion sizes differ.

Ionic-radius trends follow shells and nuclear charge

For ions with the same charge down a group, ionic radius increases. Each step adds an occupied electron shell; the greater distance and shielding outweigh the increased nuclear charge.

Ion Protons Electrons Relative position in the sequence
N3−\mathrm{N^{3-}} 7 10 largest
O2−\mathrm{O^{2-}} 8 10 smaller
F−\mathrm{F^-} 9 10 smaller
Na+\mathrm{Na^+} 11 10 smaller
Mg2+\mathrm{Mg^{2+}} 12 10 smaller
Al3+\mathrm{Al^{3+}} 13 10 smallest

All ions from N3−^{3-} to Al3+^{3+} are isoelectronic: they have ten electrons and the same occupied-shell pattern. As proton number increases, the same electron cloud experiences stronger nuclear attraction, so radius decreases.

Do not explain the isoelectronic sequence by changing electron-shell number: it is constant across this set. The changing variable is nuclear charge.

Polarisation is distortion of an ion's electron cloud

Polarisation occurs when a cation attracts and distorts the electron cloud of a neighbouring anion.

The anion's electrons are drawn towards the cation, so the electron distribution is no longer symmetrical. Greater distortion increases electron density between the nuclei and gives the bonding more covalent character.

The cation has polarising power; the anion is polarisable. These terms describe the ability to cause distortion and the ease of being distorted, respectively.

Polarisation of an ion is electron-cloud distortion. It is not the same as making an entire molecule polar, which depends on bond dipoles and molecular shape.

Ion size and charge govern polarisation

Particle property Consequence Explanation
small cation greater polarising power its positive charge is concentrated close to the anion
cation with higher positive charge greater polarising power it attracts the anion's electrons more strongly
large anion greater polarisability outer electrons are farther from their nucleus and more shielded
anion with greater negative charge, for a sensible comparison usually greater polarisability the larger, more electron-rich cloud is more readily distorted

The greatest distortion is expected when a small, highly charged cation is next to a large, highly charged anion. The bonding then shows more covalent character than a simple ionic model predicts.

F−^- is difficult to polarise because it is small and carries only a single negative charge. Al3+^{3+} has much greater polarising power than Na+^+ because it is smaller and has a higher charge.

State whether you are discussing polarising power of a cation or polarisability of an anion; they are related but not interchangeable properties.

A shared electron pair attracts two nuclei

A covalent bond is the strong electrostatic attraction between two nuclei and a shared pair of electrons between them.

Evidence Observation Covalent interpretation
Electron-density map of a simple molecule increased electron density lies between bonded nuclei the bonding pair is shared between the atoms
Giant atomic structure very high melting temperature and hardness are common; most do not conduct many strong covalent bonds extend through a giant network and require much energy to break

Both nuclei attract the negatively charged shared pair. A stable bond length is reached where the attractions lower the energy while nucleus–nucleus and electron–electron repulsions prevent collapse.

Covalent bonding is not simply 'atoms sharing electrons'. The defining force is electrostatic attraction between the shared pair and both nuclei.

Dot-and-cross diagrams show shared and donated pairs

Show outer-shell electrons only, using one symbol for electrons from each starting atom. A single, double or triple bond contains one, two or three shared pairs. Add every lone pair needed to complete the outer-shell accounting.

Species What the diagram must show
H2_2, O2_2, N2_2 one, two and three shared pairs respectively
NH4+_4^+ NH3_3 donates its nitrogen lone pair to H+^+; enclose the resulting ion in brackets with an overall + charge
Al2_2Cl6_6 two bridging chlorines; for each bridge, a chlorine lone pair is donated to an electron-deficient aluminium centre

In a dative covalent bond, both electrons in the shared pair originally come from the same donor atom. Once formed, the pair is attracted to both nuclei like any other covalent bond.

Dots and crosses record electron origin, not charge. Do not omit lone pairs or overall brackets and charge when drawing an ion such as NH4+_4^+.

Carbon lattices link structure to application

Allotrope Structure and bonding Key properties Example applications
diamond each C forms four covalent bonds in a rigid 3D tetrahedral lattice very hard, high melting temperature, no mobile electrons cutting and abrasive tools
graphite each C forms three bonds in planar hexagonal layers; one electron per C is delocalised; weak forces act between layers conducts along layers; layers slide; high melting temperature electrodes, lubricants
graphene one atom-thick hexagonal sheet; each C forms three bonds with delocalised electrons across the sheet strong, light and electrically conducting conductive electronics and reinforcing composites

Applications follow from structure: continuous strong bonds resist deformation, delocalised electrons carry charge, and weak attractions between graphite layers allow sliding.

Graphite is not soft because its covalent bonds are weak. Strong bonds hold each layer; softness comes from weak attractions between layers.

