Chemical Properties of Carbon Compounds Explore the reactions that make carbon the king of chemistry.

What Are Chemical Properties?

Chemical Property

A chemical property tells how a substance reacts to create new substances. It contrasts with a physical property, which can be seen without altering the substance’s identity. Carbon compounds display their chemical properties in reactions like combustion, oxidation, addition and substitution.

Remember: chemical ≠ physical — one changes composition, the other doesn’t.

Source: NCERT Class 10 Science

Combustion Reaction

Combustion

A carbon compound rapidly combines with oxygen, releasing heat and light to form carbon dioxide and water.

Key Characteristics:

  • Needs excess \(O_2\)
  • Highly exothermic—gives heat & light
  • Products: \(CO_2\) and \(H_2O\)

Example:

\( \text{Hydrocarbon} + O_2 \rightarrow CO_2 + H_2O + \text{energy} \)

Complete vs Incomplete Combustion

Diagram showing blue (complete) and yellow (incomplete) flames with CO₂ test setup

Blue flame = complete; yellow, sooty flame = incomplete; lime-water test confirms CO₂.

Oxygen supply decides flame colour and products

Complete combustion: hydrocarbon burns with plenty of O₂, giving a clean blue flame and only CO₂ + H₂O.

Incomplete combustion: limited O₂ causes a yellow luminous flame, forming toxic CO and black carbon soot.

Key Points:

  • Blue, non-luminous flame + clear glassware → complete combustion observed.
  • Yellow flame, soot deposit, possible CO detector alert → incomplete combustion.
  • Bubble exhaust through lime water; milky precipitate confirms CO₂ from complete combustion.

Oxidation Reaction

Oxidation

In carbon compounds, oxidation means adding oxygen or removing hydrogen from the molecule, usually using a strong oxidising agent.

Key Characteristics:

  • Alkaline KMnO₄ (purple) supplies nascent oxygen.
  • Acidified K₂Cr₂O₇ (orange) is another common oxidiser.

Example:

\( \mathrm{CH_3CH_2OH + [O] \rightarrow CH_3COOH + H_2O} \)

Oxidation of Ethanol to Ethanoic Acid

Follow these ethanol oxidation steps to obtain ethanoic acid using alkaline \( \mathrm{KMnO_4} \).

1

Prepare Alkaline Mixture

Mix ethanol with dilute NaOH and add alkaline \( \mathrm{KMnO_4} \) slowly until the purple colour just disappears.

2

Gentle Heating

Heat the solution gently in a water bath to provide energy without evaporating ethanol.

3

Oxidation Reaction

Under heat, \( \mathrm{KMnO_4} \) oxidises ethanol to acetaldehyde and finally to ethanoic acid.

4

End-Point Observation

Persistent pale pink shows excess oxidant; stop heating and cool to collect ethanoic acid.

Pro Tip:

Always keep the mixture alkaline; acidic conditions reduce \( \mathrm{KMnO_4} \) before full oxidation occurs.

Addition Reaction

Addition Reaction

Two atoms or groups add across a carbon-carbon multiple bond, converting an unsaturated hydrocarbon into a saturated one.

Key Characteristics:

  • Needs a C=C or C≡C multiple bond.
  • Reactants join; no by-product is released.
  • Product becomes a saturated hydrocarbon.

Example:

CH2=CH2 + H2 → CH3–CH3  (hydrogenation of ethene).

Hydrogenation of Vegetable Oil

Illustration of hydrogen gas bubbling through oil with nickel catalyst leading to solid fat

Hydrogen gas + nickel converts liquid oil to solid fat.

Addition Reaction in Daily Life

Unsaturated vegetable oils contain C=C bonds that undergo hydrogenation, an addition reaction.

Industrially, hot oil is treated with hydrogen under pressure; finely divided nickel catalyses its conversion into semi-solid ghee or margarine.

Key Points:

  • Industrial application: large-scale production of ghee and margarine.
  • Nickel catalyst speeds the addition of H₂ and is recovered for reuse.
  • Shows how chemical addition reactions impact everyday food.

Substitution Reaction

Substitution Reaction

An atom or group in a saturated compound is replaced by another atom or group.

Key Characteristics:

  • Typical of alkanes because they are saturated.
  • Usually involves halogens such as Cl2 or Br2.
  • Requires UV light or high heat to start the reaction.

Example:

CH4 + Cl2   UV light → CH3Cl + HCl

Mechanism: Chlorination of Methane

Free-radical chain reaction. Initiation: UV splits Cl₂ to Cl•. Propagation: Cl• successively replaces H, forming CH₃Cl → CH₂Cl₂ → CHCl₃ → CCl₄ while regenerating radicals. Termination: radicals combine and stop the chain.

Initiation
Cl₂ → 2Cl•
CH₄
CH₃Cl
CH₂Cl₂
CHCl₃
CCl₄
Termination

Legend:

Start/End
Decision
Process

Addition vs Substitution

Addition Reactions

Need unsaturated compounds: alkenes or alkynes.
π bond breaks; two atoms/groups attach across it.
Product becomes more saturated than reactant.

Substitution Reactions

Occur in saturated compounds like alkanes or benzene.
One atom/group replaces another; carbon framework stays.
Often proceeds via free-radical, electrophilic or nucleophilic paths.

Key Similarities

Both involve breaking and forming covalent bonds.
Both convert reactants into new, useful products.

Multiple Choice Question – Formative Assessment

Question

Which type of reaction converts an unsaturated hydrocarbon into a saturated hydrocarbon?

1
Addition reaction
2
Substitution reaction
3
Oxidation reaction
4
Combustion reaction

Hint:

The reaction adds atoms across the carbon–carbon multiple bond.

Classify the Reactions

Drag each reaction into the box that matches its type: Combustion, Oxidation, Addition, or Substitution.

Draggable Items

CH₄ + 2O₂ → CO₂ + 2H₂O
CH₃CH₂OH + [O] → CH₃CHO + H₂O
CH₂=CH₂ + H₂ → CH₃CH₃
CH₄ + Cl₂ → CH₃Cl + HCl
CH₃CHO + [O] → CH₃COOH
CH₂=CH₂ + Cl₂ → CH₂Cl–CH₂Cl
C₂H₆ + Br₂ → C₂H₅Br + HBr
C₂H₅OH + 3O₂ → 2CO₂ + 3H₂O

Drop Zones

Combustion

Oxidation

Addition

Substitution

Tip:

Look for what is added, removed, or swapped in the organic molecule.

Key Takeaways

Combustion yields heat, light, \( \mathrm{CO_2} \) and \( \mathrm{H_2O} \).

Oxidation adds oxygen or strips hydrogen from the molecule.

Addition attaches atoms across a double or triple bond.

Substitution swaps an atom in a saturated chain with another.

Together these reactions summarise the chemical behaviour of carbon compounds.

Collage of reaction icons summarising each type

Thank You!

We hope you found this lesson informative and engaging.