Chapter 16

Introduction to Organic Chemistry

College
At a glance
Core ideaCarbon's four bonds and self-bonding build millions of compounds.
Key termFunctional group — the reactive site that sets a molecule's chemistry.
You can…Name hydrocarbon families and test for unsaturation with bromine water.
Watch outAlkanes substitute; alkenes add across the reactive C=C bond.
Theory

The chemistry of carbon

Organic chemistry is the chemistry of carbon compounds. Carbon's power comes from four features: it forms four covalent bonds, bonds strongly to itself (catenation) into chains and rings, forms single, double and triple bonds, and combines with H, O, N, and halogens — yielding millions of stable compounds.

The simplest are hydrocarbons (C and H only):

Hydrocarbon families
FamilyBondingGeneral formulaExample
AlkanesAll single (saturated)CnH2n+2ethane C₂H₆
AlkenesOne C=C double bondCnH2nethene C₂H₄
AlkynesOne C≡C triple bondCnH2n−2ethyne C₂H₂

A functional group is an atom or group that gives a molecule characteristic reactions — e.g. hydroxyl (–OH, alcohols), carboxyl (–COOH, carboxylic acids), amino (–NH₂, amines). Molecules with the same molecular formula but different arrangements are isomers.

Explanation

Families, homologous series and reactions

Organic chemistry is manageable because compounds fall into homologous series — families that share a functional group and a general formula, with each member differing from the next by a CH₂ unit. Members of a series show a smooth gradation in physical properties (boiling point rises with chain length) and, crucially, the same chemical reactions, because reactivity is dictated by the functional group, not the whole molecule. Learn the group, and you know the chemistry of the entire family.

Two reaction patterns are foundational. Saturated alkanes are relatively unreactive and undergo substitution (e.g. with halogens under UV light). Unsaturated alkenes, with their reactive C=C double bond, undergo addition — the double bond opens to take on a new atom or group across it. The bromine-water test exploits exactly this: alkenes decolourise orange bromine water by addition, alkanes do not, giving a simple lab test for unsaturation.

Practical

Worked example — combustion and an addition reaction

(a) Complete combustion of ethane. Balance C₂H₆ + O₂ → CO₂ + H₂O.

  1. Balance carbon: 2 C → 2 CO₂.
  2. Balance hydrogen: 6 H → 3 H₂O.
  3. Count oxygen on the right: 2(2) + 3(1) = 7 O atoms = 3.5 O₂.
  4. Clear the fraction by doubling every coefficient: 2C₂H₆ + 7O₂ → 4CO₂ + 6H₂O.
Step 1Balance CMatch carbon atoms first — set the CO₂ coefficient.
Step 2Balance HMatch hydrogen next — set the H₂O coefficient.
Step 3Balance OCount oxygen last, since it appears in both products.
Step 4Clear fractionsMultiply every coefficient through to remove any ½.

(b) Addition of bromine to ethene. The C=C bond opens and a Br adds to each carbon:

CH₂=CH₂ + Br₂ → CH₂Br–CH₂Br   1,2-dibromoethane
  1. Identify the reactive site: the electron-rich C=C double bond of ethene.
  2. The double bond breaks open, freeing two bonding positions.
  3. One bromine atom bonds to each carbon; no atoms are lost — this is addition, not substitution.
  4. Orange bromine water is decolourised, confirming an alkene (a positive unsaturation test).
Q&A
Draw and name the two structural isomers of C₄H₁₀.

Both have formula C₄H₁₀ but differ in carbon skeleton: butane (a straight chain, CH₃–CH₂–CH₂–CH₃) and 2-methylpropane / isobutane (a branched chain, a central CH with three CH₃ groups and one H). Same formula, different structure and slightly different properties.

How can you chemically distinguish ethane from ethene?

Add bromine water. Ethene (an alkene, C=C) decolourises the orange bromine water rapidly by addition. Ethane (a saturated alkane) does not react and the colour stays. Decolourisation is the classic test for unsaturation.

Why do alkanes undergo substitution but alkenes undergo addition?

Alkanes are saturated — every carbon already has four single bonds, so a new atom can only enter by replacing an existing atom (substitution). Alkenes have a reactive C=C double bond that can open up, letting atoms add across it without anything leaving (addition).

What functional group makes ethanol an alcohol, and what does it become on oxidation?

The hydroxyl group, –OH, defines alcohols. On mild oxidation ethanol (CH₃CH₂OH) is oxidised first to the aldehyde ethanal (CH₃CHO) and, on further oxidation, to the carboxylic acid ethanoic acid (CH₃COOH) — the acid in vinegar.

Concept mind map

How the ideas connect

Every key idea in this chapter, branching from the core concept — use it to see the whole picture at a glance.

Carbon bondingHydrocarbonsFunctional groupsHomologous seriesIsomersAddition reactionsOrganic Chemistry
Infographic

The key facts, visualised

Alkane
saturated hydrocarbon, general formula CnH2n+2
Alkene
has a C=C double bond, CnH2n
Isomers
same formula, different structure
CH4
methane, the simplest alkane
Solved examples

Worked problems, step by step

Follow each solution line by line, then try to reproduce it on paper before moving on.

Example 1Write the balanced combustion of methane, CH4.

  1. Products of complete combustion are CO2 and H2O.
  2. Balance carbon and hydrogen, then oxygen.
  3. This gives CH4 + 2O2 -> CO2 + 2H2O.

Example 2What forms when ethene reacts with bromine?

  1. Ethene, C2H4, has a C=C double bond that opens up.
  2. Bromine (Br2) adds across the double bond in an addition reaction.
  3. Each carbon gains a Br, forming 1,2-dibromoethane.
Practice problem set

Now you try

Work each one out first, then tap to reveal the worked answer.

1What is the general formula of an alkane?
CnH2n+2, for example ethane is C2H6.
2How can you test for a C=C double bond?
Add bromine water; it decolourises with an alkene by an addition reaction.
3What is a homologous series?
A family of compounds with the same general formula and similar properties, differing by CH2.
4What are structural isomers?
Compounds with the same molecular formula but different arrangements of atoms.
5Name the functional group in ethanol.
The hydroxyl group, -OH, which makes it an alcohol.
6Why is carbon able to form so many compounds?
It forms four strong covalent bonds and can make long chains and rings.