Carbon and its Compounds Class 10 Science Notes

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  • Bonding in carbon: Carbon contain 4 electron in outermost shell. It requires large energy to donate 4 electrons and attain stability or noble gas configuration. Hence, carbon share its electron forming covalent bond.
  • Types of covalent bond:
    • Single covalent bond: Bond formed by sharing of two electrons. E.g. methane.
    • Double covalent bond: Bond formed by sharing of four electrons. E.g ethene.
    • Triple covalent bond: Bond formed by sharing of six electrons. E.g. ethyne.
  • Allotropes of carbon: Carbon occur in different forms like diamond, graphite and fullerenes.

Allotropes of carbon

Bonding

Structure

Physical property

Electrical conduction

Diamond

Each carbon bonded with 4  other carbon

  

Very hard

No conduction

Graphite

Each carbon bonded to 3 other carbon in same plane

 

Soft, slippery, easily breakable

Good Conductor

Fullerenes

In fullerene C-60, carbon atoms are arranged in football like structure  

   

Soft and slippery

Bad Conductor

  • Nature of carbon:
    • Carbon has ability to form long chain of carbon atoms. This is known as property of catenation.
    • Carbon compound can be straight chain, branched chain or can be in ring structure.
    • Carbon compounds are linked with single, double and triple bond. Carbon compounds with single bond are saturated compounds. Carbon compounds with double or triple bonds are unsaturated compounds.
    • Valency of carbon is four, hence it can form bond with four carbon or other four elements. Each compound differs in physical and chemical properties. E.g. diamond is hard/ solid while methane(CH4) is gas.
  • Saturated Carbon Compound: They are linked with single bond. Single bond between carbon carbon can be represented by dash or by electron dot structure.
  • Unsaturated Carbon Compounds: They are linked with double or triple bond. Carbon carbon bonding can be represented by double dash  or triple dash in a dash structure or by electron dot structure.   
  • Chains, Branches and Rings: Carbon compounds contains long straight chain of atoms, or branch of carbon atom in chain or ring like structure.Carbon atom with same molecular formula and different structural formula are structural isomers. Chain / Branch / Rings may be saturated or unsaturated.
  • Hydrocarbons: Compounds containing carbon and hydrogen.

Hydrocarbon

Bond

Known as / General formula

Example

Saturated

Single bond

Alkanes   /   (CnH2n+2)

Methane, ethane, propane,etc.

Unsaturated

Double bond

Alkenes   /   (CnH2n)

Ethene, propene, butene, etc.

 

Triple bond

Alkynes   /   (CnH2n-2)

Ethyne, propyne, butyne, etc.

  • Other Carbon Compounds: other than hydrogen carbon forms bonds with oxygen, nitrogen, sulphur and halogens(Fluorine, Chlorine, Bromine, Iodine). Elements replacing hydrogen atoms are called heteroatom. It gives specific properties to carbon compound, hence are called functional group (Alcohol -OH, Halo -Cl/-Br/-I, Ketone  -CO, Carboxylic Acid -COOH).
  • Homologous series: Series of compound having same functional group.     
  • Nomenclature of Carbon Compounds:  [Refer the video to understand in detail]
      1. Select longest chain of carbon atoms and identify the parent alkane.

CH3-CH2-CH2-CH2-OH.  Parent alkane: butane

      1. Identify the functional group.

CH3-CH2-CH2-CH2OH.     Functional group: Alcohol i.e. OH (-ol)

      1. Number the carbon atom in chain such that, carbon atom attached to functional group gets lowest number.

   

      1. Name the compound by replacing ‘e’ of  parent alkane with name of functional group.

CH3-CH2-CH2-CH2OH Compound name: butanol

      1. Compound name should indicate position of functional group.

Compound name: butan-1-ol

      1. For unsaturated chain, ‘ane’ is replaced by  ‘ene’ or ‘yne’ according to the bond. E.g. propyne, butyne, hexene.
      2. Some functional groups are:

Functional groups

Prefix / Suffix

Halogen

Prefix: chloro- , bromo- , etc

Alcohol

Suffix: -ol

Aldehyde

Suffix: -al

Ketone

Suffix: -one

Carboxylic Acid

Suffix: -oic acid

Alkenes

Suffix: -ene

Alkynes

Suffix: -yne

  • Chemical properties of carbon compounds:
    • Combustion: Produces carbon dioxide and releases heat and light.
      1. Saturated hydrocarbons: Burns with clean blue flame.
      2. Unsaturated hydrocarbons: Burns with yellow flame and black smoke.    
    1. Formation of coal and petroleum: coal , petroleum are obtained from fossils, they are known as fossil fuels. Form by following process.  
    2. Oxidation: Ethanol is oxidised in presence of heat and potassium permanganate or acidified potassium dichromate to form acetic acid.

         

    • Addition Reaction: Unsaturated hydrocarbon are converted to saturated hydrocarbon by addition of hydrogen in presence of Nickel or Palladium catalyst. E.g. vegetable oil converted to saturated hydrocarbon.
    • Substitution Reaction: One atom or group of atoms replaced with another.
  •  Ethanol:

Properties

  • Liquid at room temperature
  • Good solvent
  • Soluble in water

Uses

  • Used in alcoholic drinks
  • Used in medicines (tincture iodine, cough syrups, tonics)
  • Used as additive to petrol

Effects

  • Pure ethanol if consumed causes harmful effects on body
  • Disturbs metabolic processes
  • Lack of coordination by mind

Reaction

  • Reaction with sodium releases hydrogen gas.

          

  • Dehydration of ethanol produces ethene.

           

  • Ethanoic acid / Acetic acid:

Properties

  • Weak acid
  • Freezes below 290 K (also called glacial acetic acid)
  • It is carboxylic acid

Uses

  • Used as preservatives in form of vinegar(5-8% of acetic acid).

Reactions

  • Esterification reaction:

          

  • Saponification Reaction:

          

  • On reaction with base forms salt and water.
  • Carbonates and Hydrogen Carbonates:

          

          

  • Soap: Soap is sodium or potassium salt of carboxylic acid. Molecules of soap have two ends hydrophilic end (Na+ / K+) and hydrophobic end (long chain of carboxylic acid). Dirt is oily in nature hence, the hydrophobic end dissolves it and orient inward, whereas, the hydrophilic end is oriented away from dirt. Hence, a micelle structure is formed.  Due to ion ion repulsion micelles don’t come together, and can be easily rinsed with water.
  • Detergent: In hard water, soap do not produce lather, but it forms precipitate with calcium and magnesium salts from water. Detergents are ammonium or sulphonate salts of carboxylic acids which are effective in hard water and do not form precipitate. They are used to make shampoos and products for cleaning clothes.