Electronegativity measures attraction for a bonding pair

Electronegativity is the ability of an atom in a covalent bond to attract the shared pair of electrons towards itself.

If two bonded atoms have different electronegativities, the more electronegative atom attracts the pair more strongly and becomes partially negative, δ−\delta-; the other becomes partially positive, δ+\delta+.

Electronegativity is used comparatively. The difference between the two bonded atoms, rather than either value by itself, helps predict how unevenly the pair is shared.

Electronegativity is not an atom's charge and it is not the same as electron affinity. It describes an atom while it is covalently bonded.

Bonding lies on an ionic–covalent continuum

Covalent and ionic bonding are limiting models on a continuum. As the electronegativity difference between bonded atoms increases, electron sharing becomes more unequal: bond polarity and ionic character increase.

Electronegativity difference Useful description Electron distribution
zero or very small non-polar covalent shared nearly equally
intermediate polar covalent shifted towards the more electronegative atom, producing partial charges
very large predominantly ionic described mainly as oppositely charged ions

Using Ba 0.9, Be 1.5 and Cl 3.0, ΔEN\Delta EN is 2.1 for Ba–Cl but 1.5 for Be–Cl. BaCl2_2 therefore has more ionic character, while BeCl2_2 has more covalent character.

Do not treat one numerical cut-off as a universal switch. Electronegativity difference supports a continuum comparison; polarisation and structure also refine the model.

Polar bonds do not always make a polar molecule

A polar bond has unequal electron sharing and a bond dipole. A polar molecule has a non-zero resultant dipole after all bond dipoles are combined as vectors.

Step Question to ask
1 Which bonds are polar, and towards which atom does each dipole point?
2 What is the molecule's three-dimensional shape?
3 Do equal dipoles cancel by symmetry, or is there a non-zero resultant?

CO2_2 has two polar C=O bonds but is linear, so equal opposing dipoles cancel and the molecule is non-polar. H2_2O is bent, so its O–H dipoles do not cancel and the molecule is polar. Symmetrical BF3_3 and CCl4_4 are also non-polar despite polar bonds.

A molecule is not automatically polar because it contains polar bonds. Shape and symmetry decide whether the vector sum is zero.

Electron regions arrange for maximum separation

Electron pairs around a central atom repel one another and adopt an arrangement that keeps them as far apart as possible. Both bonding pairs and lone pairs must be counted.

Step Action
1 draw or infer the central atom's bonding and lone pairs
2 count regions of electron density; a single, double or triple bond counts as one region
3 arrange all regions for maximum separation
4 name the molecular shape from atom positions, then adjust angles for lone-pair repulsion

Repulsion strength follows lone pair–lone pair > lone pair–bond pair > bond pair–bond pair because a lone pair is held by only one nucleus and occupies more space near the central atom.

Electron-region geometry includes lone pairs, but the named molecular shape uses only atom positions. Do not count a double bond as two separate directions.

Bond length is a distance; bond angle is an angle

Bond length is the equilibrium distance between the nuclei of two bonded atoms. It is commonly measured in picometres or nanometres.

Bond angle is the angle between two bonds that meet at the same central atom. The three atoms defining it must be identified; for H–O–H, oxygen is the vertex.

A bond length is an equilibrium value because attraction and repulsion balance at the minimum-energy separation. Bond angles describe the spatial arrangement produced by electron-region repulsions.

Bond length is not the distance between electron pairs, and a bond angle cannot be assigned without specifying the central atom and the two bond directions.

Required molecules follow electron-pair geometry

Species Central electron regions Shape Bond angle(s)
BeCl2_2 2 bonding, 0 lone linear 180°
BCl3_3 3 bonding, 0 lone trigonal planar 120°
CH4_4 4 bonding, 0 lone tetrahedral 109.5°
NH3_3 3 bonding, 1 lone trigonal pyramidal 107°
NH4+_4^+ 4 bonding, 0 lone tetrahedral 109.5°
H2_2O 2 bonding, 2 lone bent 104.5°
CO2_2 2 bonding, 0 lone linear 180°
PCl5_5(g) 5 bonding, 0 lone trigonal bipyramidal 90°, 120°, 180°
SF6_6 6 bonding, 0 lone octahedral 90°, 180°
C2_2H4_4 3 regions at each C trigonal planar around each C; molecule planar about 120°

For two to six regions with no lone pairs, maximum separation gives linear, trigonal planar, tetrahedral, trigonal bipyramidal and octahedral arrangements. Lone pairs compress bond angles: CH4_4 109.5° becomes NH3_3 107° and H2_2O 104.5° as lone pairs are added.

The C=C double bond in ethene is one electron region around each carbon. Do not count it twice when predicting the trigonal-planar arrangement.

