Carbon is a non-metal with the symbol C. All living things, including plants and animals, are made up of carbon-based compounds.
The atomic number of carbon is 6. Its electronic configuration is:
K Shell: 2 electrons
L Shell: 4 electrons (Valence Shell)
Fig. 1 — Bohr model of Carbon, showing 2 electrons in the K shell and 4 electrons in the L shell.
Carbon always forms covalent bonds to achieve a stable electron configuration.
Covalent Bonding
A covalent bond is a chemical bond formed when pairs of electrons are shared between two atoms. It is mostly formed between two identical nonmetallic atoms or between different nonmetallic atoms.
Examples of Covalent Bonding
1. Single Bond in Hydrogen (H₂)
A Hydrogen (H) atom needs one more electron to complete its outermost shell (duplet). Two hydrogen atoms share one pair of electrons to form a single covalent bond.
Fig. 2 — Formation of a single covalent bond in a Hydrogen (H₂) molecule.
2. Double Bond in Oxygen (O₂)
An Oxygen (O) atom needs two more electrons to complete its octet. Two oxygen atoms share two pairs of electrons to form a double covalent bond.
Fig. 3 — Formation of a double covalent bond in an Oxygen (O₂) molecule.
3. Triple Bond in Nitrogen (N₂)
A Nitrogen (N) atom needs three more electrons to complete its octet. Two nitrogen atoms share three pairs of electrons to form a triple covalent bond.
Fig. 4 — Formation of a triple covalent bond in a Nitrogen (N₂) molecule.
4. Covalent Bonding in Water (H₂O)
Oxygen needs two electrons to complete its octet, while each Hydrogen atom needs one. Therefore, one Oxygen atom shares one electron with each of two Hydrogen atoms, forming two single covalent bonds.
Fig. 5 — Formation of covalent bonds in a Water (H₂O) molecule.
Physical Properties of Covalent Compounds
Covalent compounds have low melting and boiling points because they have weak intermolecular forces.
They are generally poor conductors of electricity because electrons are shared between atoms, meaning no free-moving charged particles (ions) are formed.
The Versatile Nature of Carbon
How Carbon Attains Noble Gas Configuration
Carbon is tetravalent (it has 4 valence electrons). It does not form ionic bonds by either losing four electrons (to form C4+) or gaining four electrons (to form C4-).
It is difficult for the nucleus to hold four extra electrons.
It would require a very large amount of energy to remove four electrons.
Instead, carbon forms covalent bonds by sharing its four valence electrons with other atoms to attain a stable noble gas configuration.
Characteristic Properties of Carbon
Three characteristic properties of carbon lead to the formation of a vast number of compounds:
1. Catenation
Catenation is the unique self-linking property of an element, where atoms form long chains and rings by covalent bonds. Carbon exhibits this property to the maximum extent.
Fig. 6 — Catenation allows Carbon to form straight chains, branched chains, and ring structures.
2. Tetravalency
Carbon has 4 valence electrons, so it can form four covalent bonds. It can bond with four other carbon atoms, monovalent atoms (like H, Cl), or other atoms like Oxygen, Nitrogen, and Sulphur.
3. Tendency to form Multiple Bonds
Due to its small size, carbon has a strong tendency to form multiple bonds (double and triple bonds) by sharing more than one electron pair with its own atoms or with atoms of other elements like Oxygen and Nitrogen.
Allotropes of Carbon
Allotropy is the property by which an element exists in more than one form. Each form (allotrope) has different physical properties but similar chemical properties.
Diamond
In diamond, each carbon atom is covalently bonded to four other carbon atoms, forming a rigid 3-D tetrahedral structure.
It is the hardest known substance.
It is a bad conductor of electricity. This is because all four valence electrons of each carbon are used in covalent bonding, so no free electrons are left to move.
It has a very high melting point.
Uses: Making jewellery, cutting tools, and grinders.
Graphite
In graphite, each carbon atom is bonded to three other carbon atoms, forming hexagonal rings in flat layers (planes).
It is soft and slippery because these layers can slide over one another (held by weak van der Waals forces).
It is a good conductor of electricity. Because each carbon is only bonded to three others, the fourth valence electron is free to move between the layers.
Uses: Pencil "leads," lubricants, batteries, and cells.
Fig. 8 — The layered hexagonal structure of graphite.
Fullerene
Fullerenes form another class of carbon allotropes.
The first one identified was C-60, which has carbon atoms arranged in the shape of a football (a buckyball).
It consists of 12 pentagons and 20 hexagons.
Fig. 9 — The structure of Buckminsterfullerene (C-60).
Hydrocarbons
Compounds made up of only hydrogen and carbon are called hydrocarbons.
Saturated Hydrocarbons
These are compounds of carbon which are linked only by single bonds between the carbon atoms.
Alkanes
Alkanes are saturated hydrocarbons with only C-C single bonds.
General formula: CnH2n+2
Example: Ethane (C2H6)
Fig. 10 — Structural formula of Ethane (C2H6).
Unsaturated Hydrocarbons
These are compounds of carbon having double or triple bonds between their carbon atoms.
Alkenes
Alkenes are unsaturated hydrocarbons with at least one C=C double bond.
General formula: CnH2n
Example: Ethene (C2H4)
Fig. 11 — Structural formula of Ethene (C2H4).
Alkynes
Alkynes are unsaturated hydrocarbons with at least one C≡C triple bond.
General formula: CnH2n-2
Example: Ethyne (C2H2)
Fig. 12 — Structural formula of Ethyne (C2H2).
