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Revision: Carbon and its Compounds Science English Medium Class 10 CBSE

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Definitions [25]

Definition: Covalent Molecule

The molecule formed due to the sharing of electrons (covalent bond) is called a covalent molecule.

Definition: Covalent Compound

The chemical bond that is formed between two combining atoms by mutual sharing of one or more pairs of electrons is called a covalent (or a molecular) bond, and the compound formed due to this bond is called a covalent compound.

Define a coordinate bond.

The bond formed between two atoms by sharing a pair of electrons, provided entirely by one of the combining atoms but shared by both, is called a coordinate bond. 

Define a covalent bond.

The chemical bond formed between two combining atoms by mutual sharing of one or more pairs of electrons is called a covalent bond.

Define Allotrophy

When an element possess 2 or more different forms in the same state, they are called allotropes and the phenomenon is known as allotropy. Diamond and graphite are the 2 allotropes of carbon.

Define the following:

Adsorption

Adsorption is the property due to which a substance absorbs gases, liquids and solids on its surface.

Define the following:

Carbonization

The process of the slow conversion of vegetable matter into carbon-rich substances is called carbonization.

Define catenation.

Carbon possesses a unique property of combining with other carbon atoms to form long chains. This property is called catenation. The chains can be straight, branched or closed.

The self-linking property of atoms of an element to form very long straight or branched chains and cyclic rings is known as catenation. This property is shown by carbon whose small size and tetravalency helps it to form large structures by self-linking.

Definition: Tetravalency of Carbon

The characteristic of the carbon atom, by virtue of which it forms four covalent bonds, is called the tetravalency of carbon.

Definition: Catenation

The property of self-linking of atoms of an element through covalent bonds in order to form straight chains, branched chains and cyclic chains of different sizes is known as catenation.

Definition: Organic Compounds

Organic compounds are the compounds of carbon.

Define of chain isomerism.

When two or more compounds have a similar molecular formula but are different in the arrangement of carbon atoms in straight or branched chains, the compounds are referred to as chain isomers.

Define isomerism.

Compounds having the same molecular formula but different structural formulas are called isomers and the phenomenon is called isomerism.

Define a functional group.

An atom or a group of atoms attached to an alkyl group, which takes part in most of the chemical reactions, is called a functional group or functional radical.

Definition: Unsaturated Carbon Compounds

The compounds of carbon having double or triple bonds between the carbon atoms are known as unsaturated carbon compounds.

Definition: Saturated Compounds

The valencies of all the atoms are satisfied by single bonds between them. Such carbon compounds are called saturated compounds.

Definition: Functional Groups

The heteroatoms and the group containing these confer specific properties to the compound, regardless of the length and nature of the carbon chain and hence are called functional groups.

Definition: Alkanes

The saturated hydrocarbons are called alkanes.

Definition: Alkenes

The unsaturated hydrocarbons which contain one or more double bonds are called alkenes.

Definition: Alkynes

Those containing one or more triple bonds are called alkynes.

Definition: Structural Isomers

Compounds with identical molecular formula but different structures are called structural isomers.

Definition: Hydrocarbons

The carbon compounds which contain only carbon and hydrogen are called hydrocarbons.

Define Homologous series.

A series of compounds with similar chemical properties, in which members differ from one another by an additional CH2 group, is called a homologous series.

Definition: Homologous Series

The same functional group substitutes for hydrogen in a carbon chain is called a homologous series.

OR

A homologous series is a group of organic compounds having  similar structure and similar chemical properties in which the successive compounds differ by a CH2 group.

OR

The series of compounds formed by joining the same functional group in the place of a particular hydrogen atom on the chains having sequentially increasing length is called homologous series.

Definition: Nomenclature

Nomenclature is the system of assignment of names to organic compounds.

Formulae [1]

Give the general formula of carboxylic acids.