Apply the same repulsion method to analogous species

For an unfamiliar molecule or ion, determine the central atom's bonding pairs, lone pairs and overall charge, then use the same electron-region patterns as the required examples. Analogy means the same relevant region count, not merely a similar formula.

Unfamiliar species Electron-region analogy Prediction
CS2_2 CO2_2: two bonding regions linear, 180°
BF4−_4^- CH4_4/NH4+_4^+: four bonding regions tetrahedral, 109.5°
PH3_3 NH3_3: three bonding regions and one lone pair trigonal pyramidal; angle less than 109.5°
SO2_2 three regions, one of them a lone pair bent; angle less than 120°

Include the ion's charge when counting electrons. After arranging all electron regions, ignore lone-pair positions when naming the molecular shape.

Do not copy an exact bond angle from an analogy when different atoms or multiple bonds alter repulsion. Use ideal angles where appropriate and state a justified 'less than' prediction when lone pairs compress them.

A metal is an ion lattice in delocalised electrons

A metal consists of a giant, regular lattice of positive metal ions surrounded by a sea of delocalised electrons.

Outer electrons are no longer attached to one particular atom or one ion–ion pair. They move throughout the lattice, while the total negative charge of the electrons balances the total positive charge of the ions.

In a particle diagram, show closely packed positive ions in repeating layers and many electrons distributed between them. The diagram represents a continuous giant structure, not separate molecules.

The lattice positions are occupied by positive metal ions, not neutral atoms. The delocalised electrons remain part of the metal and preserve overall electrical neutrality.

Metallic bonding is non-directional electrostatic attraction

Metallic bonding is the strong electrostatic attraction between positive metal ions and delocalised electrons.

Each ion is attracted to the shared electron sea around many ions. The attraction is non-directional and extends throughout the giant lattice.

More delocalised electrons per ion and a higher ion charge can strengthen the attraction; smaller metal ions also bring charge centres closer, when other structural factors are comparable.

Metallic bonding is not attraction between positive ions, which would repel. The delocalised electrons provide the negative charge attracted to the ions.

The metallic model explains conductivity and melting

Property Model-based explanation
electrical conductivity delocalised electrons are mobile and carry charge through the lattice when a potential difference is applied
high melting temperature much energy is needed to weaken the strong attraction between positive ions and delocalised electrons throughout the giant lattice
malleability layers of ions can shift while remaining attracted to the non-directional electron sea, so the structure can change shape without immediately shattering

Magnesium usually has stronger metallic bonding than sodium because each Mg atom contributes two delocalised electrons and forms Mg2+^{2+}, whereas sodium contributes one and forms Na+^+; Mg2+^{2+} is also smaller. The attraction is therefore stronger and more energy is required to overcome it.

Metals conduct as solids and when molten because their charge carriers are electrons, which remain mobile in both states. This contrasts with an ionic solid, whose ions are fixed until it melts or dissolves.

Do not say that heating 'breaks metal ions'. Melting weakens enough metallic attraction for the ordered lattice to lose its fixed structure; the ions themselves remain ions.

Topic 4: Introductory Organic Chemistry AS and Alkanes

Syllabus
2017
Topic
—
Level
AS

A hazard is inherent; risk depends on exposure

Term Meaning What can change?
hazard the inherent potential of a substance or procedure to cause harm the hazard classification normally remains fixed for that substance and use
risk the likelihood and possible severity of harm under particular conditions amount, concentration, exposure route, duration and controls can all change it

Concentrated hydrochloric acid is corrosive: that is its hazard. Using a large open beaker near eye level creates a higher risk than handling a few drops in a tray while wearing eye protection, because exposure is more likely or consequential.

Risk assessment therefore asks: what harm can occur, who or what could be exposed, how likely and severe is it, and which controls reduce that risk to an acceptable level?

A control measure reduces risk; it does not usually remove the chemical's inherent hazard. Do not use 'hazard' and 'risk' as synonyms.

Organic-chemistry hazards require a risk assessment

Common organic-chemistry hazard Possible source Potential harm
flammable volatile solvents and fuels ignition, fire and burns
harmful or toxic vapours, products or reagents harm by inhalation, ingestion or skin exposure
corrosive strong acids or alkalis used with organic substances tissue and eye damage
irritant some vapours and liquids skin, eye or respiratory irritation
environmental hazard persistent or toxic releases harm to organisms and ecosystems

A risk assessment identifies the substances, quantities, concentrations, temperatures, apparatus, exposure routes and people involved. It then selects controls, records emergency action and considers disposal before work begins.

Organic compounds are often volatile and flammable, so vapour can spread beyond the vessel and meet an ignition source. The same chemical can present very different risks at microscale and at bulk scale.