Nomenclature
IUPAC Nomenclature of Hydrocarbons
Formula: Name of Hydrocarbon = Prefix + Suffix
Prefix (Root Word)
The prefix is based on the number of carbon atoms in the main chain.
No. of Carbons
Prefix
No. of Carbons
Prefix
1
Meth-
6
Hex-
2
Eth-
7
Hept-
3
Prop-
8
Oct-
4
But-
9
Non-
5
Pent-
10
Dec-
Suffix (Bond Type)
The suffix is based on the type of bond between carbon atoms.
-ane for Single Bond (Alkanes)
-ene for Double Bond (Alkenes)
-yne for Triple Bond (Alkynes)
Examples:
CH3-CH2-CH3: 3 Carbons (Prop-) + Single Bonds (-ane) = Propane
CH3-CH=CH2: 3 Carbons (Prop-) + Double Bond (-ene) = Propene
CH3-C≡CH: 3 Carbons (Prop-) + Triple Bond (-yne) = Propyne
Step 1: Identify the number of carbon atoms in the longest continuous chain. This gives the Root Word (Meth, Eth, Prop, etc.).
Step 2: Identify the type of C-C bond (single, double, triple). This gives the primary Suffix (-ane, -ene, -yne).
Step 3: Identify the functional group. This gives the main Suffix (-ol, -al, -oic acid) or a Prefix (Chloro-, Bromo-).
Chapter 7: Homologous Series
A homologous series is a series of carbon compounds in which the same functional group substitutes for hydrogen and successive members differ by a CH2 group.
Example (Alcohols):CH3OH (Methanol), C2H5OH (Ethanol), C3H7OH (Propanol)...
Properties of a Homologous Series
All members are represented by the same general formula.
Any two adjacent members differ by one carbon atom and two hydrogen atoms (a -CH2 group).
Any two adjacent members differ by a molecular mass of 14u.
All members show similar chemical properties (due to the same functional group).
Physical properties (like melting point, boiling point) show a gradual change as molecular mass increases.
Chemical Properties of Carbon Compounds
1. Combustion
Combustion is a chemical reaction in which a substance burns in oxygen to give out heat and light.
C + O2→CO2 + Heat + Light
CH4 + 2O2→CO2 + 2H2O + Heat + Light
CH3CH2OH + 3O2→2CO2 + 3H2O + Heat + Light
2. Oxidation
Alcohols can be converted to carboxylic acids in the presence of an oxidizing agent, such as alkaline KMnO4 (potassium permanganate) or acidified K2Cr2O7 (potassium dichromate).
CH3CH2OH + [O]→CH3COOH(Alkaline KMnO4)
💡 A catalyst is a substance that makes a chemical reaction happen faster (or occur at a lower temperature) without being used up in the reaction. Examples include Nickel (Ni), Palladium (Pd), and KMnO4.
3. Addition Reaction (Hydrogenation)
Unsaturated hydrocarbons (alkenes/alkynes) add hydrogen in the presence of a catalyst (like Ni or Pd) to give saturated hydrocarbons (alkanes). This is called a hydrogenation reaction.
Esters are sweet-smelling substances, used in making perfumes and as flavouring agents.
2. Saponification Reaction:
An ester reacts with a base (like NaOH) to form an alcohol and the sodium salt of the carboxylic acid (which is soap).
3. Reaction with Base (Neutralisation):
CH3COOH + NaOH→CH3COONa (Sodium acetate) + H2O
4. Reaction with Carbonates and Hydrogen Carbonates:
2CH3COOH + Na2CO3→2CH3COONa + H2O + CO2
CH3COOH + NaHCO3→CH3COONa + H2O + CO2
Test to Distinguish Ethanol & Ethanoic Acid:
Add sodium carbonate (Na2CO3) to both samples. Ethanoic acid will react to produce CO2 gas (brisk effervescence), which turns lime water milky. Ethanol will not react.
Soaps and Detergents
Soap
A soap is the sodium or potassium salt of a long-chain carboxylic acid (fatty acid). Example: C17H35COO-Na+ (Sodium stearate).
A soap molecule has two parts:
An ionic, hydrophilic part (water-loving) - the COO-Na+ head.
A long hydrocarbon chain, which is hydrophobic (water-repelling) - the tail.
Fig. 15 — The structure of a soap molecule, showing the hydrophilic head and hydrophobic tail.
Cleansing Action of Soap
Most dirt is oily (non-polar) and does not dissolve in water (polar).
When soap is added to water, the soap molecules form clusters called micelles.
In a micelle, the hydrophobic tails point inwards, dissolving the oil or dirt particle.
The hydrophilic heads point outwards, remaining in contact with the water.
This forms an emulsion. When the fabric is agitated (scrubbed) or rinsed, the micelles containing the dirt are lifted away and washed away with the water.
Fig. 16 — Cleansing action of soap. The micelle traps the oily dirt, allowing it to be washed away by water.
Detergents
Detergents are generally ammonium or sulphonate salts of long-chain carboxylic acids. They have a similar cleansing action to soaps.
Hard Water and Scum
Hard water contains dissolved minerals, specifically calcium (Ca2+) and magnesium (Mg2+) ions.
When soap is used in hard water, the Ca2+ and Mg2+ ions react with the soap molecules to form an insoluble product called scum. This scum sticks to the clothes and prevents effective cleaning.
Detergents do not form insoluble scum with hard water. The calcium and magnesium salts of detergents are soluble in water.
💡 Key takeaway: Detergents are effective in both soft and hard water, while soaps are effective only in soft water.