CnH2n+1COOH (or RCOOH)

Key Points

Key Points: The Covalent Bond
  • Carbon forms covalent bonds by sharing electrons to achieve a noble gas configuration.
  • Covalent bonds can be single, double, or triple, as seen in molecules like H₂, O₂, and N₂.
  • Covalent compounds have low melting and boiling points and are poor conductors of electricity.
  • Carbon has allotropes such as diamond, graphite, and fullerene (C₆₀), each with different physical properties.
Key Points: Carbon: A Versatile Element
  • Carbon forms many compounds, from simple ones like methane to complex ones like DNA, due to its bonding versatility.
  • Catenation allows carbon to form long chains or rings by bonding with itself.
  • Carbon forms single, double, and triple covalent bonds, leading to saturated and unsaturated compounds.
  • Being tetravalent, carbon forms four strong covalent bonds with elements like H, O, N, and Cl.
  • Isomerism increases the number of carbon compounds by allowing different structures with the same molecular formula.
 
Key Points: Organic Compounds
  • Specification: Organic chemistry studies carbon compounds (excluding CO₂, carbonates, etc.).
  • Sources: Found in plants, animals, coal, petroleum, wood, and by fermentation.
  • Lab Synthesis: Many organic compounds are made in labs today.
  • Daily Use: Found in soaps, clothes, fuels, medicines, food, etc.
  • Importance: Organic compounds are used in almost every part of life.
Key Points: Homologous Series
  • A homologous series is a group of compounds with the same functional group and similar chemical properties.
  • Successive members differ by one CH₂ (methylene) unit, increasing the molecular mass by 14 u.
  • All members of a homologous series follow the same general molecular formula (e.g., alkanes CnH2n+2).
  • Physical properties such as boiling and melting points show a gradual change with increasing molecular mass.
  • Knowing the properties of a few members helps predict the properties of other members in the series.
Key points: Nomenclature of Carbon Compounds
  • The IUPAC system provides a unique, systematic way to name carbon compounds based on structure, replacing confusing common names.
  • An IUPAC name has three parts: prefix, parent, and suffix, reflecting the carbon chain and functional group.
  • The parent name is based on the longest carbon chain, and its ending changes to –ane, –ene, or –yne depending on the number of bonds.
  • Functional groups are shown as prefixes or suffixes, and the chain is numbered to give them the lowest possible number.
  • If the suffix begins with a vowel, the final ‘e’ in the parent alkane name is dropped (e.g., propane → propanone).
Key Points: Combustion
  • Carbon compounds combust in oxygen to produce carbon dioxide, water (for hydrocarbons), heat, and light.
  • Hydrocarbons such as methane, ethanol, and propane undergo complete combustion, releasing energy.
  • Complete combustion is indicated by a clean, blue flame, while incomplete combustion produces a yellow, sooty flame.
  • Combustion is an important chemical property of carbon compounds, especially common fuels.
Key Points: Ethanol
  • Ethanol is a colourless liquid with a boiling point of 78 °C, soluble in water, and used in medicines, drinks, and as a clean-burning fuel (e.g., gasohol).
  • Ethanol reacts with sodium to form sodium ethoxide and hydrogen gas is evolved.
  • When heated with concentrated H₂SO₄ at 170 °C, ethanol undergoes dehydration to form ethene, an unsaturated compound.
  • Methanol is highly poisonous, and industrial ethanol is made unfit for drinking by mixing methanol and adding a blue dye (denatured spirit).
Key Points: Ethanoic Acid
  • Ethanoic acid (acetic acid) is a carboxylic acid; its 5–8% aqueous solution is vinegar, and it shows acidic nature by turning blue litmus red.
  • Pure ethanoic acid freezes at 17 °C (290 K), so it is called glacial acetic acid.
  • Being a weak acid, ethanoic acid is not completely ionised in aqueous solution.
  • Ethanoic acid reacts with bases, carbonates, and bicarbonates to form a salt, water, and CO₂ (CO₂ turns lime water milky).
  • It reacts with ethanol in the presence of conc. H₂SO₄ to form an ester (ethyl ethanoate) with a sweet smell (esterification).
Key Points: Soaps and Detergents
  • Soap molecules form micelles to trap and remove oily dirt.
  • Micelles have hydrophobic tails (oil-loving) and hydrophilic heads (water-loving).
  • Soap is less effective in hard water due to scum formation with Ca²⁺/Mg²⁺.
  • Detergents do not form scum and work well in both hard and soft water.
  • Soap and detergent solutions appear cloudy due to suspended micelles.

Important Questions [160]

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