A hazard pictogram identifies a class of harm; it does not by itself state the risk of the planned procedure. Conditions and controls must also be assessed.

Reduce risk by changing scale, controls or method

Risk-reduction route Example Why risk falls
work on a smaller scale use millilitres rather than tens of millilitres less material and energy are available if something goes wrong
take hazard-specific precautions use a fume cupboard for toxic vapour; exclude flames for a flammable solvent; wear eye protection for splashes the control blocks the relevant exposure or ignition route
use a less hazardous method replace a toxic or highly flammable reagent where a suitable safer alternative exists the initiating hazard is reduced or removed

Prefer controls that remove or contain the hazard before relying only on personal protective equipment. Check ventilation, heating method, secure apparatus, spill response and waste route for the actual procedure.

For carbon monoxide, improve containment and ventilation, use a fume cupboard or suitable extraction, monitor where necessary, and limit exposure time. Gloves alone do not control an inhalation hazard.

A generic precaution is not enough: the control must match the hazard and exposure route. A smaller scale reduces consequences but does not make unsafe technique acceptable.

A homologous series shares a functional group

A homologous series is a family of organic compounds with the same functional group and general formula, similar chemical reactions, and a gradual trend in physical properties. Successive members differ by CH2_2.

A functional group is the atom or group of atoms responsible for the characteristic reactions of an organic compound. Examples include C=C in alkenes, –OH in alcohols and –COOH in carboxylic acids.

Series Functional feature General formula for the relevant acyclic series
alkanes C–C and C–H single bonds only CnH2n+2\mathrm{C_nH_{2n+2}}
alkenes C=C CnH2n\mathrm{C_nH_{2n}}
alcohols –OH CnH2n+1OH\mathrm{C_nH_{2n+1}OH}

Members of a homologous series do not have identical physical properties: boiling temperature usually changes gradually with chain length. Similar chemistry comes from the shared functional group.

IUPAC names encode the longest chain and substituents

Carbon atoms 1 2 3 4 5 6 7 8 9 10
stem meth- eth- prop- but- pent- hex- hept- oct- non- dec-

Choose the longest parent chain containing the principal functional group and any required multiple bond. Number from the end giving the lowest relevant locants. Name and alphabetise substituents, use di-, tri- or tetra- for repeats, then add the suffix and locant for the functional group.

CH3_3C(CH3_3)2_2CH2_2CH(CH3_3)CH3_3 has a five-carbon parent chain and methyl groups at 2, 2 and 4, so its name is 2,2,4-trimethylpentane. Commas separate numbers and hyphens separate numbers from words.

Representation What must be shown
structural/condensed connectivity in grouped form, such as CH3_3CH2_2OH
displayed every atom and every bond
skeletal carbon-chain lines and vertices; C and attached H atoms are omitted, but heteroatoms and their H atoms are shown

The visually straightest line is not necessarily the longest carbon chain. Trace all connected carbon routes before selecting and numbering the parent.

Classify a reaction by its structural change

Reaction class Recognising change Example pattern
addition two reactants form one main product across a multiple bond C=C becomes C–C as atoms add
substitution one atom or group is replaced by another alkane H replaced by Cl
oxidation oxygen is gained or hydrogen is lost primary alcohol to aldehyde
reduction hydrogen is gained or oxygen is lost C=O to C–OH
polymerisation many monomers join to form a long-chain molecule many alkenes form an addition polymer

Compare bonds and functional groups in reactants and products. Classify the actual transformation, not the reagent name: converting C=C to C–C by adding atoms is addition, while replacing C–H by C–Cl is substitution.

A reaction can involve more than one change in a complex molecule. Name the class for the specified position or step rather than forcing the whole scheme into one label.

Bond fission can divide an electron pair equally or unequally

Bond breaking Electron movement Products Arrow convention
homolytic fission one bonding electron goes to each atom two free radicals two curly half-arrows, each moving one electron
heterolytic fission both bonding electrons go to one atom a cation and an anion a full curly arrow, moving an electron pair

Under ultraviolet light, Cl–Cl can split homolytically: Cl2→2Cl⋅\mathrm{Cl_2 \rightarrow 2Cl\boldsymbol{\cdot}}. H–Cl can be represented as breaking heterolytically to H+^+ and Cl−^- when both electrons go to chlorine.

After drawing arrows, count electrons and charges in every product. A radical has an unpaired electron; heterolysis produces opposite charges whose total equals the reactant charge.

Homolytic does not mean the bond breaks into ions. Equal electron division makes radicals; unequal division makes ions.

Radicals have an unpaired electron; electrophiles accept a pair

Species Definition Typical notation/example
free radical a species with an unpaired electron Cl⋅\boldsymbol{\cdot} or CH3_3$\boldsymbol{\cdot}$
electrophile an electron-pair acceptor H+^+ accepts a lone pair; Brδ+^{\delta+} can accept a pair during addition

The unpaired electron makes many radicals highly reactive. An electrophile is electron-deficient and is attracted to an electron-rich region such as a lone pair or a π\pi bond.

A radical is defined by an unpaired electron, not by having a charge. An electrophile accepts an electron pair; it need not carry a full positive charge.

Alkanes and cycloalkanes are saturated hydrocarbons

Family General formula Structural feature
acyclic alkane CnH2n+2\mathrm{C_nH_{2n+2}} open chain; C–C single bonds only
monocyclic cycloalkane CnH2n\mathrm{C_nH_{2n}} one carbon ring; C–C single bonds only

A hydrocarbon contains carbon and hydrogen only. Saturated means that it contains no carbon–carbon multiple bond, so each carbon has the maximum number of hydrogen atoms allowed by its C–C connectivity.

Closing an alkane chain to make one ring removes two hydrogen atoms, which explains the change from Cn_nH2n+2_{2n+2} to Cn_nH2n_{2n}. For example, propane is C3_3H8_8 and cyclopropane is C3_3H6_6.

Cn_nH2n_{2n} does not prove that a compound is a cycloalkane; an acyclic alkene can have the same general formula. Inspect the bonds and ring connectivity.

Structural isomers share a formula but differ in connectivity

Structural isomers are compounds with the same molecular formula but different structural formulae: their atoms are connected in different ways.

C4_4H10_{10} can be CH3_3CH2_2CH2_2CH3_3 (butane) or CH3_3CH(CH3_3)CH3_3 (2-methylpropane). Both contain four carbons and ten hydrogens, but the carbon skeletons differ.

To find isomers, vary the carbon skeleton, functional-group position or functional group where the formula permits it. After each drawing, recount atoms, check valencies, assign an IUPAC name and reject any structure that is just a rotated or renumbered duplicate.

Different orientations of the same connectivity are not structural isomers. A molecular formula alone also does not show which atoms are connected.

Enumerate alkane and cycloalkane isomers systematically

Formula Distinct alkane names
C4_4H10_{10} butane; 2-methylpropane
C5_5H12_{12} pentane; 2-methylbutane; 2,2-dimethylpropane
C6_6H14_{14} hexane; 2-methylpentane; 3-methylpentane; 2,2-dimethylbutane; 2,3-dimethylbutane

For a cycloalkane, choose a ring size from three up to the total carbon count, then distribute the remaining carbons as substituents. Number substituted rings to give the lowest set of locants and reject rotations, reflections and alternative numbering of the same connectivity.

C4_4H8_8 gives cyclobutane and methylcyclopropane. For C5_5H10_{10}, valid connectivities include cyclopentane, methylcyclobutane, ethylcyclopropane, 1,1-dimethylcyclopropane and 1,2-dimethylcyclopropane. This same ring-size method extends to six carbons.

Use displayed, structural or skeletal formulae consistently. In a skeletal ring, every unlabelled vertex is carbon and enough hydrogens are implied to give carbon four bonds.

Cis/trans forms have the same connectivity and are stereoisomers, not additional structural isomers. Do not double-count them in a structural-isomer list.

Crude oil is separated and converted into useful alkanes

Process What happens Chemical or physical? Example/evidence
fractional distillation hydrocarbons separate by boiling range in a temperature gradient physical separation lower-boiling fractions condense higher in the column
cracking long-chain molecules split into smaller, more useful molecules chemical reaction C10H22→C8H18+C2H4\mathrm{C_{10}H_{22} \rightarrow C_8H_{18}+C_2H_4}
reforming straight chains rearrange to branched, cyclic or aromatic products with improved fuel quality chemical reaction C6H14→C6H12+H2\mathrm{C_6H_{14} \rightarrow C_6H_{12}+H_2} for cyclisation with dehydrogenation

Alkanes burn exothermically, so fractions containing them are used as fuels. Supply and demand rarely match crude-oil composition, so cracking increases smaller fuels and alkene feedstocks, while reforming improves combustion quality.

For every cracking or reforming equation, conserve the number of carbon and hydrogen atoms. Fractional distillation has no reaction equation because no covalent bonds change.

Cracking does not simply separate an existing mixture: it breaks covalent bonds and makes new molecules. Fractional distillation separates without changing molecular identities.

Alkane combustion can release several pollutants

Pollutant How it arises during fuel use
carbon monoxide, CO incomplete combustion when oxygen is insufficient
carbon particulates (soot) very incomplete combustion of hydrocarbon fuel
unburned hydrocarbons fuel escapes combustion or burns incompletely
nitrogen oxides, NOx_x N2_2 and O2_2 from air react at high engine temperatures
sulfur oxides, SOx_x sulfur-containing impurities in fuel are oxidised

Pollutant formation depends on fuel composition and combustion conditions. Improving oxygen mixing can reduce CO and soot, but high combustion temperature can favour nitrogen-oxide formation.

Carbon monoxide is not produced because carbon is absent; it forms when carbon-containing fuel is only partially oxidised. Nitrogen oxides come mainly from air at high temperature, not from the alkane formula.

CO is toxic; nitrogen and sulfur oxides form acids

Pollutant Specified problem Causal explanation
carbon monoxide toxicity CO binds strongly to haemoglobin, reducing the blood's ability to transport oxygen
nitrogen oxides acidity they react with oxygen and water to form acidic solutions, contributing to acid deposition
sulfur oxides acidity they dissolve and oxidise in atmospheric water to form acids, contributing to acid deposition

Acid deposition lowers the pH of soils and surface waters and can damage carbonate stone and living systems. In an enclosed space, incomplete combustion makes CO especially dangerous because it is colourless and toxic.

For this objective, keep the causal claim precise: CO toxicity is explained through haemoglobin and reduced oxygen transport; the specified issue for nitrogen and sulfur oxides is their acidity.

Alternative fuels trade sustainability against emissions

Alternative fuels are developed to reduce dependence on finite crude oil, improve long-term security of supply and reduce harmful or greenhouse-gas emissions over the fuel's life cycle.

Criterion Question for comparison
resource sustainability Is the feedstock renewable, and how quickly is it replaced?
climate effect How much net CO2_2-equivalent is emitted from production, transport and use?
air quality Are CO, particulates, sulfur oxides or nitrogen oxides reduced?
practicality What energy density, storage, infrastructure, land and cost are required?

Combustion of fossil alkanes transfers geologically stored carbon to atmospheric CO2_2. CO2_2 absorbs outgoing infrared radiation, so increasing its concentration strengthens the greenhouse effect and contributes to climate change.

An alternative fuel is not automatically sustainable or low-carbon. Compare the complete production-and-use pathway, not tailpipe emissions alone.

Carbon neutrality is a life-cycle balance

A fuel is carbon neutral only if the amount of CO2_2 added to the atmosphere across its life cycle is balanced by CO2_2 removed or otherwise prevented from being added. The boundary must include production, processing and transport as well as use.

Fuel Carbon-neutrality judgment
petrol not carbon neutral: combustion releases fossil carbon, with further emissions from extraction and refining
bioethanol potentially close to neutral for biogenic carbon because growing plants absorb CO2_2, but farming, fertiliser, processing, transport and land-use change create additional emissions
hydrogen produces water and no CO2_2 at point of use, but neutrality depends on how H2_2 is made; renewable electrolysis can be low-carbon, fossil-fuel production is not

State the system boundary, identify every carbon or energy input, compare atmospheric uptake with emissions, and give a conditional conclusion rather than relying on a label such as 'bio' or 'hydrogen'.

Zero carbon at the exhaust is not the same as carbon neutral. Upstream energy and feedstock can dominate the life-cycle balance.

Alkanes undergo combustion and halogen substitution

Reaction Conditions and products Example
complete combustion excess oxygen; CO2_2 and H2_2O CH4+2O2→CO2+2H2O\mathrm{CH_4+2O_2 \rightarrow CO_2+2H_2O}
incomplete combustion limited oxygen; CO and/or C plus H2_2O 2CH4+3O2→2CO+4H2O\mathrm{2CH_4+3O_2 \rightarrow 2CO+4H_2O}
halogen substitution chlorine or bromine with ultraviolet light; an H atom is replaced by halogen CH4+Cl2→CH3Cl+HCl\mathrm{CH_4+Cl_2 \rightarrow CH_3Cl+HCl}

To balance complete combustion of Cx_xHy_y, form xxCO2_2 and y/2y/2H2_2O, then balance O2_2. Include state symbols when requested.

The carbon skeleton remains while a C–H bond and X–X bond are replaced by C–X and H–X bonds. Ultraviolet radiation initiates radical formation.

Halogen reaction with an alkane is substitution, not addition, because the saturated carbon skeleton has no C=C bond for addition across.

Free-radical substitution is a chain mechanism

Stage Methane/chlorine equation Role
initiation Cl2→UV2Cl⋅\mathrm{Cl_2 \xrightarrow{UV} 2Cl\boldsymbol{\cdot}} homolytic fission creates radicals; draw two curly half-arrows from Cl–Cl
propagation 1 Cl⋅+CH4→HCl+CH3⋅\mathrm{Cl\boldsymbol{\cdot}+CH_4 \rightarrow HCl+CH_3\boldsymbol{\cdot}} a radical is consumed and another radical formed
propagation 2 CH3⋅+Cl2→CH3Cl+Cl⋅\mathrm{CH_3\boldsymbol{\cdot}+Cl_2 \rightarrow CH_3Cl+Cl\boldsymbol{\cdot}} regenerates Cl⋅\boldsymbol{\cdot}, continuing the chain
termination Cl⋅+Cl⋅→Cl2\mathrm{Cl\boldsymbol{\cdot}+Cl\boldsymbol{\cdot} \rightarrow Cl_2}; CH3⋅+Cl⋅→CH3Cl\mathrm{CH_3\boldsymbol{\cdot}+Cl\boldsymbol{\cdot} \rightarrow CH_3Cl}; 2CH3⋅→C2H6\mathrm{2CH_3\boldsymbol{\cdot} \rightarrow C_2H_6} two radicals combine and no radical remains

A curly half-arrow moves one electron. In each propagation step, use half-arrows so bond breaking and bond formation account for the unpaired electron without inventing charge.

The product can undergo further substitution because it still contains C–H bonds. Longer alkanes can also substitute at different carbon positions. The resulting mixture of products and isomers makes the reaction poorly selective for synthesis.

A propagation step must regenerate a radical; a termination step removes radicals. Do not label Cl2_2 homolysis as propagation—it is the initiation step.

Topic 5: Alkenes

Syllabus
2017
Topic
—
Level
AS

An alkene double bond contains one sigma and one pi bond

An alkene is an unsaturated hydrocarbon containing a carbon–carbon double bond. An acyclic alkene with one C=C bond has general formula Cn_nH2n_{2n}; a cycloalkene also contains a ring, so a monocyclic species with one C=C has two fewer hydrogens, Cn_nH2n−2_{2n-2}.

Component Orbital overlap Electron-density location Consequence
σ\sigma bond head-on overlap along the internuclear axis directly between the carbon nuclei strong framework bond
π\pi bond sideways overlap of parallel p orbitals two regions above and below the C–C axis prevents free rotation and is exposed to electrophilic attack

The C=C consists of one σ\sigma bond and one π\pi bond. Addition reactions break the weaker π\pi component and form two new σ\sigma bonds, converting the two carbon centres from double-bonded to single-bonded.

A double bond is not two identical bonds. It contains one σ\sigma and one π\pi bond with different overlap and electron-density geometry.

Restricted C=C rotation creates geometric isomers

A π\pi bond requires parallel p orbitals. Rotation around C=C would destroy their sideways overlap, so rotation is restricted unless the π\pi bond is broken.

Geometric isomerism is possible only when each carbon of the C=C is bonded to two different substituents. The restricted arrangement then locks two different spatial patterns that cannot interconvert by simple rotation.

Alkene Groups on each double-bond carbon Geometric isomerism?
but-2-ene H/CH3_3 on both carbons yes
but-1-ene first carbon has H/H no
2-methylpropene one carbon has CH3_3/CH3_3 no

Restricted rotation is necessary but not sufficient. If either double-bond carbon has two identical substituents, swapping sides does not create a distinct isomer.

E/Z names compare the higher-priority groups

On each carbon of the C=C, rank the two attached atoms by atomic number: higher atomic number gives higher priority. If the directly attached atoms tie, compare the next set of attached atoms at the first point of difference.

Position of the two higher-priority groups Descriptor Memory aid
same side of C=C Z zusammen, together
opposite sides of C=C E entgegen, opposite

Draw the alkene with the C=C fixed, assign priority separately at its left and right carbon, then compare only the two higher-priority substituents. Place E or Z in parentheses before the complete IUPAC name.

Cis/trans works only when a suitable identical group occurs on both double-bond carbons. E/Z remains unambiguous when all four substituents differ, so it is the general naming system.

Do not choose the visually largest group. E/Z priority is determined by atomic number and the first point of difference, not mass of the whole substituent.

Alkenes undergo five required addition or oxidation reactions

Reagent and conditions Product type Example with ethene
H2_2, nickel catalyst, heat alkane CH2=CH2+H2→CH3CH3\mathrm{CH_2{=}CH_2+H_2 \rightarrow CH_3CH_3}
Cl2_2 or Br2_2 1,2-dihalogenoalkane CH2=CH2+Br2→CH2BrCH2Br\mathrm{CH_2{=}CH_2+Br_2 \rightarrow CH_2BrCH_2Br}
HCl or HBr monohalogenoalkane CH2=CH2+HBr→CH3CH2Br\mathrm{CH_2{=}CH_2+HBr \rightarrow CH_3CH_2Br}
steam, acid catalyst alcohol CH2=CH2+H2O→CH3CH2OH\mathrm{CH_2{=}CH_2+H_2O \rightarrow CH_3CH_2OH}
dilute acidified KMnO4_4 vicinal diol ethene forms HOCH2_2CH2_2OH

For an unsymmetrical alkene, H–X or H–OH can add in two orientations and may form more than one structural product. Product proportions depend on the relative stability of the possible carbocation intermediates.

In the mild oxidation test, purple manganate(VII) solution is decolourised as two –OH groups are added across C=C. In every listed reaction, the C=C π\pi bond is replaced by new σ\sigma bonds.

Hydration with steam makes an alcohol; acidified manganate(VII) makes a diol under the specified mild conditions. Do not treat these as the same addition reagent.

Bromine decolourisation tests for C=C

Shake the sample with bromine or bromine water at room temperature. An alkene rapidly changes the orange bromine colour to colourless because Br2_2 adds across the C=C bond.

For ethene: CH2=CH2+Br2→CH2BrCH2Br\mathrm{CH_2{=}CH_2 + Br_2 \rightarrow CH_2BrCH_2Br}. The product is 1,2-dibromoethane and no C=C remains.

Compare with a blank if the sample itself is coloured, use small quantities and avoid confusing dilution with reaction. Under these conditions, a saturated alkane does not rapidly decolourise bromine without ultraviolet initiation.

The observation detects reactive unsaturation such as C=C; it does not by itself identify the alkene's chain length or double-bond position.

Electrophilic addition follows electron-pair arrows and carbocations

A full curly arrow starts at an electron pair—a bond or lone pair—and points to where that pair forms a new bond. The alkene π\pi bond is electron-rich and attacks an electrophilic, δ+\delta+ atom.

Reaction First step Intermediate and second step
ethene + Br2_2 the π\pi electrons induce Brδ+^{\delta+}–Brδ−^{\delta-}; arrow C=C to Brδ+^{\delta+} and arrow Br–Br to Brδ−^{\delta-} a carbocation and Br−^- form; a Br−^- lone pair attacks C+^+ to give 1,2-dibromoethane
ethene + HBr label Hδ+^{\delta+}–Brδ−^{\delta-}; arrow C=C to H and arrow H–Br to Br ethyl carbocation and Br−^- form; Br−^- attacks C+^+ to give bromoethane
propene + HBr protonation can give a primary or secondary carbocation the more stable secondary carbocation forms more readily; Br−^- attack gives 2-bromopropane as major product

Carbocation stability follows tertiary > secondary > primary because surrounding alkyl groups stabilise the positive centre. This explains major-product proportions; it is evidence for the carbocation pathway.

A non-polar halogen still reacts because the electron-rich π\pi bond distorts its electron cloud and induces a dipole. Product distributions from unsymmetrical alkenes support intermediates of different stability.

Curly arrows must not start from a positive charge or from empty space. Use full two-electron arrows here, not the half-arrows used for free radicals.

Addition polymerisation opens C=C into a repeat unit

In addition polymerisation, many alkene monomers join when their C=C π\pi bonds open. No small molecule is eliminated; the monomer atoms are conserved in the polymer chain.

Direction Procedure
monomer to repeat unit replace C=C by C–C; keep every substituent on its original carbon; place the two-carbon segment in brackets with extension bonds crossing both sides; write subscript nn
repeat unit to monomer identify the two backbone carbons inside one repeat; remove the extension bonds and restore C=C between those carbons; retain all substituents

Propene, CH2_2=CHCH3_3, gives repeat unit [–CH2_2–CH(CH3_3)–]n_n. Chloroethene, CH2_2=CHCl, gives [–CH2_2–CHCl–]n_n.

The repeat bracket must enclose exactly one repeating connectivity unit, show bonds continuing through both bracket edges, and preserve the monomer's atom count and substituent placement.

Do not leave a C=C in an addition-polymer repeat unit, and do not add or remove H atoms or a small-molecule product.

Polymer disposal needs degradable materials and cleaner incineration

Strategy How it limits the problem Limitation to manage
develop biodegradable polymers microorganisms, water or environmental conditions break susceptible links so waste persists for less time degradation requires suitable conditions and products must be acceptably non-toxic
remove toxic incineration gases scrub acidic gases with alkaline material; use filters or other gas-cleaning stages before flue gases are released equipment and reagents are required, and captured residues still need safe disposal

Many addition polymers have strong, chemically unreactive carbon backbones and persist in landfill or the environment. Incineration reduces waste volume and can recover energy, but some polymers or additives can produce harmful gases if emissions are untreated.

A useful disposal decision considers the polymer composition, collection route, actual degradation environment, energy recovery and the emissions and residues from treatment rather than relying on one label.

Biodegradable does not mean that a polymer disappears immediately in every environment. Incineration does not remove pollution unless toxic waste gases are captured or converted before release.